Immune Checkpoint Blockades in Triple-Negative Breast Cancer: Current State and Molecular Mechanisms of Resistance

被引:16
|
作者
Kim, Hyungjoo [1 ,2 ]
Choi, Je-Min [1 ,3 ,4 ,5 ]
Lee, Kyung-min [1 ,3 ,4 ,5 ]
机构
[1] Hanyang Univ, Coll Nat Sci, Dept Life Sci, Seoul 04763, South Korea
[2] Penta Medix Co Ltd, Seongnam Si 13449, South Korea
[3] Hanyang Univ, Res Inst Nat Sci, Seoul 04763, South Korea
[4] Hanyang Univ, Res Inst Convergence Basic Sci, Seoul 04763, South Korea
[5] Hanyang Univ, Hanyang Inst Biosci & Biotechnol, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
immune checkpoint blockade; TNBC; resistance; IMMUNOHISTOCHEMISTRY IHC ASSAYS; PEMBROLIZUMAB PLUS CHEMOTHERAPY; TUMOR-INFILTRATING LYMPHOCYTES; T-CELL IMMUNOTHERAPY; INDOLEAMINE 2,3-DIOXYGENASE; DOUBLE-BLIND; OPEN-LABEL; PD-L1; EXPRESSION; CRYOABLATION;
D O I
10.3390/biomedicines10051130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immune checkpoint blockades (ICBs) have revolutionized cancer treatment. Recent studies have revealed a subset of triple-negative breast cancer (TNBC) to be considered as an immunogenic breast cancer subtype. Characteristics of TNBC, such as higher mutation rates and number of tumor-infiltrating immune cells, render the immunogenic phenotypes. Consequently, TNBCs have shown durable responses to ICBs such as atezolizumab and pembrolizumab in clinic. However, a significant number of TNBC patients do not benefit from these therapies, and mechanisms of resistance are poorly understood. Here, we review biomarkers that predict the responsiveness of TNBCs to ICB and recent advances in delineating molecular mechanisms of resistance to ICBs.
引用
收藏
页数:17
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