研究者業績

松下 一之

マツシタ カズユキ  (Kazuyuki Matsushita)

基本情報

所属
千葉大学 医学部附属病院 検査部長 (診療教授)
(兼任)千葉大学病院がんゲノムセンター 診療教授
学位
医学博士(1980年3月 千葉大学)

J-GLOBAL ID
200901032768211652
researchmap会員ID
5000043159

外部リンク

論文

 340
  • Kazuyuki Matsushita, Takayuki Ishige, Kousuke Watanabe, Toshiaki Akahane, Akihide Tanimoto, Michiko Yoshimoto, Munekazu Yamakuchi, Teruto Hashiguchi, Yoshinaga Okugawa, Makoto Ikejiri, Toshikazu Yamaguchi, Tadashi Yamasaki, Mayu Takeda, Masaaki Hibi, Naoki Akiyama, Kaho Shimizu, Naonori Hashimoto, Hiroko Sato, Yoshinori Tanaka, Fumie Amari, Kaname Nakatani, Shuji Tohda, Satoko Nakajo, Yo Niida, Hirotaka Matsui
    Scientific Reports 15(1) 2025年1月7日  
  • 土田 知央, 宮部 安規子, 瀬川 俊介, 鈴木 眞, 山下 晃司, 藤川 樹, 川崎 健治, 松下 一之
    千臨技会誌 (144) 51-53 2025年1月  
    症例は70歳代女性。悪寒、嘔吐、食思不振、発熱から急性胆嚢炎が疑われ、当院消化器内科に緊急入院した。入院時血液培養のうち、嫌気ボトルが培養44時間で陽転し、アネロコロンビアウサギ血液培地(日本BD)での培養で、極微小の透明なコロニーが観察され、質量分析と16S rRNA遺伝子解析によってDialister pneumosintesと同定された。本菌はVeillonella科に属し、腸管、口腔内、腟などに常在する偏性嫌気性グラム陰性桿菌である。Dialister属はヒトに対する病原性については不明な点が多い。本菌の症例報告は2002年から2023年の間で、国内外から12報14症例とまれである。本菌は発育が遅く、全自動同定感受性装置の同定可能菌種に含まれておらず、現状は質量分析や16S rRNA遺伝子解析による同定のみのために症例報告数が少ないことが予想される。今後はより多くの症例情報を蓄積し、ヒトへの病原性の有無や薬剤感受性検査法の確立を行うことが必要である。(著者抄録)
  • 鈴木 眞, 村田 正太, 菅原 庸, 荒井 千夏, 松浦 佑介, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 山下 晃司, 藤川 樹, 川崎 健治, 菅井 基行, 大鳥 精司, 松下 一之
    日本臨床微生物学会雑誌 35(Suppl.1) 303-303 2024年12月  
  • 山下 晃司, 伴 さやか, 矢口 貴志, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 堀田 恵海, 鈴木 眞, 菅谷 陸, 土田 知央, 村田 正太, 川崎 健治, 松下 一之
    日本臨床微生物学会雑誌 35(Suppl.1) 305-305 2024年12月  
  • Misuzu Yahaba, Haruna Asano, Kengo Saito, Shota Murata, Kenji Kawasaki, Hitoshi Chiba, Shou Yokota, Hiroshi Yoshikawa, Yoriko Herai, Kazutaka Yamagishi, Yuki Shiko, Kazuyuki Matsushita, Hideki Hanaoka, Toshibumi Taniguchi, Koutaro Yokote, Hiroshi Nakajima, Eiji Ido, Hidetoshi Igari
    Japanese journal of infectious diseases 2024年11月29日  
    The effect of antibodies elicited by bivalent mRNA vaccines (original and omicron BA.1) on preventing coronavirus disease 2019 (COVID-19) onset in the presence of the XBB variant remains unknown. A prospective cohort study conducted at Chiba University Hospital examined healthcare workers who received their sixth vaccination with the Pfizer-BioNTech COVID-19 bivalent mRNA vaccine (original and omicron BA.1). Researchers quantitatively measured serum anti-spike (S) antibody levels. Participants not infected during the 60-day observation period after vaccination had significantly higher S antibody titers than those who were newly infected (27756 U/mL, 95% CI [24988-30831 U/mL] vs. 15321 U/mL, 95% CI [10824-21688 U/mL], p<0.05). The risk of infection decreased by 84% when the S antibody titer exceeded 15500 U/ml. Neutralizing antibody titers against the XBB.1.16 and XBB.1.42 variants were higher in age- and sex-matched noninfected individuals than in newly infected individuals during the post-vaccination observation period. S antibody titers were highly correlated with neutralizing antibody titers. In conclusion, after the sixth COVID-19 vaccination with the bivalent mRNA vaccine (original and omicron BA.1), high S antibody titers correlated with disease prevention, even in the presence of XBB variants.
  • Yuriko Yamazaki, Tomoka Ito, Seitaro Nakagawa, Takashi Sugihira, Chinami Kurita-Tachibana, Amer E. Villaruz, Kensuke Ishiguro, Barbora Salcman, Shuo Li, Sanami Takada, Naohiro Inohara, Yoko Kusuya, Aki Shibata, Masakazu Tamai, Reika Aoyama, Kanako Inoue, Shota Murata, Kazuyuki Matsushita, Akiko Miyabe, Toshibumi Taniguchi, Hidetoshi Igari, Naruhiko Ishiwada, Masateru Taniguchi, Taka-Aki Nakada, Hiroyuki Matsue, Manabu Fujimoto, Haruka Hishiki, Yoshiteru Osone, Hiromichi Hamada, Naoki Shimojo, Tsutomu Suzuki, Michael Otto, Gabriel Núñez, Hiroki Takahashi, Akiko Takaya, Yuumi Nakamura
    Nature Communications 15(1) 2024年11月7日  
  • Jun Ikari, Megumi Katsumata, Akira Urano, Takuro Imamoto, Yuri Suzuki, Akira Nishiyama, Hajime Yokota, Kojiro Ono, Kentaro Okamoto, Eriko Abe, Tomoko Kamata, Shota Fujii, Kenichiro Okumura, Joji Ota, Eiko Suzuki, Naoko Kawata, Yoshihito Ozawa, Yoshitada Masuda, Kazuyuki Matsushita, Seiichiro Sakao, Takashi Uno, Koichiro Tatsumi, Takuji Suzuki
    BMJ open respiratory research 11(1) 2024年8月5日  
    INTRODUCTION: To date, there is limited evidence on the effects of bronchodilators on respiratory dynamics in chronic obstructive pulmonary disease (COPD). Dynamic chest radiography (DCR) is a novel radiographic modality that provides real-time, objective and quantifiable kinetic data, including changes in the lung area (Rs), tracheal diameter, diaphragmatic kinetics and pulmonary ventilation during respiration, at a lower radiation dose than that used by fluoroscopic or CT imaging. However, the therapeutic effect of dual bronchodilators on respiratory kinetics, such as chest wall dynamics and respiratory muscle function, has not yet been prospectively evaluated using DCR. AIM: This study aims to evaluate the effects of bronchodilator therapy on respiratory kinetics in patients with COPD using DCR. METHODS AND ANALYSIS: This is an open-label, prospective, single-centre, non-controlled, comparative study. A total of 35 patients with COPD, aged 40-85 years, with a forced expiratory volume in the first second of 30-80%, will be enrolled. After a 2-4 weeks washout period, patients will receive tiotropium/olodaterol therapy for 6 weeks. Treatment effects will be evaluated based on DCR findings, pulmonary function test results and patient-related outcomes obtained before and after treatment. The primary endpoint is the change in Rs after therapy. The secondary endpoints include differences in other DCR parameters (diaphragmatic kinetics, tracheal diameter change and maximum pixel value change rate), pulmonary function test results and patient-related outcomes between pre-therapy and post-therapy values. All adverse events will be reported. ETHICS AND DISSEMINATION: Ethical approval for this study was obtained from the Ethics Committee of Chiba University Hospital. The results of this trial will be published in a peer-reviewed journal. TRIAL REGISTRATION NUMBER: jRCTs032210543.
