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Adipose-Derived Stem Cells Facilitate Ovarian Tumor Growth and Metastasis by Promoting Epithelial to Mesenchymal Transition Through Activating the TGF-β Pathway

Xiaowu Liu, Guannan Zhao, Xueyun Huo, Yaohong Wang, Gábor Tigyi, Bing‐Mei Zhu, Junming Yue, Wenjing Zhang

2021Frontiers in Oncology19 citationsDOIOpen Access PDF

Abstract

Adipose-derived stem cells (ADSC) are multipotent mesenchymal stem cells derived from adipose tissues and are capable of differentiating into multiple cell types in the tumor microenvironment (TME). The roles of ADSC in ovarian cancer (OC) metastasis are still not well defined. To understand whether ADSC contributes to ovarian tumor metastasis, we examined epithelial to mesenchymal transition (EMT) markers in OC cells following the treatment of the ADSC-conditioned medium (ADSC-CM). ADSC-CM promotes EMT in OC cells. Functionally, ADSC-CM promotes OC cell proliferation, survival, migration, and invasion. We further demonstrated that ADSC-CM induced EMT via TGF-β growth factor secretion from ADSC and the ensuing activation of the TGF-β pathway. ADSC-CM-induced EMT in OC cells was reversible by the TGF-β inhibitor SB431542 treatment. Using an orthotopic OC mouse model, we also provide the experimental evidence that ADSC contributes to ovarian tumor growth and metastasis by promoting EMT through activating the TGF-β pathway. Taken together, our data indicate that targeting ADSC using the TGF-β inhibitor has the therapeutic potential in blocking the EMT and OC metastasis.

Topics & Concepts

Cancer researchMesenchymal stem cellEpithelial–mesenchymal transitionAdipose tissueMetastasisOvarian cancerStem cellTransforming growth factorTumor microenvironmentCancer stem cellBiologyCancerMedicinePathologyInternal medicineCell biologyEndocrinologyTumor cellsCancer Cells and MetastasisMesenchymal stem cell researchCancer, Hypoxia, and Metabolism