Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor

The aim of this study was to determine the effect of human adipose derived stem cells (ADSCs) on the viability and apoptosis of human bladder cancer cells. EJ and T24 cells were cocultured with ADSCs or cultured with conditioned medium of ADSCs (ADSC-CM), respectively. The cell counting and colony f...

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Main Authors: Xi Yu, Boxing Su, Peng Ge, Zicheng Wang, Sen Li, Bingwei Huang, Yanqing Gong, Jian Lin
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2015/619290
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spelling doaj-04dd4ab319514719a96261b0e94574ae2020-11-24T23:55:34ZengHindawi LimitedStem Cells International1687-966X1687-96782015-01-01201510.1155/2015/619290619290Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder TumorXi Yu0Boxing Su1Peng Ge2Zicheng Wang3Sen Li4Bingwei Huang5Yanqing Gong6Jian Lin7National Urological Cancer Center, Beijing 100034, ChinaNational Urological Cancer Center, Beijing 100034, ChinaNational Urological Cancer Center, Beijing 100034, ChinaNational Urological Cancer Center, Beijing 100034, ChinaBeijing Shunyi District Hospital, Beijing 101300, ChinaQinzhou First People’s Hospital, Qinzhou 535000, ChinaNational Urological Cancer Center, Beijing 100034, ChinaNational Urological Cancer Center, Beijing 100034, ChinaThe aim of this study was to determine the effect of human adipose derived stem cells (ADSCs) on the viability and apoptosis of human bladder cancer cells. EJ and T24 cells were cocultured with ADSCs or cultured with conditioned medium of ADSCs (ADSC-CM), respectively. The cell counting and colony formation assay showed ADSCs inhibited the proliferation of EJ and T24 cells. Cell viability assessment revealed that the secretions of ADSCs, in the form of conditioned medium, were able to decrease cancer cell viability. Wound-healing assay suggested ADSC-CM suppressed migration of T24 and EJ cells. Moreover, the results of the flow cytometry indicated that ADSC-CM was capable of inducing apoptosis of T24 cells and inducing S phase cell cycle arrest. Western blot revealed ADSC-CM increased the expression of cleaved caspase-3 and cleaved PARP, indicating that ADSC-CM induced apoptosis in a caspase-dependent way. PTEN/PI3K/Akt pathway and Bcl-2 family proteins were involved in the mechanism of this reaction. Our study indicated that ADSCs may provide a promising and practicable manner for bladder tumor therapy.http://dx.doi.org/10.1155/2015/619290
collection DOAJ
language English
format Article
sources DOAJ
author Xi Yu
Boxing Su
Peng Ge
Zicheng Wang
Sen Li
Bingwei Huang
Yanqing Gong
Jian Lin
spellingShingle Xi Yu
Boxing Su
Peng Ge
Zicheng Wang
Sen Li
Bingwei Huang
Yanqing Gong
Jian Lin
Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor
Stem Cells International
author_facet Xi Yu
Boxing Su
Peng Ge
Zicheng Wang
Sen Li
Bingwei Huang
Yanqing Gong
Jian Lin
author_sort Xi Yu
title Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor
title_short Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor
title_full Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor
title_fullStr Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor
title_full_unstemmed Human Adipose Derived Stem Cells Induced Cell Apoptosis and S Phase Arrest in Bladder Tumor
title_sort human adipose derived stem cells induced cell apoptosis and s phase arrest in bladder tumor
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2015-01-01
description The aim of this study was to determine the effect of human adipose derived stem cells (ADSCs) on the viability and apoptosis of human bladder cancer cells. EJ and T24 cells were cocultured with ADSCs or cultured with conditioned medium of ADSCs (ADSC-CM), respectively. The cell counting and colony formation assay showed ADSCs inhibited the proliferation of EJ and T24 cells. Cell viability assessment revealed that the secretions of ADSCs, in the form of conditioned medium, were able to decrease cancer cell viability. Wound-healing assay suggested ADSC-CM suppressed migration of T24 and EJ cells. Moreover, the results of the flow cytometry indicated that ADSC-CM was capable of inducing apoptosis of T24 cells and inducing S phase cell cycle arrest. Western blot revealed ADSC-CM increased the expression of cleaved caspase-3 and cleaved PARP, indicating that ADSC-CM induced apoptosis in a caspase-dependent way. PTEN/PI3K/Akt pathway and Bcl-2 family proteins were involved in the mechanism of this reaction. Our study indicated that ADSCs may provide a promising and practicable manner for bladder tumor therapy.
url http://dx.doi.org/10.1155/2015/619290
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