  • 松下 一之, 橋口 照人, 渡邊 広祐, 奥川 喜永, 竹田 真由, 谷本 昭英, 赤羽 俊章, 池尻 誠, 石毛 崇之, 遺伝子・プロテオミクス委員会がんゲノム検査の評価と規制に関する基本的考え方WG2
    医療検査と自動化 49(4) 422-422 2024年8月  
  • 土田 祥央, 村田 正太, 宮部 安規子, 中嶋 優貴, 飯塚 和秀, 佐藤 守, 松下 一之, 中山 智祥, 野村 文夫, 梅村 啓史
    JSBMS Letters 49(Suppl.) 118-118 2024年8月  
  • Kazuki Yoshida, Haruka Sasaki, Hiroyuki Takaoka, Yusei Nishikawa, Shuhei Aoki, Katsuya Suzuki, Satomi Yashima, Noriko Suzuki-Eguchi, Makiko Kinoshita, Tomonori Kanaeda, Keisuke Matsusaka, Hiroki Kohno, Kazuyuki Matsushita, Yoshio Kobayashi
    Circulation reports 6(6) 230-231 2024年6月10日  
  • 松原 未来, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 鈴木 眞, 山下 晃司, 藤川 樹, 村田 正太, 石和田 稔彦, 矢口 貴志, 伊藤 純子, 奥主 朋子, 日野 もえ子, 川崎 健治, 松下 一之
    日本臨床微生物学会雑誌 34(3) 209-213 2024年6月  
  • Shin Suzuki, Yuji Morita, Shota Ishige, Kiyohiro Kai, Kenji Kawasaki, Kazuyuki Matsushita, Kohei Ogura, Tohru Miyoshi-Akiyama, Takeshi Shimizu
    Microbiology (Reading, England) 170(6) 2024年6月  
    Long-term administration of certain macrolides is efficacious in patients with persistent pulmonary Pseudomonas aeruginosa infection, despite how limited the clinically achievable concentrations are, being far below their MICs. An increase in the sub-MIC of macrolide exposure-dependent sensitivity to nitrosative stress is a typical characteristic of P. aeruginosa. However, a few P. aeruginosa clinical isolates do not respond to sub-MIC of macrolide treatment. Therefore, we examined the effects of sub-MIC of erythromycin (EM) on the sensitivity to nitrosative stress together with an efflux pump inhibitor (EPI) phenylalanine arginyl β-naphthylamide (PAβN). The sensitivity to nitrosative stress increased, suggesting that the efflux pump was involved in inhibiting the sub-MIC of macrolide effect. Analysis using efflux pump-mutant P. aeruginosa revealed that MexAB-OprM, MexXY-OprM, and MexCD-OprJ are factors in reducing the sub-MIC of macrolide effect. Since macrolides interfere with quorum sensing (QS), we demonstrated that the QS-interfering agent furanone C-30 (C-30) producing greater sensitivity to nitric oxide (NO) stress than EM. The effect of C-30 was decreased by overproduction of MexAB-OprM. To investigate whether the increase in the QS-interfering agent exposure-dependent sensitivity to nitrosative stress is characteristic of P. aeruginosa clinical isolates, we examined the viability of P. aeruginosa treated with NO. Although treatment with EM could reduce cell viability, a high variability in EM effects was observed. Conversely, C-30 was highly effective at reducing cell viability. Treatment with both C-30 and PAβN was sufficiently effective against the remaining isolates. Therefore, the combination of a QS-interfering agent and an EPI could be effective in treating P. aeruginosa infections.
  • Akiyuki Uzawa, Masahiro Mori, Hiroki Masuda, Mayumi Muto, Ryohei Ohtani, Shinji Aoyama, Kazuyuki Matsushita, Satoshi Kuwabara
    Multiple sclerosis (Houndmills, Basingstoke, England) 13524585241254731-13524585241254731 2024年5月23日  
    BACKGROUND: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a rare neuroinflammatory disorder characterized by acute episodes of central nervous system (CNS) demyelination. Previous studies have reported elevated interleukin (IL)-6 in cerebrospinal fluid (CSF) of MOGAD patients. OBJECTIVE: We examined if CSF IL-6 level increase is associated with clinical parameters in MOGAD. METHODS: IL-6 levels were measured using 44 CSF samples during the acute phase and 6 samples during recovery from 34 MOGAD patients, as well as 65 CSF samples from 45 aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (AQP4Ab + NMOSD), 107 samples from 76 multiple sclerosis patients, and 45 samples from neurodegenerative disease patients. Associations between IL-6 levels and clinical parameters in MOGAD were also evaluated. RESULTS: CSF IL-6 levels were significantly comparably elevated during acute-phase in MOGAD and AQP4Ab + NMOSD, but declined following the acute phase. Among MOGAD patients, CSF IL-6 level was significantly correlated with CSF cell count, greater in patients with brain lesions than spinal cord lesions, and higher in CSF than serum, suggesting that excessive IL-6 is produced predominantly in CNS. Neurological recovery was tended to be poorer in MOGAD patients with higher CSF IL-6 level. CONCLUSION: CSF IL-6 may play important roles in the pathogenesis of MOGAD, especially in CNS inflammation.
  • 鈴木 眞, 宮部 安規子, 斉藤 知子, 瀬川 俊介, 山下 晃司, 菅谷 陸, 川崎 健治, 松下 一之
    日本医学検査学会抄録集 73回 278-278 2024年5月  
  • Hidetoshi Igari, Seiichiro Sakao, Takayuki Ishige, Kengo Saito, Shota Murata, Misuzu Yahaba, Toshibumi Taniguchi, Akiko Suganami, Kazuyuki Matsushita, Yutaka Tamura, Takuji Suzuki, Eiji Ido
