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Mesenchymal stem cells as a double-edged sword in suppression or progression of solid tumor cells.

作者信息

Norozi Fatemeh, Ahmadzadeh Ahmad, Shahrabi Saeid, Vosoughi Tina, Saki Najmaldin

机构信息

Health Research Institute, Research Center of Thalassemia & Hemoglobinopathy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

Department of biochemistry and hematology, Faculty of Medicine, Semnan University of medical sciences, Semnan, Iran.

出版信息

Tumour Biol. 2016 Sep;37(9):11679-11689. doi: 10.1007/s13277-016-5187-7. Epub 2016 Jul 20.


DOI:10.1007/s13277-016-5187-7
PMID:27440203
Abstract

Tumor cells are able to attract mesenchymal stem cells (MSCs) to primary tumor site. On the other hand, MSCs secrete various factors to attract tumor cells towards BM. In this review, in addition to assessment of MSCs function at tumor sites and their impact on growth and metastasis of tumor cells, the importance of MSC in attraction of malignant cells to BM and their involvement in drug resistance of tumor cells have also been studied. Relevant literature was identified by a PubMed search (2000-2015) of English-language literature using the terms mesenchymal stem cells, cancer cell, metastasis, and tumor microenvironment. MSCs migrate towards tumor microenvironment and are involved in both pro-tumorigenic and antitumorigenic functions. The dual function of MSCs at tumor sites is dependent upon a variety of factors, including the type and origin of MSCs, the cancer cell line under study, in vivo or in vitro conditions, the factors secreted by MSCs and interactions between MSCs, host immune cells and cancer cells. Therefore, MSCs can be regarded both as friends and enemies of cancer cells. Although the role of a number of pathways, including IL-6/STAT3 pathway, has been indicated in controlling the interaction between MSCs and tumor cells, other mechanisms by which MSCs can control the tumor cells are not clear yet. A better understanding of these mechanisms through further studies can determine the exact role of MSCs in cancer progression and identify them as important therapeutic agents or targets.

摘要

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本文引用的文献

[1]
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Oncol Lett. 2016-2

[2]
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[3]
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Redox Biol. 2015-12

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Clin Transl Oncol. 2016-2

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bFGF Promotes the Migration of Human Dermal Fibroblasts under Diabetic Conditions through Reactive Oxygen Species Production via the PI3K/Akt-Rac1- JNK Pathways.

Int J Biol Sci. 2015-6-1

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Bonekey Rep. 2015-5-20

[8]
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Front Endocrinol (Lausanne). 2015-5-15

[9]
Potential of Mesenchymal Stem Cell based application in Cancer.

Int J Hematol Oncol Stem Cell Res. 2015-4-1

[10]
Could cancer and infection be adverse effects of mesenchymal stromal cell therapy?

World J Stem Cells. 2015-3-26

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