Adipose-Derived Stem Cells Inhibited the Proliferation of Bladder Tumor Cells by S Phase Arrest and Wnt/β-Catenin Pathway

被引:12
|
作者
Wang, Tao [1 ]
Yu, Xi [1 ]
Lin, Jian [2 ]
Qin, Cong [1 ]
Bai, Tao [1 ]
Xu, Tao [1 ]
Wang, Lei [1 ]
Liu, Xiuheng [1 ]
Li, Shenglan [3 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Urol, 99 Zhang Zhidong Rd, Wuhan 430060, Hubei, Peoples R China
[2] Peking Univ, Hosp 1, Dept Urol, Beijing, Peoples R China
[3] Wuhan Univ, Renmin Hosp, Dept Radiog, 99 Zhang Zhidong Rd, Wuhan 430060, Hubei, Peoples R China
关键词
adipose-derived stem cell; bladder tumor; S phase arrest; caspase3; 7; Wnt; beta-catenin; STROMAL CELLS; CYCLIN-A; CANCER; ACTIVATION; DIAGNOSIS; GROWTH; TRAIL; BETA;
D O I
10.1089/cell.2019.0047
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Adipose-derived stem cells (ADSCs), which are present in most organs and tissues, were evaluated as a novel medium for stem cell therapy. In this study, we investigated the effects and underlying mechanisms of ADSCs in bladder tumor (BT) cells. SV-HUC, T24, and EJ cells were cultured with ADSCs and conditioned medium from ADSCs (ADSC-CM). We observed that in routine culture, ADSCs significantly inhibited the proliferation of T24 and EJ cells in a dose-dependent manner. In addition, ADSC-CM attenuated the viability of T24 and EJ cells in a dose-dependent manner. Cell cycle analysis indicated that ADSC-CM was capable of inducing T24 and EJ cells S phase arrest and downregulating the expression of CDK 1, whereas the expression of cyclin A was increased. ADSC-CM could induce apoptosis in T24 cells. The mechanism of this effect likely involved the caspase3/7 pathway and Wnt/beta-catenin pathway. These findings demonstrated that ADSCs could inhibit the proliferation of BT cells via secretory factors.
引用
收藏
页码:331 / 338
页数:8
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