ID | 62858 |
フルテキストURL | |
著者 |
Taniguchi, Fumitaka
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
Nyuya, Akihiro
Department of Clinical Oncology, Kawasaki Medical School
Toshima, Toshiaki
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
Yasui, Kazuya
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
Mori, Yoshiko
Department of Clinical Genetics & Digestive Tract & General Surgery, Saitama Medical Center, Saitama Medical University,
Okawaki, Makoto
Department of Clinical Oncology, Kawasaki Medical School
Kishimoto, Hiroyuki
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
Kaken ID
Umeda, Yuzo
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
Kaken ID
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Fujiwara, Toshiyoshi
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
ORCID
Kaken ID
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Tanioka, Hiroaki
Department of Clinical Oncology, Kawasaki Medical School
Yamaguchi, Yoshiyuki
Department of Clinical Oncology, Kawasaki Medical School
Goel, Ajay
Department of Molecular Diagnostics & Experimental Therapeutics, Beckman Research Institute of City of Hope Comprehensive Cancer Center
Nagasaka, Takeshi
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry & Pharmaceutical Sciences
ORCID
Kaken ID
publons
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抄録 | Aim: To evaluate whether PCR-reverse sequence-specific oligonucleotide can examine the concordance between liquid biopsy and metastatic lesions with acquired resistance. Materials & methods: We examined acquired mutations in chemoresistant lesions and blood obtained from four patients with RAS wildtype metastatic colorectal cancer who underwent treatment with anti-epidermal growth factor receptor antibodies. Results: In one patient, metastatic lesions harbored diverse acquired mutations in KRAS in all seven metastases; the two acquired mutations were detectable in blood collected after the patient acquired resistance. None of the other patients exhibited liquid biopsy mutations, except one, with a BRAF mutation confirmed in primary tumor and peritoneal dissemination. Conclusion: Liquid biopsy based on PCR-reverse sequence-specific oligonucleotide is a successful procedure for capturing acquired mutations with precise information on the RAS mutational spectrum.
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キーワード | Acquired mutations
BRAF
colorectal cancer
liquid biopsy
PCR-rSSO
RAS
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出版物タイトル |
Future Science OA
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出版者 | Future Science Ltd.
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開始ページ | FSO757
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ISSN | 2056-5623
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資料タイプ |
学術雑誌論文
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言語 |
英語
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OAI-PMH Set |
岡山大学
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著作権者 | © 2021 Authors
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論文のバージョン | publisher
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DOI | |
Web of Science KeyUT | |
関連URL | isVersionOf https://doi.org/10.2144/fsoa-2021-0059
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