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. 2019 May 8;2019:2820853. doi: 10.1155/2019/2820853

Table 1.

Favoring effect of MSCs on tumors.

Author MSC origin Tumor model MSC: tumor cell ratio Outcomes Mechanisms
Chaturvedi P et al. [17] Human bone marrow-derived MSCs Breast( MDA-MB-231, MDA-MB-43) 1:1 coinjection Increased metastasis activation of the hypoxia-inducible factors (HIFs)

Walter, M. et al. [21] Human adipose stromal cells (ASCs) Human breast cancer cell line MCF-7 1:1 coinjection Increased migration and invasion Secretion of IL-6

Tsai, Kuo–Shu et al. [22] Human bone marrow-derived MSCs Human colorectal cancer cell line HT-29 1:100 coinjection Promoted tumor sphere formation and tumor initiation IL-6 secreted by MSCs signaled through STAT3

Zhang, Ting et al. [23] Human fetal bone marrow stem cells (hBM-MSCs) 4T1 mouse mammary tumor cell line 1:1 coinjection Increased tumor growth Neovascularization (secretion of macrophage
inflammatory protein-2, vascular endothelial growth factor, transforming growth factor-beta and IL-6)

El-Haibi, Christelle P. et al. [24] Human bone marrow-derived MSCs MDA-MB-231 and MCF7/Ras breast cancer cells 1:1 coinjection Enhanced metastasis Increased de novo production of lysyl oxidase (LOX)

Patel, Shyam A. et al. [25] Human bone marrow-derived MSCs Highly aggressive MDA-MB-231 breast adenocarcinoma, low-invasive MCF-7 breast adenocarcinoma, T47D breast adenocarcinoma, P815 murine mastocytoma 1:1 (T47D and MSCs 2 × 105 /ml each) were added in 500 μl volumes to attain a 50:1 ratio of mononuclear fractions (PBMC)/MSC and PBMC/T47D Protected breast cancer cells from immune clearance Through Tregs, inhibited NK cell and CTL functions

Chandler, Emily M. et al. [26] Human adipose-derived stem cells (ADSCs) MCF-7 and MDA-MB-231 1:1 co-injection Promoted tumorigenesis and angiogenesis Bidirectional signaling;
ADSCs differentiated into cancer-associated myofibroblasts

Gonzalez, Maria E. et al. [27] Human breast cancer metastatic sites-derived MSCs Breast cancer cell lines MDA-MB-231, MCF7, and MDA-MB-436 MSCs were orthotopically injected into the mammary fat pads (1 × 106 cells/mouse) Loss of DDR2 in MSCs impaired their ability to promote DDR2 phosphorylation in BC cells, as well as
BC cell alignment, migration, and metastasis
Reduced migration and metastasis