このエントリーをはてなブックマークに追加


ID 63894
JaLCDOI
フルテキストURL
76_4_399.pdf 2.32 MB
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
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.
キーワード
breast cancer
short-term hormone therapy
gene expression profiling
Ki-67
targeted therapy
Amo Type
Original Article
出版物タイトル
Acta Medica Okayama
発行日
2022-08
76巻
4号
出版者
Okayama University Medical School
開始ページ
399
終了ページ
408
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
英語
著作権者
Copyright Ⓒ 2022 by Okayama University Medical School
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT