Upregulation of PAG1/Cbp contributes to adipose-derived mesenchymal stem cells promoted tumor progression and chemoresistance in breast cancer

被引:25
作者
Lu, Yunshu [1 ,2 ]
Yang, Yipeng [1 ,2 ]
Liu, Yan [3 ]
Hao, Yajuan [1 ,2 ]
Zhang, Yijian [1 ,2 ]
Hu, Yunpint [1 ,2 ]
Jiang, Lin [1 ,2 ]
Gong, Yurong [1 ,2 ]
Wu, Kejin [4 ]
Liu, Yingbin [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Lab Gen Surg, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Gen Surg, Xinhua Hosp, Sch Med, Shanghai 200092, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Dept Pharm, Xinhua Hosp, Shanghai 200092, Peoples R China
[4] Fudan Univ, Breast Surg Obstet & Gynaecol Hosp, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
ASCs; Breast cancer; PAG1/Cbp; Chemoresistance; Src; STROMAL CELLS; MULTIDRUG-RESISTANCE; CARCINOMA-CELLS; SRC INHIBITION; IN-VITRO; C-SRC; TISSUE; PROLIFERATION; INVASION; ACTIVATION;
D O I
10.1016/j.bbrc.2017.10.118
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
C-terminal Src kinase (Csk)-binding protein (Cbp) is a ubiquitously expressed transmembrane adaptor protein which regulating Src family kinase (SFK) activities. Although SFKs are well known for their involvement in breast cancer, the function of Cbp in breast carcinogenesis upon the adipose-tumor microenvironment has not been investigated. Here, we reported that adipose-derived mesenchymal stem cells (ASCs) induced increased expression of Cbp accompanied by enhanced cell proliferation and chemotherapy resistance in breast cancer cell MCF-7/ADR. Depletion of Cbp in breast cancer cell by RNA interference led to remarkable inhibition of cell proliferation, invasion as well as synergy with adriamycin hydrochloride to suppress the tumor growth. Furthermore, silencing of Cbp concomitantly inhibited the expression of phosphoryl of Src, AKT and mTOR signals. Our study highlights the underlying mechanism of cross interaction between ASCs and breast cancer cells, and indicates that PAG1/Cbp in breast cancer cell may modulate tumor progression and acquired chemoresistance in the ASCs-associated breast cancer microenvironment through Src and AKT/mTOR pathways. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:719 / 727
页数:9
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