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Adipose-Derived Stem Cells Inhibited the Proliferation of Bladder Tumor Cells by S Phase Arrest and Wnt/β-Catenin Pathway
Author(s) -
Tao Wang,
Xi Yu,
Jian Lin,
Cong Qin,
Tao Bai,
Tao Xu,
Lei Wang,
Xiuheng Liu,
Shenglan Li
Publication year - 2019
Publication title -
cellular reprogramming
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.517
H-Index - 60
eISSN - 2152-4998
pISSN - 2152-4971
DOI - 10.1089/cell.2019.0047
Subject(s) - stem cell , wnt signaling pathway , biology , adipose tissue , cell cycle , apoptosis , microbiology and biotechnology , cell growth , cancer research , signal transduction , endocrinology , biochemistry
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/β-catenin pathway. These findings demonstrated that ADSCs could inhibit the proliferation of BT cells via secretory factors.

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