Tumor-educated mesenchymal stem cells promote pro-metastatic phenotype (347 views)
Oncotarget (ISSN: 1949-2553electronic, 1949-2553linking), 2017 Sep 22; 8(42): 73296-73311.
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Paper type: Journal Article, Review,
Impact factor: 5.168, 5-year impact factor: 5.312
Url: Not available.
Keywords: Epithelial-Mesenchymal Transition, Mesenchymal Stem Cells, Metastatic Phenotype, Tumor Microenvironment,
Affiliations:
*** IBB - CNR ***
Institute of Biostructures and Bioimaging (IBB), National Research Council (CNR), Naples, Italy., Department of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.,
Department of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.
References:
Not available.
Oncotarget (ISSN: 1949-2553electronic, 1949-2553linking), 2017 Sep 22; 8(42): 73296-73311.
Export to BibTeX Export to EndNote
Paper type: Journal Article, Review,
Impact factor: 5.168, 5-year impact factor: 5.312
Url: Not available.
Keywords: Epithelial-Mesenchymal Transition, Mesenchymal Stem Cells, Metastatic Phenotype, Tumor Microenvironment,
Affiliations:
*** IBB - CNR ***
Institute of Biostructures and Bioimaging (IBB), National Research Council (CNR), Naples, Italy., Department of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.,
Department of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.
References:
Not available.
Tumor-educated mesenchymal stem cells promote pro-metastatic phenotype
Multipotent mesenchymal stem cells (MSCs) are recruited into tumor microenvironment in response to multiple signals produced by cancer cells. Molecules involved in their homing to tumors are the same inflammatory mediators produced by injured tissues: chemokines, cytokines and growth factors. When MSCs arrive into the tumor microenvironment these are "educated" to have pro-metastatic behaviour. Firstly, they promote cancer immunosuppression modulating both innate and adaptive immune systems. Moreover, tumor associated-MSCs trans-differentiating into cancer-associated fibroblasts can induce epithelial-mesenchymal-transition program in tumor cells. This process determinates a more aggressive phenotype of cancer cells by increasing their motility and invasiveness and favoring their dissemination to distant sites. In addition, MSCs are involved in the formation and modelling of pre-metastatic niches creating a supportive environment for colonization of circulating tumor cells. The development of novel therapeutic approaches targeting the different functions of MSCs in promoting tumor progression as well as the mechanisms underlying their activities could enhance the efficacy of conventional and immune anti-cancer therapies. Furthermore, many studies report the use of MSCs engineered to express different genes or as vehicle to specifically deliver novel drugs to tumors exploiting their strong tropism. Importantly, this approach can enhance local therapeutic efficacy and reduce the risk of systemic side effects.
Multipotent mesenchymal stem cells (MSCs) are recruited into tumor microenvironment in response to multiple signals produced by cancer cells. Molecules involved in their homing to tumors are the same inflammatory mediators produced by injured tissues: chemokines, cytokines and growth factors. When MSCs arrive into the tumor microenvironment these are "educated" to have pro-metastatic behaviour. Firstly, they promote cancer immunosuppression modulating both innate and adaptive immune systems. Moreover, tumor associated-MSCs trans-differentiating into cancer-associated fibroblasts can induce epithelial-mesenchymal-transition program in tumor cells. This process determinates a more aggressive phenotype of cancer cells by increasing their motility and invasiveness and favoring their dissemination to distant sites. In addition, MSCs are involved in the formation and modelling of pre-metastatic niches creating a supportive environment for colonization of circulating tumor cells. The development of novel therapeutic approaches targeting the different functions of MSCs in promoting tumor progression as well as the mechanisms underlying their activities could enhance the efficacy of conventional and immune anti-cancer therapies. Furthermore, many studies report the use of MSCs engineered to express different genes or as vehicle to specifically deliver novel drugs to tumors exploiting their strong tropism. Importantly, this approach can enhance local therapeutic efficacy and reduce the risk of systemic side effects.
Tumor-educated mesenchymal stem cells promote pro-metastatic phenotype
| ▼ Molecular imaging for personalized therapy in oncology |
| ▼ Imaging Tumor Acidosis |
Tumor-educated mesenchymal stem cells promote pro-metastatic phenotype
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* Molecular imaging of tumor microenvironment: Challenges and perspectives (685 views)
Q J Nucl Med Mol Im (ISSN: 1824-4785, 1824-4478, 1824-4785linking), 2010 Jun; 54(3): 249-258.
Impact Factor: 1.724
View Export to BibTeX Export to EndNote
27 Records (25 excluding Abstracts).
Total impact factor: 148.537 (138.027 excluding Abstracts).
Total 5 year impact factor: 78.765 (68.072 excluding Abstracts).
Total impact factor: 148.537 (138.027 excluding Abstracts).
Total 5 year impact factor: 78.765 (68.072 excluding Abstracts).
347 views. Last view on Tuesday 23 April 2024, 21:34:53
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