    Nature Communications 15(1) 2024年4月29日  
    Abstract Numerous SARS-CoV-2 variant strains with altered characteristics have emerged since the onset of the COVID-19 pandemic. Remdesivir (RDV), a ribonucleotide analogue inhibitor of viral RNA polymerase, has become a valuable therapeutic agent. However, immunosuppressed hosts may respond inadequately to RDV and develop chronic persistent infections. A patient with respiratory failure caused by interstitial pneumonia, who had undergone transplantation of the left lung, developed COVID-19 caused by Omicron BA.5 strain with persistent chronic viral shedding, showing viral fusogenicity. Genome-wide sequencing analyses revealed the occurrence of several viral mutations after RDV treatment, followed by dynamic changes in the viral populations. The C799F mutation in nsp12 was found to play a pivotal role in conferring RDV resistance, preventing RDV-triphosphate from entering the active site of RNA-dependent RNA polymerase. The occurrence of diverse mutations is a characteristic of SARS-CoV-2, which mutates frequently. Herein, we describe the clinical case of an immunosuppressed host in whom inadequate treatment resulted in highly diverse SARS-CoV-2 mutations that threatened the patient’s health due to the development of drug-resistant variants.
  • 庭野 亜美, 佐々木 晴香, 高岡 浩之, 阿部 衣里子, 鎌田 知子, 川崎 健治, 江口 紀子, 小林 欣夫, 松下 一之
    超音波医学 51(Suppl.) S545-S545 2024年4月  
  • 與子田 一輝, 佐々木 晴香, 高岡 浩之, 鎌田 知子, 川崎 健治, 江口 紀子, 小林 欣夫, 松下 一之
    超音波医学 51(Suppl.) S549-S549 2024年4月  
  • Kazuki Yoshida, Haruka Sasaki, Hiroyuki Takaoka, Rei Hashimoto, Kenji Kawasaki, Goro Matsumiya, Kazuyuki Matsushita, Yoshio Kobayashi
    CASE (Philadelphia, Pa.) 8(3Part B) 265-272 2024年3月  
    • Severe progressive PR and TR in adults without histories of cardiac surgery is rare. • Carcinoid heart disease is an important differential in isolated PR and TR. • Three-dimensional TTE is helpful in identifying morphologic abnormalities of the PV. • CCT and cardiovascular magnetic resonance also help evaluate structures near the PV.
  • Takaki Hiwasa, Yoichi Yoshida, Masaaki Kubota, Shu-Yang Li, Bo-Shi Zhang, Tomoo Matsutani, Seiichiro Mine, Toshio Machida, Masaaki Ito, Satoshi Yajima, Mikako Shirouzu, Shigeyuki Yokoyama, Mizuki Sata, Kazumasa Yamagishi, Hiroyasu Iso, Norie Sawada, Shoichiro Tsugane, Minoru Takemoto, Aiko Hayashi, Koutaro Yokote, Yoshio Kobayashi, Kazuyuki Matsushita, Koichiro Tatsumi, Hirotaka Takizawa, Go Tomiyoshi, Hideaki Shimada, Yoshinori Higuchi
    Medicine international 4(5) 45-45 2024年  
    Numerous antibody biomarkers have been reported for cancer and atherosclerosis-related diseases. The major complications of atherosclerosis and diabetes mellitus (DM) are acute ischemic stroke (AIS), cardiovascular disease (CVD) and chronic kidney disease (CKD). Cancer development is accompanied by arterial disorders, such as angiogenesis and atherosclerosis, and DM is a risk factor for the development of certain types of cancer. Atherosclerosis-related diseases and cancers are therefore interrelated and could be detected using a common biomarker. In the present study, the initial screening using the protein array method identified KIAA0513 as an antigen recognized by serum IgG antibodies in patients with atherosclerosis. The amplified luminescent proximity homogeneous assay-linked immunosorbent assay revealed significantly higher serum antibody levels against recombinant KIAA0513 protein in patients with AIS, transient ischemic attack (TIA), DM, CVD, obstructive sleep apnea syndrome (OSAS), CKD and solid cancers, such as esophageal, gastric, colon, lung and breast cancers, compared with healthy donors. A receiver operating characteristic (ROC) analysis revealed that the highest areas under the ROC curves of anti-KIAA0513 antibodies were obtained for esophageal cancer, nephrosclerosis-type CKD and DM. Spearman's correlation analysis revealed that serum anti-KIAA0513 antibody levels were associated with maximum intima-media thickness and plaque score, which are indices of atherosclerosis and stenosis. Serum anti-KIAA0513 antibody markers appear to be useful for diagnosing AIS, TIA, DM, CVD, OSAS, CKD and solid cancers, and may reflect common arterial alterations leading to atherosclerotic and cancerous diseases.
  • Kouichi Kitamura, Tyuji Hoshino, Atsushi Okabe, Masaki Fukuyo, Bahityar Rahmutulla, Nobuko Tanaka, Sohei Kobayashi, Tomoaki Tanaka, Takashi Shida, Mashiro Ueda, Toshinari Minamoto, Hisahiro Matsubara, Atsushi Kaneda, Hideshi Ishii, Kazuyuki Matsushita
    International journal of molecular sciences 24(24) 2023年12月11日  
    The interaction between mRNA and ribosomal RNA (rRNA) transcription in cancer remains unclear. RNAP I and II possess a common N-terminal tail (NTT), RNA polymerase subunit RPB6, which interacts with P62 of transcription factor (TF) IIH, and is a common target for the link between mRNA and rRNA transcription. The mRNAs and rRNAs affected by FUBP1-interacting repressor (FIR) were assessed via RNA sequencing and qRT-PCR analysis. An FIR, a c-myc transcriptional repressor, and its splicing form FIRΔexon2 were examined to interact with P62. Protein interaction was investigated via isothermal titration calorimetry measurements. FIR was found to contain a highly conserved region homologous to RPB6 that interacts with P62. FIRΔexon2 competed with FIR for P62 binding and coactivated transcription of mRNAs and rRNAs. Low-molecular-weight chemical compounds that bind to FIR and FIRΔexon2 were screened for cancer treatment. A low-molecular-weight chemical, BK697, which interacts with FIRΔexon2, inhibited tumor cell growth with rRNA suppression. In this study, a novel coactivation pathway for cancer-related mRNA and rRNA transcription through TFIIH/P62 by FIRΔexon2 was proposed. Direct evidence in X-ray crystallography is required in further studies to show the conformational difference between FIR and FIRΔexon2 that affects the P62-RBP6 interaction.
