Importance of the origin of mesenchymal (stem) stromal cells in cancer biology: "alliance" or "war" in intercellular signals

被引:26
作者
Eiro, Noemi [1 ]
Fraile, Maria [1 ]
Fernandez-Francos, Silvia [1 ]
Sanchez, Rosario [2 ]
Costa, Luis A. [1 ]
Vizoso, Francisco J. [1 ,2 ]
机构
[1] Fdn Hosp Jove, Unit Res, Avda Eduardo Castro 161, Gijon 33290, Asturias, Spain
[2] Fdn Hosp Jove, Dept Surg, Gijon 33290, Asturias, Spain
关键词
Tumor microenvironment; Uterine mesenchymal stem cell; Cancer associated fibroblasts; Macrophage associated cancer; PROMOTE TUMOR-GROWTH; FREE LYSATE INHIBIT; BONE-MARROW; BREAST-CANCER; CONDITIONED MEDIUM; ADIPOSE-TISSUE; IN-VITRO; EXTRACELLULAR VESICLES; PROSTATE-CANCER; INTERFERON-BETA;
D O I
10.1186/s13578-021-00620-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem cells (MSCs) play a central role in the intercellular signaling within the tumor microenvironment (TME), exchanging signals with cancer cells and tumor stromal cells, such as cancer-associated fibroblasts and inflammatory mononuclear cells. Research attributes both pro-tumor and anti-tumor actions to MSCs; however, evidence indicates that MSCs specific effect on the tumor depends on the source of the MSCs and the type of tumor. There are consistent data proving that MSCs from reproductive tissues, such as the uterus, umbilical cord or placenta, have potent anti-tumor effects and tropism towards tumor tissues. More interestingly, products derived from MSCs, such as secretome or extracellular vesicles, seem to reproduce the effects of their parental cells, showing a potential advantage for clinical treatments by avoiding the drawbacks associated with cell therapy. Given these perspectives, it appears necessary new research to optimize the production, safety and antitumor potency of the products derived from the MSCs suitable for oncological therapies.
引用
收藏
页数:19
相关论文
共 205 条
[91]   Stem Cell-Based Cell Carrier for Targeted Oncolytic Virotherapy: Translational Opportunity and Open Questions [J].
Kim, Janice ;
Hall, Robert R., III ;
Lesniak, Maciej S. ;
Ahmed, Atique U. .
VIRUSES-BASEL, 2015, 7 (12) :6200-6217
[92]   Mesenchymal Stem Cells as Vectors for Lung Cancer Therapy [J].
Kolluri, Krishna K. ;
Laurent, Geoff J. ;
Janes, Sam M. .
RESPIRATION, 2013, 85 (06) :443-451
[93]   Exosome mimetics: a novel class of drug delivery systems [J].
Kooijmans, Sander A. A. ;
Vader, Pieter ;
van Dommelen, Susan M. ;
van Solinge, Wouter W. ;
Schiffelers, Raymond M. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :1525-1541
[94]  
Lai Ruenn Chai, 2012, Int J Proteomics, V2012, P971907, DOI 10.1155/2012/971907
[95]   Mesenchymal Stem/Stromal Cells Protect against Autoimmunity via CCL2-Dependent Recruitment of Myeloid-Derived Suppressor Cells [J].
Lee, Hyun Ju ;
Ko, Jung Hwa ;
Jeong, Hyun Jeong ;
Ko, Ah Young ;
Kim, Mee Kum ;
Wee, Won Ryang ;
Yoon, Sun-ok ;
Oh, Joo Youn .
JOURNAL OF IMMUNOLOGY, 2015, 194 (08) :3634-+
[96]   Inhibition of TGF-β/Smad Signaling by BAMBI Blocks Differentiation of Human Mesenchymal Stem Cells to Carcinoma-Associated Fibroblasts and Abolishes Their Protumor Effects [J].
Lei Shangguan ;
Ti, Xinyu ;
Krause, Ulf ;
Hai, Bo ;
Zhao, Yanqiu ;
Yang, Zhenhua ;
Liu, Fei .
STEM CELLS, 2012, 30 (12) :2810-2819
[97]   Molecular imaging for assessment of mesenchymal stem cells mediated breast cancer therapy [J].
Leng, Liang ;
Wang, Yuebing ;
He, Ningning ;
Wang, Di ;
Zhao, Qianjie ;
Feng, Guowei ;
Su, Weijun ;
Xu, Yang ;
Han, Zhongchao ;
Kong, Deling ;
Cheng, Zhen ;
Xiang, Rong ;
Li, Zongjin .
BIOMATERIALS, 2014, 35 (19) :5162-5170
[98]   A prodrug-doped cellular Trojan Horse for the potential treatment of prostate cancer [J].
Levy, Oren ;
Brennen, W. Nathaniel ;
Han, Edward ;
Rosen, David Marc ;
Musabeyezu, Juliet ;
Safaee, Helia ;
Ranganath, Sudhir ;
Ngai, Jessica ;
Heinelt, Martina ;
Milton, Yuka ;
Wang, Hao ;
Bhagchandani, Sachin H. ;
Joshi, Nitin ;
Bhowmick, Neil ;
Denmeade, Samuel R. ;
Isaacs, John T. ;
Karp, Jeffrey M. .
BIOMATERIALS, 2016, 91 :140-150
[99]   mRNA-engineered mesenchymal stem cells for targeted delivery of interleukin-10 to sites of inflammation [J].
Levy, Oren ;
Zhao, Weian ;
Mortensen, Luke J. ;
LeBlanc, Sarah ;
Tsang, Kyle ;
Fu, Moyu ;
Phillips, Joseph A. ;
Sagar, Vinay ;
Anandakumaran, Priya ;
Ngai, Jessica ;
Cui, Cheryl H. ;
Eimon, Peter ;
Angel, Matthew ;
Lin, Charles P. ;
Yanik, Mehmet Fatih ;
Karp, Jeffrey M. .
BLOOD, 2013, 122 (14) :E23-E32
[100]   Human Wharton's Jelly Stem Cells, its Conditioned Medium and Cell-Free Lysate Inhibit the Growth of Human Lymphoma Cells [J].
Lin, Hao Daniel ;
Fong, Chui Yee ;
Biswas, Arijit ;
Choolani, Mahesh ;
Bongso, Ariff .
STEM CELL REVIEWS AND REPORTS, 2014, 10 (04) :573-586