Literature DB >> 29054337

Dental pulp stem cells (DPSCs) increase prostate cancer cell proliferation and migration under in vitro conditions.

Ayşegül Doğan1, Selami Demirci2, Hüseyin Apdik1, Ezgi Avşar Apdik1, Fikrettin Şahin1.   

Abstract

Cancer as a multistep and complicated disease is regulated by several molecular and cellular events. Cancer treatment could be managed at the early stages when the tumor is confined in the tissue. However, disseminated cancer cells metastasize to other body parts and generate new tumors resulting in mortality. Mesenchymal stem cells (MSCs) are found in different body parts and helps adult tissue regeneration. The role of MSCs in cancer progression has emerged as one of the important aspects in cancer biology and is the aim of interest in recent years. In the current study, effects of Dental Pulp Stem Cells (DPSCs) on PC-3 prostate cancer cell proliferation and migration were conducted by cell proliferation, apoptosis, gene expression and cell migration analysis in vitro. Condition medium (CM) obtained from DPSCs increased cell proliferation of PC-3 cells and decreased apoptosis. Either administration of CM or trans well co-culture of DPSCs increased cell migration in scratch assay, confirmed by gene expression analysis of migratory genes including fibronectin, laminin and collagen type I (Col I). Furthermore, DPSCs participated in a self-organized structure with PC-3 cells in co-culture conditions. Overall, results indicated that DPSCs could promote PC-3 cancer cell proliferation and metastasis in co-culture conditions in vitro. Published by Elsevier Ltd.

Entities:  

Keywords:  Co-culture; DPSCs; MSCs; Metastasis; Prostate cancer

Mesh:

Year:  2017        PMID: 29054337     DOI: 10.1016/j.tice.2017.10.003

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  7 in total

1.  The effects of bisphosphonates on osteonecrosis of jaw bone: a stem cell perspective.

Authors:  Hüseyin Abdik; Ezgi Avşar Abdik; Selami Demirci; Ayşegül Doğan; Duygu Turan; Fikrettin Şahin
Journal:  Mol Biol Rep       Date:  2018-12-01       Impact factor: 2.316

2.  Apelin Receptor Signaling Protects GT1-7 GnRH Neurons Against Oxidative Stress In Vitro.

Authors:  Hatice Burcu Şişli; Taha Bartu Hayal; Selinay Şenkal; Binnur Kıratlı; Derya Sağraç; Selin Seçkin; Murat Özpolat; Fikrettin Şahin; Bayram Yılmaz; Ayşegül Doğan
Journal:  Cell Mol Neurobiol       Date:  2020-09-28       Impact factor: 5.046

3.  Human ESC-derived Neuromesodermal Progenitors (NMPs) Successfully Differentiate into Mesenchymal Stem Cells (MSCs).

Authors:  Selinay Şenkal; Ayşegül Doğan; Taha Bartu Hayal; Derya Sağraç; Hatice Burcu Şişli; Ayla Burçin Asutay; Binnur Kıratlı; Engin Sümer; Albert A Rizvanov; Fikrettin Şahin
Journal:  Stem Cell Rev Rep       Date:  2021-10-20       Impact factor: 5.739

Review 4.  Interplay between mesenchymal stem cell and tumor and potential application.

Authors:  Qing Wang; Ti Li; Wei Wu; Gang Ding
Journal:  Hum Cell       Date:  2020-05-06       Impact factor: 4.174

5.  Assessing the effect of human dental pulp mesenchymal stem cell secretome on human oral, breast, and melanoma cancer cell lines.

Authors:  A Thirumal Raj; Supriya Kheur; Ramesh Bhonde; Vishnu R Mani; Hosam Ali Baeshen; Shankargouda Patil
Journal:  Saudi J Biol Sci       Date:  2021-07-14       Impact factor: 4.219

6.  Mesenchymal stem cells recruited by castration-induced inflammation activation accelerate prostate cancer hormone resistance via chemokine ligand 5 secretion.

Authors:  Yang Yu; Qingyun Zhang; Chengzhong Ma; Xue Yang; Rui Lin; Hongxiang Zhang; Yan Liu; Zhipeng Han; Jiwen Cheng
Journal:  Stem Cell Res Ther       Date:  2018-09-26       Impact factor: 6.832

Review 7.  Tumor Microenvironment.

Authors:  Borros Arneth
Journal:  Medicina (Kaunas)       Date:  2019-12-30       Impact factor: 2.430

  7 in total

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