  • Sohei Kobayashi, Takaki Hiwasa, Kouichi Kitamura, Masayuki Kano, Tyuji Hoshino, Sho Hirano, Mayuko Hashimoto, Masanori Seimiya, Hideaki Shimada, Fumio Nomura, Hisahiro Matsubara, Kazuyuki Matsushita
    Journal of clinical laboratory analysis e24978 2023年11月14日  
    BACKGROUND: At different stages of the disease, biomarkers can help to determine disease progression and recurrence and provide a personalized indicator of therapeutic effectiveness. The serological identification of antigens by recombinant cDNA expression cloning (SEREX) has identified five SEREX antigens. RESULTS: Compared with healthy donors, anti-FIRΔexon2 and anti-SOHLH antibodies (Abs) in the sera of patients with colorectal cancer (CRC) were markedly higher. Furthermore, no correlation was noted between five SEREX antigens and the three tumor markers (CEA, CA19-9, and anti-p53 Abs), indicating that anti-FIRΔexon2 Abs are an independent candidate marker for patients with CRC. Generally, the levels of anti-FIRΔexon2 Abs combined with clinically available tumor markers were determined to be significantly higher compared with CEA, CA19-9. Moreover, in early-stage CRC, the levels of anti-FIRΔexon2 Abs combined with existing tumor markers were higher than those of CEA, CA19-9. CONCLUSION: Due to the highly heterogeneous nature of CRC, a single tumor marker is unlikely to become a standalone diagnostic test due to its commonly insufficient sensitivity and/or specificity. Using a combination antibody detection approach of tumor markers for CRC diagnosis has the potential to be an effective approach. Therefore, the use of serum protein biomarker candidates holds promise for the development of inexpensive, noninvasive, and inexpensive tests for the detection of CRC.
  • Naoki Akizue, Kenichiro Okimoto, Yosuke Hirotsu, Kenji Amemiya, Tatsuya Kaneko, Yuki Ohta, Takashi Taida, Keiko Saito, Tomoaki Matsumura, Motoi Nishimura, Kazuyuki Matsushita, Hitoshi Mochizuki, Tetsuhiro Chiba, Makoto Arai, Jun Kato, Masao Omata, Naoya Kato
    Journal of gastroenterology and hepatology 2023年5月16日  
    BACKGROUND AND AIM: Little is known about genetic mutations in the regenerated mucosa (RM) after endoscopic resection (ER) of esophageal carcinoma. Thus, this study investigates the status of genetic variation in RM after ER of esophageal squamous cell carcinoma (ESCC). METHODS: The study cohort included 19 patients with ESCC. We used an esophageal carcinoma panel to identify target sequences for squamous cell carcinoma (SCC), background mucosa (BM), and RM after ER of ESCC. We used OncoKB to check whether each mutation was a putative driver. RESULTS: We identified 77 mutations of 32 genes in SCC, 133 mutations of 34 genes in BM, and 100 mutations of 29 genes in RM. Putative driver mutations were identified in 20 mutations in 14 cases in SCC, 16 mutations in 10 cases in BM, and 7 mutations in 11 cases in RM. The rate of putative driver mutations to total mutations was significantly lower in RM (26% in SCC vs 12% in BM vs 7% in RM, P = 0.009). Additionally, the rate of cases with TP53 putative driver mutations was significantly lower in RM (63% in SCC vs 37% in BM vs 16% in RM, P = 0.011). The percentage of putative driver mutations and the percentage of cases with a putative driver of TP53 were significantly lower in RM. CONCLUSION: Esophageal RM after ER of ESCC could have a lower risk of carcinogenesis.
  • 松谷 智郎, 廣野 誠一郎, 小林 正芳, 石毛 崇之, 西村 基, 糸賀 栄, 松下 一之, 岩立 康男
    Brain Tumor Pathology 40(Suppl.) 128-128 2023年5月  
  • 清宮 正徳, 米根 鉄矢, 小林 崇平, 浅野 はるな, 川崎 健治, 松下 一之
    電気泳動 67(Suppl.) s42-s42 2023年5月  
  • Takahiro Arasawa, Takaki Hiwasa, Akiko Kagaya, Tetsuro Maruyama, Masaya Uesato, Masayuki Kano, Sohei Kobayashi, Hirotaka Takizawa, Katsuro Iwase, Fumio Nomura, Kazuyuki Matsushita, Hisahiro Matsubara
    BMC cancer 23(1) 356-356 2023年4月18日  
    Colorectal cancer (CRC) is the third most prevalent cancer in the world, yet the sensitivity and specificity of biomarkers for CRC diagnosis are insufficient. In the present study, we performed a protein microarray screening method to identify antibody markers for CRC. Inhibitor of growth family 1 (ING1) was identified as a candidate tumor antigen for CRC using protein microarrays (ProtoArray). Subsequent amplified luminescence proximity homogeneous assay-linked immunosorbent assay using recombinant ING1 protein showed that the serum levels of anti-ING1 antibodies were increased not only in patients with CRC but also in those with esophageal cancer (EC), gastric cancer (GC), breast cancer (BrC), and pancreatic cancer (PC) compared with those of healthy donors (HDs). Antibodies against the ING1 amino acids between 239 and 253 were present at significantly higher levels in patients with CRC than in those with EC, GC, BrC, or PC. Anti-ING1 antibody levels were significantly higher in the patients with CRC at any stages than in the HDs. Immunohistochemical staining revealed higher expression of ING1 protein in CRC cells than in the adjacent normal tissues. In luciferase reporter assays using a CRC cell line, ING1 augmented p53-mediated NOXA promoter activity but attenuated p53-stimulated Bax, p21, and PUMA promoter activities. Consequently, serum anti-ING1 antibodies can be used for sensitive and specific diagnoses of CRC.
  • Motoi Nishimura, Tomoaki Tanaka, Syota Murata, Akiko Miyabe, Takayuki Ishige, Kenji Kawasaki, Masataka Yokoyama, Naoko Hashimoto, Kazuyuki Yamagata, Hidekazu Nagano, Satomi Tojo-Nishimura, Kazuyuki Matsushita
    Scientific reports 13(1) 5731-5731 2023年4月7日  
    Although polymerase chain reaction (PCR) amplification and sequencing of the bacterial 16S rDNA region has numerous scientific applications, it does not provide DNA methylation information. Herein, we propose a simple extension for bisulfite sequencing to investigate 5-methylcytosine residues in the bacterial 16S rDNA region from clinical isolates or flora. Multiple displacement amplification without DNA denaturation was used to preferentially pre-amplify single-stranded bacterial DNA after bisulfite conversion. Following the pre-amplification, the 16S rDNA region was analyzed using nested bisulfite PCR and sequencing, enabling the simultaneous identification of DNA methylation status and sequence data. We used this approach (termed sm16S rDNA PCR/sequencing) to identify novel methylation sites and a methyltransferase (M. MmnI) in Morganella morganii and different methylation motifs among Enterococcus faecalis strains from small volumes of clinical specimens. Further, our analysis suggested that M. MmnI may be correlated to erythromycin resistance. Thus, sm16S rDNA PCR/sequencing is a useful extension method for analyzing the DNA methylation of 16S rDNA regions in a microflora, providing additional information not provided by conventional PCR. Given the relationship between DNA methylation status and drug resistance in bacteria, we believe this technique can be effectively applied in clinical sample testing.
  • 新井 聡子, 楯 真一, 大塚 聡代, 松岡 歩, 錦見 恭子, 高田 章代, 松下 一之, 宇野 隆, 生水 真紀夫, 甲賀 かをり
    超音波医学 50(Suppl.) S557-S557 2023年4月  
  • 與子田 一輝, 佐々木 晴香, 高岡 浩之, 青木 秀平, 鈴木 克也, 八島 聡美, 高橋 愛, 木下 真己子, 江口 紀子, 鎌田 知子, 川崎 健治, 高梨 秀一郎, 松宮 護郎, 小林 欣夫, 松下 一之
    日本循環器学会学術集会抄録集 87回 CO1-1 2023年3月  
  • 與子田 一輝, 佐々木 晴香, 高岡 浩之, 青木 秀平, 鈴木 克也, 八島 聡美, 高橋 愛, 木下 真己子, 江口 紀子, 鎌田 知子, 川崎 健治, 高梨 秀一郎, 松宮 護郎, 小林 欣夫, 松下 一之
    日本循環器学会学術集会抄録集 87回 CO1-1 2023年3月  
  • Sachio Tsuchida, Koji Yamashita, Syota Murata, Akiko Miyabe, Mamoru Satoh, Kazuyuki Matsushita, Tomohiro Nakayama, Fumio Nomura, Hiroshi Umemura
    Journal of Microbiological Methods 207 106706-106706 2023年3月  
    Aspergillus spp. belong to filamentous fungi and sometimes cause invasive aspergillosis which has high mortality. Filamentous fungi are generally identified morphologically. However, morphologic identification is time consuming and requires advanced skills. It is difficult to train technicians and ensure a high level of quality. Therefore, an identification technique that is both accurate and relatively easy to learn is needed. In the present study, we focused on the effects of Yatalase and silica beads, which enable the efficient extraction of proteins via cell wall disruption of Aspergillus spp., and aimed to establish a novel sample preparation method using Yatalase and silica beads to enhance the efficiency of Aspergillus spp. identification with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. The sample preparation method using the combination of Yatalase and silica beads showed higher accuracy for the identification of Aspergillus spp. compared with Yatalase or silica beads alone. The Yatalase/silica beads method also resulted in significantly higher identification scores compared with the conventional method for the identification of Aspergillus fumigatus (n = 33). These findings indicate that our novel Yatalase/silica beads method provides more reliable identification of A. fumigatus than does the conventional method.
  • Kenichiro Okimoto, Yosuke Hirotsu, Makoto Arai, Kenji Amemiya, Naoki Akizue, Yuki Ohta, Takashi Taida, Keiko Saito, Hiroshi Ohyama, Tomoaki Matsumura, Motoi Nishimura, Kazuyuki Matsushita, Keisuke Matsusaka, Toshio Oyama, Hitoshi Mochizuki, Tetsuhiro Chiba, Jun Kato, Jun-Ichiro Ikeda, Osamu Yokosuka, Naoya Kato, Masao Omata
    Cancer medicine 12(7) 8490-8498 2023年2月3日  
    BACKGROUND: This study aimed to investigate the validity of pathological diagnosis of early CRC (E-CRC) from the genetic background by comparing data of E-CRC to colorectal adenoma (CRA) and The Cancer Genome Atlas (TCGA) on advanced CRC (AD-CRC). METHODS: TCGA data on AD-CRC were studied in silico, whereas by next-generation sequencer, DNA target sequences were performed for endoscopically obtained CRA and E-CRC samples. Immunohistochemical staining of mismatch repair genes and methylation of MLH1 was also performed. The presence of oncogenic mutation according to OncoKB for the genes of the Wnt, MAPK, and cell-cycle-signaling pathways was compared among CRA, E-CRC, and AD-CRC. RESULTS: The study included 22 CRA and 30 E-CRC lesions from the Chiba University Hospital and 212 AD-CRC lesions from TCGA data. Regarding the number of lesions with driver mutations in the Wnt and cell-cycle-signaling pathways, E-CRC was comparable to AD-CRC, but was significantly greater than CRA. CRA had significantly more lesions with a driver mutation for the Wnt signaling pathway only, versus E-CRC. CONCLUSIONS: In conclusion, the definition of E-CRC according to the Japanese criteria had a different genetic profile from CRA and was more similar to AD-CRC. Based on the main pathway, it seemed reasonable to classify E-CRC as adenocarcinoma. The pathological diagnosis of E-CRC according to Japanese definition seemed to be valid from a genetic point of view.
