题名 | Subtyping of triple-negative breast cancers: its prognostication and implications in diagnosis of breast origin |
作者 | |
通讯作者 | Tse, G. M. |
发表日期 | 2024-04-01
|
DOI | |
发表期刊 | |
EISSN | 2059-7029
|
卷号 | 9期号:4 |
摘要 | Background: Triple-negative breast cancer (TNBC) subtyping by gene profiling has provided valuable clinical information. Here, we aimed to evaluate the relevance of TNBC subtyping using immunohistochemistry (IHC), which could be a more clinically practical approach, for prognostication and applications in patient management. Methods: A total of 123 TNBC cases were classified using androgen receptor (AR), CD8, Forkhead box C1 protein (FOXC1), and doublecortin-like kinase 1 (DCLK1) into luminal androgen receptor (LAR), basal-like immunosuppressive (BLIS), mesenchymal-like (MES), and immunomodulatory (IM) subtypes. The IM cases were further divided into the IM-excluded and IM-inflamed categories by CD8 spatial distribution. Their clinicopathological and biomarker profiles and prognoses were evaluated. Results: LAR (28.6%) and MES (11.2%) were the most and least frequent subtypes. The IHC-TNBC subtypes demonstrated distinct clinicopathological features and biomarker profiles, corresponding to the reported features in gene profiling studies. IM-inflamed subtype had the best outcome, while BLIS had a significantly poorer survival. Differential breast-specific marker expressions were found. Trichorhinophalangeal syndrome type 1 (TRPS1) was more sensitive for IM-inflamed and BLIS, GATA-binding protein 3 (GATA3) for IM-excluded and MES, and gross cystic disease fluid protein 15 (GCDFP15) for LAR subtypes. Conclusions: Our findings demonstrated the feasibility of IHC surrogates to stratify TNBC subtypes with distinct features and prognoses. The IM subtype can be refined by its CD8 spatial pattern. Breast-specific marker expression varied among the subtypes. Marker selection should be tailored accordingly. |
关键词 | |
相关链接 | [来源记录] |
收录类别 | |
语种 | 英语
|
学校署名 | 其他
|
资助项目 | Health and medical research fund[08190586]
; CUHK direct grant[2020.004]
; Shenzhen Key Medical Discipline Construction Fund[SZXK015]
|
WOS研究方向 | Oncology
|
WOS类目 | Oncology
|
WOS记录号 | WOS:001234882200001
|
出版者 | |
来源库 | Web of Science
|
引用统计 |
被引频次[WOS]:2
|
成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/788327 |
专题 | 南方科技大学第一附属医院 |
作者单位 | 1.Jinan Univ, Shenzhen Peoples Hosp,Clin Med Coll 2, Div Breast Surg, Dept Gen Surg, Shenzhen, Peoples R China 2.Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen, Peoples R China 3.Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anat & Cellular Pathol, State Key Lab Translat Oncol, Hong Kong, Peoples R China 4.Kwong Wah Hosp, Dept Pathol, Hong Kong, Peoples R China 5.Tuen Mun Hosp, Dept Pathol, Hong Kong, Peoples R China 6.Prince Wales Hosp, Dept Anat & Cellular Pathol, Shatin, Ngan Shing St, Hong Kong, Peoples R China |
第一作者单位 | 南方科技大学第一附属医院 |
推荐引用方式 GB/T 7714 |
Hu, H.,Tong, K.,Tsang, J. Y.,et al. Subtyping of triple-negative breast cancers: its prognostication and implications in diagnosis of breast origin[J]. ESMO OPEN,2024,9(4).
|
APA |
Hu, H..,Tong, K..,Tsang, J. Y..,Ko, C. W..,Tam, F..,...&Tse, G. M..(2024).Subtyping of triple-negative breast cancers: its prognostication and implications in diagnosis of breast origin.ESMO OPEN,9(4).
|
MLA |
Hu, H.,et al."Subtyping of triple-negative breast cancers: its prognostication and implications in diagnosis of breast origin".ESMO OPEN 9.4(2024).
|
条目包含的文件 | 条目无相关文件。 |
|
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论