Contrasting Views on the Role of Mesenchymal Stromal/Stem Cells in Tumour Growth: A Systematic Review of Experimental Design

被引:9
作者
Oloyo, Ahmed Kolade [1 ,2 ,3 ]
Ambele, Melvin Anyasi [1 ,2 ,4 ]
Pepper, Michael Sean [1 ,2 ]
机构
[1] Univ Pretoria, Inst Cellular & Mol Med, Dept Immunol, Pretoria, South Africa
[2] Univ Pretoria, SAMRC Extramural Unit Stem Cell Res & Therapy, Fac Hlth Sci, Pretoria, South Africa
[3] Univ Lagos, Dept Physiol, Fac Basic Med Sci, Coll Med, Lagos, Nigeria
[4] Univ Pretoria, Dept Oral Pathol & Oral Biol, Sch Dent, Fac Hlth Sci, Pretoria, South Africa
来源
STEM CELLS: BIOLOGY AND ENGINEERING | 2018年 / 1083卷
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
Cancer; Mesenchymal stem cell; Syngeneic; Tumour; Xenogeneic; BREAST-CANCER CELLS; HUMAN BONE-MARROW; STEM-CELLS; ADIPOSE-TISSUE; IN-VITRO; CONDITIONED MEDIUM; POTENTIAL ROLE; GENE-THERAPY; PARACRINE; PROGRESSION;
D O I
10.1007/5584_2017_118
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The effect of mesenchymal stromal/stem cells (MSCs) on tumour growth remains controversial. Experimental evidence supports both an inhibitory and a stimulatory effect. We have assessed factors responsible for the contrasting effects of MSCs on tumour growth by doing a meta-analysis of existing literature between 2000 and May 2017. We assessed 183 original research articles comprising 338 experiments. We considered (a) in vivo and in vitro experiments, (b) whether in vivo studies were syngeneic or xenogeneic, and (c) if animals were immune competent or deficient. Furthermore, the sources and types of cancer cells and MSCs were considered together with modes of cancer induction and MSC administration. 56% of all 338 experiments reported that MSCs promote tumour growth. 78% and 79% of all experiments sourced human MSCs and cancer cells, respectively. MSCs were used in their naive and engineered form in 86% and 14% of experiments, respectively, the latter to produce factors that could alter either their activity or that of the tumour. 53% of all experiments were conducted in vitro with 60% exposing cancer cells to MSCs via coculture. Of all in vivo experiments, 79% were xenogeneic and 63% were conducted in immune-competent animals. Tumour growth was inhibited in 80% of experiments that used umbilical cord-derived MSCs, whereas tumour growth was promoted in 64% and 57% of experiments that used bone marrow- and adipose tissue-derived MSCs, respectively. This contrasting effect of MSCs on tumour growth observed under different experimental conditions may reflect differences in experimental design. This analysis calls for careful consideration of experimental design given the large number of MSC clinical trials currently underway.
引用
收藏
页码:103 / 124
页数:22
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