  • 清宮 正徳, 鈴木 友乃, 伝福 友加, 米根 鉄矢, 小林 崇平, 松下 一之
    生物試料分析 46(1) 49-49 2023年2月  
  • 清宮 正徳, 安達 愛香, 金子 葵, 北野 萌子, 平井 佑芽, 米根 鉄矢, 小林 崇平, 松下 一之
    生物試料分析 46(1) 50-50 2023年2月  
  • Mizuna Takahashi, Takahiro Tsuchikawa, Takaki Hiwasa, Toru Nakamura, Koji Hontani, Toshihiro Kushibiki, Kazuho Inoko, Hironobu Takano, Yutaka Hatanaka, Kazuyuki Matsushita, Hisahiro Matsubara, Tyuji Hoshino, Masayuki Ohtsuka, Hideaki Shimada, Kimitaka Tanaka, Yoshitsugu Nakanishi, Toshimichi Asano, Takehiro Noji, Keisuke Okamura, Toshiaki Shichinohe, Satoshi Hirano
    Oncology reports 49(2) 2023年2月  
    Biliary cancer has a poor prognosis due to a lack of specific biomarkers and difficulty in diagnosis. The present study aimed to identify serum tumor markers for the diagnosis of biliary cancer via serological identification of antigens by recombinant cDNA expression cloning. Wingless‑type MMTV integration site family, member 7 (WNT7B) was identified as a target antigen, suggesting the presence of serum antibodies against this antigen. Deletion mutants were then prepared to evaluate the response to serum antibodies. When serum antibody levels against WNT7B deletion mutants (WNT7B-92‑2, -92‑260, 2-260 and 184-260) were examined using amplified luminescence proximity homogeneous assay‑linked immunosorbent assay, the levels of the antibody against WNT7B with amino acids 184‑260 were higher in patients with biliary cancer than in healthy donors. Therefore, the region covering residues 184‑260 of WNT7B was decomposed to generate seven peptides, and the levels of antibodies against these peptides were measured. Among them, the levels of antibodies against WNT7B234‑253 and WNT7B244‑260 were higher in patients with biliary cancers than in healthy donors (WNT7B234‑253, P=0.0009; WNT7B244‑260, P=0.0005). The levels of the antibody against the former were specifically high in patients with biliary cancer but not in those with esophageal, gastric, colorectal, pancreatic, or breast cancer. Furthermore, analysis by the cutoff value of WNT7B234‑253 defined by ROC showed a high sensitivity of 70% in patients with biliary cancer. Therefore, the serum levels of the antibody against WNT7B234‑253 may be useful as a marker for biliary cancer diagnosis.
  • 菅谷 陸, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 鈴木 眞, 山下 晃司, 村田 正太, 松下 一之
    千臨技会誌 (142) 35-35 2023年1月  
  • 松田 侑里, 米倉 修二, 須藤 智美, 栗田 惇也, 新井 智之, 飯沼 智久, 鈴木 眞, 山下 晃司, 松下 一之, 髙地 祐輔, 岸本 充, 花澤 豊行
    日本耳鼻咽喉科免疫アレルギー感染症学会誌 3(3) 101-107 2023年  
    非結核性抗酸菌(NTM)によるリンパ節炎の多くは小児例であり,成人では免疫不全例以外での報告は少ない。今回,健康成人に発症したNTMによる耳前部リンパ節炎の1例を経験したので報告する。症例は41歳男性。右耳前部の腫瘤を主訴に近医耳鼻咽喉科を受診し,耳下腺腫瘍が疑われたため当科へ紹介となった。初診時,右耳前部皮下に20 mm大の可動性不良な硬結を触れ,超音波検査では右耳下腺上極の被膜付近から皮下組織へ広がる境界不明瞭・辺縁不整な腫瘤を認めた。MRI検査では被膜部分は造影されるが,内部は造影効果の少ない腫瘤性病変として描出された。穿刺吸引細胞診では悪性所見は認めず,炎症を伴う肉芽病変が示唆された。穿刺物の抗酸菌培養およびPCRは陰性であった。精査中に膿瘍形成後に自壊したため,膿汁を培養検査に提出したところ,質量分析法および遺伝子解析から起因菌は迅速発育抗酸菌であるMycobacterium mageritenseと同定された。感染症内科にコンサルトの上,sulfamethoxazole/trimethoprim合剤とlevofloxacinによる薬物療法を開始したが,2ヵ月間の抗菌薬投与でも改善が乏しかったため,局所麻酔下で外科的切除を行った。病理所見では乾酪壊死を伴う類上皮細胞肉芽腫を認め,NTMによるリンパ節炎として矛盾しない結果であった。迅速発育抗酸菌の治療方針は確立されておらず,患者の背景因子,病変の状態,および薬剤感受性などを考慮して,個々の症例に対応した治療を展開する必要がある。
  • Hideki Ogura, Jin Gohda, Xiuyuan Lu, Mizuki Yamamoto, Yoshio Takesue, Aoi Son, Sadayuki Doi, Kazuyuki Matsushita, Fumitaka Isobe, Yoshihiro Fukuda, Tai-Ping Huang, Takamasa Ueno, Naomi Mambo, Hiromoto Murakami, Yasushi Kawaguchi, Jun-Ichiro Inoue, Kunihiro Shirai, Sho Yamasaki, Jun-Ichi Hirata, Satoshi Ishido
    Nature communications 13(1) 7063-7063 2022年12月16日  
    Although the importance of virus-specific cytotoxic T lymphocytes (CTL) in virus clearance is evident in COVID-19, the characteristics of virus-specific CTLs related to disease severity have not been fully explored. Here we show that the phenotype of virus-specific CTLs against immunoprevalent epitopes in COVID-19 convalescents might differ according to the course of the disease. We establish a cellular screening method that uses artificial antigen presenting cells, expressing HLA-A*24:02, the costimulatory molecule 4-1BBL, SARS-CoV-2 structural proteins S, M, and N and non-structural proteins ORF3a and nsp6/ORF1a. The screen implicates SARS-CoV-2 M protein as a frequent target of IFNγ secreting CD8+ T cells, and identifies M198-206 as an immunoprevalent epitope in our cohort of HLA-A*24:02 positive convalescent COVID-19 patients recovering from mild, moderate and severe disease. Further exploration of M198-206-specific CD8+ T cells with single cell RNA sequencing reveals public TCRs in virus-specific CD8+ T cells, and shows an exhausted phenotype with less differentiated status in cells from the severe group compared to cells from the moderate group. In summary, this study describes a method to identify T cell epitopes, indicate that dysfunction of virus-specific CTLs might be an important determinant of clinical outcomes.
