ID | 63894 |
JaLCDOI | |
フルテキストURL | |
著者 |
Kajiwara, Yukiko
Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Iwamoto, Takayuki
Departments of Breast and Endocrine Surgery, Okayama University Hospital
Zhu, Yidan
Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kochi, Mariko
Departments of Breast and Endocrine Surgery, Okayama University Hospital
Shien, Tadahiko
Departments of Breast and Endocrine Surgery, Okayama University Hospital
Taira, Naruto
Departments of Breast and Endocrine Surgery, Okayama University Hospital
Doihara, Hiroyoshi
Departments of Breast and Endocrine Surgery, Okayama University Hospital
Toyooka, Shinichi
Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
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抄録 | According to a recent report, a low Ki67 level after short-term preoperative hormone therapy (post-Ki67) might suggest a more favorable prognosis compared with a high post-Ki67 level in patients with hormone receptorpositive/human epidermal growth factor 2-negative (HR+/HER2−) breast cancer with high levels of Ki67. This study aimed to evaluate the pre-treatment genetic differences between these two patient groups. Forty-five luminal B-like patients were stratified into two groups, namely, a group with high (H→H) and one with low (H→L) Ki67 levels after short-term preoperative aromatase inhibitor (AI) treatment. We compared pre-treatmentgene expression profiles between the two groups. In gene level analysis, there was no significant difference between the two groups by the class comparison test. In pathway analysis, five metabolism-related gene sets were significantly upregulated in the H→L group (p≤0.05). In the search for novel targets, five genes (PARP, BRCA2, FLT4, CDK6, and PDCD1LG2) showed significantly higher expression in the H→H group (p≤0.05). Several metabolism-related pathways were associated with sensitivity to AI. In the future, it will be necessary to seek out new therapeutic strategies for the poor prognostic group with high post-Ki67.
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キーワード | breast cancer
short-term hormone therapy
gene expression profiling
Ki-67
targeted therapy
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Amo Type | Original Article
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出版物タイトル |
Acta Medica Okayama
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発行日 | 2022-08
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巻 | 76巻
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号 | 4号
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出版者 | Okayama University Medical School
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開始ページ | 399
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終了ページ | 408
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ISSN | 0386-300X
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NCID | AA00508441
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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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著作権者 | Copyright Ⓒ 2022 by Okayama University Medical School
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論文のバージョン | publisher
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査読 |
有り
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PubMed ID | |
Web of Science KeyUT |