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利用炎症特征:炎性乳腺癌生物标志物综述

英文原题:Harnessing the inflammatory signature: a review for biomarkers in inflammatory breast cancer.

查看英文原题

Harnessing the inflammatory signature: a review for biomarkers in inflammatory breast cancer.

PubMed 2025/12/01(内容时间) QJM Q1 · IF 8.9(JCR 2025)

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中文摘要

炎性乳腺癌(IBC)是一种高度侵袭性的乳腺癌亚型,以快速进展和较差的生存结局为特征。近年来,关于IBC临床和分子特征的研究为其诊断和治疗带来了新的希望。然而,IBC的预后仍然极差,迫切需要新的生物标志物来识别IBC患者的个体特征。本综述讨论了IBC生物标志物的最新研究,尤其是与独特临床IBC特征相关的生物标志物,包括肿瘤栓子相关标志物和肿瘤微环境(TME)相关标志物。基于TME中免疫细胞的生物标志物,如肿瘤相关巨噬细胞(TAMs)、TIL(肿瘤浸润淋巴细胞)(TILs)、肥大细胞、细胞因子和趋化因子(如CCL2),可能参与IBC的发生、进展和治疗耐药。本研究还确定了IBC的有效生物标志物,并强调了与独特临床IBC特征相关的生物标志物,这些标志物可能为IBC的诊断、预后和治疗提供有力证据。

展开英文摘要原文

Inflammatory breast cancer (IBC) is a highly aggressive breast cancer subtype characterized by rapid progression and poor survival outcomes. In recent years, research on the clinical and molecular features of IBC has brought new hope for its diagnosis and treatment.

However, the prognosis of IBC remains extremely poor and novel biomarkers to identify the individual characteristics of patients with IBC are warranted. This review discussed the latest research on IBC biomarkers, especially the unique clinical IBC characterization-related biomarkers, including tumor emboli-related markers and tumor microenvironment (TME)-related markers.

Biomarkers based on immune cells in the TME, such as tumor-associated macrophages (TAMs), tumor-infiltrating lymphocytes (TILs), mast cells, cytokines, and chemokines (e. g. CCL2), may be involved in the development, progression, and treatment resistance of IBC.

This study also identified effective biomarkers for IBC and emphasized unique clinical IBC characterization-related biomarkers that may provide strong evidence in IBC diagnosis, prognosis, and therapeutics.

论文信息

作者
Hu Y、Li J、Wang X、Ji H、Niu X
单位
Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin, Heilongjiang, China.China
文献类型
综述
期刊
QJM : monthly journal of the Association of Physicians2025 Dec 1
原文标识
PubMed 40990804 · DOI 10.1093/qjmed/hcaf219