  • 山下 晃司, 伴 さやか, 新居 鉄平, 宮部 安規子, 村田 正太, 川崎 健治, 松下 一之, 渡辺 哲, 矢口 貴志
    日本臨床微生物学会雑誌 33(Suppl.1) 294-294 2022年12月  
  • 西村 基, 宮部 安規子, 村田 正太, 石毛 崇之, 川崎 健治, 松下 一之
    日本臨床微生物学会雑誌 33(Suppl.1) 273-273 2022年12月  
  • 松原 未来, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 鈴木 眞, 山下 晃司, 藤川 樹, 村田 正太, 石和田 稔彦, 矢口 貴志, 伊藤 純子, 奥主 朋子, 日野 もえ子, 川崎 健治, 松下 一之
    日本臨床微生物学会雑誌 33(Suppl.1) 232-232 2022年12月  
  • Ami Niwano, Haruka Sasaki, Hiroyuki Takaoka, Kenji Kawasaki, Kentaro Atarashi, Jun-Ichiro Ikeda, Goro Matsumiya, Kazuyuki Matsushita, Yoshio Kobayashi
    Journal of cardiology cases 26(6) 404-406 2022年12月  
    UNLABELLED: Papillary fibroelastoma (PFE) is a rare, slow-growing cardiac tumor. We encountered an 80-year-old man with PFE accidentally revealed by transthoracic echocardiography (TTE) to evaluate cardiac function before a non-cardiac operation. A 10-mm mass lesion adhered to the anterior papillary muscle of the left ventricle, which had not been detected with TTE performed nine months before. Emergency cardiac surgery to remove the mass was performed, and the mass was diagnosed as a PFE. The PFE grew to 10 mm in a maximum of 9 months; to our knowledge, this is the fastest growth of PFE in the left ventricle reported to date. LEARNING OBJECTIVE: Papillary fibroelastoma (PFE) is a rare, slow-growing cardiac tumor. The surgical indication of PFE is sometimes controversial. The rapid growth of PFE might be considered as a criterion for surgery because this might result in the rapid progression of symptoms and complications.
  • 松原 未来, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 鈴木 眞, 山下 晃司, 藤川 樹, 村田 正太, 石和田 稔彦, 矢口 貴志, 伊藤 純子, 奥主 朋子, 日野 もえ子, 川崎 健治, 松下 一之
    日本臨床微生物学会雑誌 33(Suppl.1) 232-232 2022年12月  
  • 鈴木 眞, 宮部 安規子, 齊藤 知子, 瀬川 俊介, 堀田 恵海, 山下 晃司, 松原 未来, 菅谷 陸, 藤川 樹, 村田 正太, 大楠 美佐子, 石和田 稔彦, 川崎 健治, 松下 一之
    日本臨床微生物学会雑誌 33(Suppl.1) 287-287 2022年12月  
  • 山下 晃司, 伴 さやか, 新居 鉄平, 宮部 安規子, 村田 正太, 川崎 健治, 松下 一之, 渡辺 哲, 矢口 貴志
    日本臨床微生物学会雑誌 33(Suppl.1) 294-294 2022年12月  
  • Yoichi Mashimo, Keiko Yamazaki, Takahiro Kageyama, Shigeru Tanaka, Toshibumi Taniguchi, Kazuyuki Matsushita, Hidetoshi Igari, Hideki Hanaoka, Koutaro Yokote, Hiroshi Nakajima, Yoshihiro Onouchi
    Journal of Infection 85(6) 702-769 2022年11月  
  • 澤井 摂, 石毛 崇之, 宇津野 恵美, 関根 瑞香, 杉山 淳比古, 尾内 善広, 榊原 隆次, 松下 一之, 市川 智彦, 桑原 聡
    臨床神経学 62(Suppl.) S287-S287 2022年10月  
  • Yuri Imaizumi, Takayuki Ishige, Tatsuki Fujikawa, Akiko Miyabe, Shota Murata, Kenji Kawasaki, Motoi Nishimura, Toshibumi Taniguchi, Hidetoshi Igari, Kazuyuki Matsushita
    Clinica chimica acta; international journal of clinical chemistry 536 6-11 2022年9月14日  
    BACKGROUND: Tracking SARS-CoV-2 variants of concern (VOC) by genomic sequencing is time-consuming. The rapid screening of VOCs is necessary for clinical laboratories. In this study, we developed a rapid screening method based on multiplex RT-PCR by extended S-gene target failure (eSGTF), a false negative result caused by S-gene mutations. METHODS: Three S-gene target (SGT) regions (SGT1, codons 65-72; SGT2, codons 152-159; and SGT3, codons 370-377) and an N-gene region (for internal control) were detected in single-tube. Four types of VOC (Alpha, Delta, Omicron BA.1, and Omicron BA.2) are classified by positive/negative patterns of 3 S-gene regions (eSGTF pattern). RESULTS: The eSGTF patterns of VOCs were as follows (SGT1, SGT2, SGT3; P, positive; N, negative): Alpha, NPP; Delta, PNP; Omicron BA.1, NPN pattern; and Omicron BA.2, PPN. As compared with the S-gene sequencing, eSGTF patterns were identical to the specific VOCs (concordance rate = 96.7%, N = 206/213). Seven samples with discordant results had a minor mutation in the probe binding region. The epidemics of VOCs estimated by eSGTF patterns were similar to those in Japan. CONCLUSIONS: Multiplex RT-PCR and eSGTF patterns enable high-throughput screening of VOCs. It will be useful for the rapid determination of VOCs in clinical laboratories.
  • Hidetoshi Igari, Haruna Asano, Shota Murata, Toshihiko Yoshida, Kenji Kawasaki, Takahiro Kageyama, Key Ikeda, Hiromi Koshikawa, Yoshio Okuda, Misao Urushihara, Hitoshi Chiba, Misuzu Yahaba, Toshibumi Taniguchi, Kazuyuki Matsushita, Ichiro Yoshino, Koutaro Yokote, Hiroshi Nakajima
    Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 28(11) 1483-1488 2022年7月20日  
    INTRODUCTION: Vaccine effectiveness against SARS-CoV-2 infections decreases due to waning immunity, and booster vaccination was therefore introduced. We estimated the anti-spike antibody (AS-ab) recovery by booster vaccination and analyzed the risk factors for SARS-CoV-2 infections. METHODS: The subjects were health care workers (HCWs) in a Chiba University Hospital vaccination cohort. They had received two doses of vaccine (BNT162b2) and a booster vaccine (BNT162b2). We retrospectively analyzed AS-ab titers and watched out for SARS-CoV-2 infection for 90 days following booster vaccination. RESULTS: AS-ab titer eight months after two-dose vaccinations had decreased to as low as 587 U/mL (median, IQR (interquartile range) 360-896). AS-ab titer had then increased to 22471 U/mL (15761-32622) three weeks after booster vaccination. There were no significant differences among age groups. A total of 1708 HCWs were analyzed for SARS-CoV-2 infection, and 48 of them proved positive. SARS-CoV-2 infections in the booster-vaccinated and non-booster groups were 1.8% and 4.0%, respectively, and were not significant. However, when restricted to those 20-29 years old, SARS-CoV-2 infections in the booster-vaccinated and non-booster groups were 2.9% and 13.6%, respectively (p = 0.04). After multivariate logistic regression, COVID-19 wards (adjusted odds ratio (aOR):2.9, 95% confidence interval (CI) 1.5-5.6) and those aged 20-49 years (aOR:9.7, 95%CI 1.3-71.2) were risk factors for SARS-CoV-2 infection. CONCLUSIONS: Booster vaccination induced the recovery of AS-ab titers. Risk factors for SARS-CoV-2 infection were HCWs of COVID-19 wards and those aged 20-49 years. Increased vaccination coverage, together with implementing infection control, remains the primary means of preventing HCWs from SARS-CoV-2 infection.
