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CYR61 confers chemoresistance by upregulating survivin expression in triple-negative breast cancer
被引:2
|作者:
Kim, Hyungjoo
[1
]
Son, Seogho
[1
]
Ko, Yunhyo
[1
]
Lim, Hogeun
[1
]
Lee, Joohyung
[1
]
Lee, Kyung-Min
[1
,2
,3
]
Shin, Incheol
[1
,2
,3
]
机构:
[1] Hanyang Univ, Dept Life Sci, Seoul 04763, South Korea
[2] Hanyang Univ, Nat Sci Inst, Seoul 04763, South Korea
[3] 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:
DRUG-RESISTANCE;
CELL-SURVIVAL;
STEM-CELLS;
GROWTH;
METASTASIS;
INHIBITION;
ACTIVATION;
TRANSITION;
PATHWAY;
GENES;
D O I:
10.1093/carcin/bgae013
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Cysteine-rich angiogenic inducer 61 (CYR61) is a protein from the CCN family of matricellular proteins that play diverse regulatory roles in the extracellular matrix. CYR61 is involved in cell adhesion, migration, proliferation, differentiation, apoptosis, and senescence. Here, we show that CYR61 induces chemoresistance in triple-negative breast cancer (TNBC). We observed that CYR61 is overexpressed in TNBC patients, and CYR61 expression correlates negatively with the survival of patients who receive chemotherapy. CYR61 knockdown reduced cell migration, sphere formation and the cancer stem cell (CSC) population and increased the chemosensitivity of TNBC cells. Mechanistically, CYR61 activated Wnt/beta-catenin signaling and increased survivin expression, which are associated with chemoresistance, the epithelial-mesenchymal transition, and CSC-like phenotypes. Altogether, our study demonstrates a novel function of CYR61 in chemotherapy resistance in breast cancer. Our results demonstrated that CYR61 is overexpressed in TNBC and that CYR61 upregulates survivin expression through activation of Wnt/beta-catenin signaling, leading to an aggressive phenotype of TNBC including chemoresistance. Graphical Abstract
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页码:510 / 519
页数:10
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