BAG3-positive pancreatic stellate cells promote migration and invasion of pancreatic ductal adenocarcinoma

被引:16
作者
Yuan, Ye [1 ,2 ,3 ,4 ,5 ]
Jiang, Jing-Yi [1 ,2 ,3 ]
Wang, Jia-Mei [1 ]
Sun, Jia [1 ]
Li, Chao [1 ]
Liu, Bao-Qin [1 ]
Yan, Jing [1 ]
Meng, Xiao-Na [1 ]
Wang, Hua-Qin [1 ,2 ,3 ]
机构
[1] China Med Univ, Dept Biochem & Mol Biol, Shenyang 110026, Liaoning, Peoples R China
[2] China Med Univ, Key Lab Cell Biol, Minist Publ Hlth, Shenyang, Liaoning, Peoples R China
[3] China Med Univ, Key Lab Med Cell Biol, Minist Educ, Shenyang, Liaoning, Peoples R China
[4] China Med Univ, Canc Hosp, Shenyang, Liaoning, Peoples R China
[5] Liaoning Canc Hosp & Inst, Shenyang, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
BAG3; invasion; microenvironments; PDACs; PSCs; ANTIAPOPTOTIC PROTEIN BAG3; STROMAL BIOLOGY; CANCER; PROGRESSION; EXPRESSION; MICROENVIRONMENT; THERAPY;
D O I
10.1111/jcmm.14352
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
BAG3 is constitutively expressed in multiple types of cancer cells and its high expression is associated with tumour progression and poor prognosis of PDAC. However, little is known about the role of BAG3 in the regulation of stromal microenvironment of PDAC. The current study demonstrated that beside PDAC tumour cells, BAG3 was also expressed in some activated stroma cells in PDAC tissue, as well as in activated PSCs. In addition, the current study demonstrated that BAG3 expression in PSCs was involved in maintenance of PSCs activation and promotion of PDACs invasion via releasing multiple cytokines. The current study demonstrated that BAG3-positive PSCs promoted invasion of PDACs via IL-8, MCP1, TGF-beta 2 and IGFBP2 in a paracrine manner. Furthermore, BAG3 sustained PSCs activation through IL-6, TGF-beta 2 and IGFBP2 in an autocrine manner. Thereby, the current study provides a new insight into the involvement of BAG3 in remodelling of stromal microenvironment favourable for malignant progression of PDAC, indicating that BAG3 might serve as a potential target for anti-fibrosis of PDAC.
引用
收藏
页码:5006 / 5016
页数:11
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