  • Kuno Suzuki, Hideyoshi Igata, Motoki Abe, Yusuke Yamamoto, Terunao Iwanaga, Hiroaki Kanzaki, Naoya Kato, Nobuko Tanaka, Kenji Kawasaki, Kazuyuki Matsushita, Ryu Samashima, Keiji Tsukino, Akira Yokomizo, Yosuke Miyashita, Issei Sumiyoshi, Kazuhisa Takahashi, Nobuko Serizawa, Ko Tomishima, Akihito Nagahara, Yumiko Ishizuka, Yoshiya Horimoto, Masayoshi Nagata, Keisuke Ishikawa, Shigeo Horie, Shuichiro Shiina, Motomi Nasu, Takashi Hashimoto, Shinji Mine, Shingo Kawano, Kiichi Sugimoto, Kazuhiro Sakamoto, Hiroyuki Takemura, Mitsuru Wakita, Yoko Tabe, Shunsuke Kato, Yohei Miyagi, Hiroyuki Adachi, Tetsuya Isaka, Hiroyuki Ito, Takashi Yamanaka, Tatsuya Yoshida, Toshinari Yamashita, Takashi Ogata, Takanobu Yamada, Takashi Oshima, Naoto Yamamoto, Masaaki Murakawa, Soichiro Morinaga, Satoshi Kobayashi, Shun Tezuka, Makoto Ueno, Mitsuyuki Koizumi, Kimito Osaka, Takeshi Kishida, Sumito Sato, Yo Mikayama, Manabu Shiozawa, Yasuhiro Inokuchi, Mitsuhiro Furuta, Nozomu Machida, Shinya Sato, Yoshihiko Yano, Atsushi Miwa, Kazuto Ito, Isao Kurosawa, Osamu Kikuchi, Hiromitsu Tazawa, Manabu Muto, Takashi Honda, Hiroki Kawashima, Masatoshi Ishigami, Yutaka Saito, Hiroyuki Daiko, Takaki Yoshikawa, Yukihide Kanemitsu, Ken Kato, Minoru Esaki, Takuji Okusaka, Hiromi Sakamoto, Teruhiko Yoshida, Takahiro Ochiya, Mitsuhito Sasaki, Masafumi Ikeda, Masashi Kudo, Naoto Gotohda, Shuichi Mitsunaga, Takeshi Kuwata, Takashi Kojima, Tatsuro Murano, Tomonori Yano, Taiki Yamaji, Takahisa Matsuda, Shoichiro Tsugane, Kazuki Hashimoto, Kazuhiko Yamada, Nobuyuki Takemura, Kyoji Ito, Fuminori Mihara, Akihiko Shimomura, Kunitoshi Shigeyasu, Kazuhiro Noma, Toshiyoshi Fujiwara, Hideki Yamamoto, Mizuki Morita, Shinichi Toyooka, Akihiro Tamori, Tasuku Nakabori, Kenji Ikezawa, Kazuyoshi Ohkawa, Kei Kunimasa, Kazumi Nishino, Toru Kumagai, Toshihiro Kudo, Naotoshi Sugimoto, Masayoshi Yasui, Takeshi Omori, Hiroshi Miyata, Toru Kimura, Tomohiro Maniwa, Jiro Okami, Hiroki Kusama, Nobuyoshi Kittaka, Takahiro Nakayama, Masashi Nakayama, Yasutomo Nakai, Kazuo Nishimura, Shoji Yotsui, Takashi Yamamoto, Tomoyuki Yamasaki, Emi Yamashita, Kazune Saito, Keiichi Yoshida, Masayuki Ohue, Masakazu Koda, Tatsuya Yamaguchi, Masami Tanaka, Takashi Nishizawa, Tetsuhiko Taira, Junko Kawano, Yasuaki Sagara, Yosuke Horita, Yoshiaki Mihara, Tetsuya Hamaguchi, Okihide Suzuki, Yoichi Kumagai, Hideyuki Ishida, Motoki Yamagishi, Hideaki Shimoyama, Haruaki Sasaki, Takehiko Nakasato, Takeshi Shichijo, Takashi Fukagai, Kota Nishimura, Kidai Hirayama, Masashi Morita, Yujin Kudo, Susumu Takeuchi, Norihiko Ikeda, Naohiro Kamoda, Kazunori Namiki, Yoshio Ohno, Tomohiro Umezu, Yoshiki Murakami, Masahiko Kuroda
    Cancer Science 113(6) 2144-2166 2022年6月  
    Liquid biopsy is expected to be a promising cancer screening method because of its low invasiveness and the possibility of detecting multiple types in a single test. In the last decade, many studies on cancer detection using small RNAs in blood have been reported. To put small RNA tests into practical use as a multiple cancer type screening test, it is necessary to develop a method that can be applied to multiple facilities. We collected samples of eight cancer types and healthy controls from 20 facilities to evaluate the performance of cancer type classification. A total of 2,475 cancer samples and 496 healthy control samples were collected using a standardized protocol. After obtaining a small RNA expression profile, we constructed a classification model and evaluated its performance. First, we investigated the classification performance using samples from five single facilities. Each model showed areas under the receiver curve (AUC) ranging from 0.67 to 0.89. Second, we performed principal component analysis (PCA) to examine the characteristics of the facilities. The degree of hemolysis and the data acquisition period affected the expression profiles. Finally, we constructed the classification model by reducing the influence of these factors, and its performance had an AUC of 0.76. The results reveal that small RNA can be used for the classification of cancer types in samples from a single facility. However, interfacility biases will affect the classification of samples from multiple facilities. These findings will provide important insights to improve the performance of multiple cancer type classifications using small RNA expression profiles acquired from multiple facilities.
  • 栃木 透, 松下 一之, 丸山 哲郎, 遠藤 悟史, 今西 俊介, 大平 学, 丸山 通広, 松原 久裕
    日本内分泌外科学会雑誌 39(Suppl.1) S180-S180 2022年6月  

MISC

 1315

書籍等出版物

 2

講演・口頭発表等

 119

担当経験のある科目(授業)

 9

共同研究・競争的資金等の研究課題

 41

産業財産権

 25

その他

 1
  • 千葉県 精度管理委員 千葉市 精度管理委員 船橋市 精度管理委員