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Mesenchymal stem cells promote formation of colorectal tumors in mice. | LitMetric

AI Article Synopsis

  • * By injecting human colorectal cancer cells alone, MSCs alone, or a mix of both into mice, researchers found that even a small number of specific cancer cells could form tumors when combined with MSCs.
  • * The study revealed that MSCs secrete interleukin-6 (IL-6), which activates a signaling pathway (STAT3) in cancer cells, enhancing tumor initiation; blocking IL-6 or STAT3 could potentially be a strategy for colorectal cancer treatment.

Article Abstract

Background & Aims: Tumor-initiating cells are a subset of tumor cells with the ability to form new tumors; however, they account for less than 0.001% of the cells in colorectal or other types of tumors. Mesenchymal stem cells (MSCs) integrate into the colorectal tumor stroma; we investigated their involvement in tumor initiation.

Methods: Human colorectal cancer cells, MSCs, and a mixture of both cell types were injected subcutaneously into immunodeficient mice. We compared the ability of each injection to form tumors and investigated the signaling pathway involved in tumor initiation.

Results: A small number (≤ 10) of unsorted, CD133⁻, CD166⁻, epithelial cell adhesion molecule⁻(EpCAM⁻), or CD133⁻/CD166⁻/EpCAM⁻ colorectal cancer cells, when mixed with otherwise nontumorigenic MSCs, formed tumors in mice. Secretion of interleukin (IL)-6 by MSCs increased the expression of CD133 and activation of Janus kinase 2-signal transducer and activator of transcription 3 (STAT3) in the cancer cells, and promoted sphere and tumor formation. An antibody against IL-6 or lentiviral-mediated transduction of an interfering RNA against IL-6 in MSCs or STAT3 in cancer cells prevented the ability of MSCs to promote sphere formation and tumor initiation.

Conclusions: IL-6, secreted by MSCs, signals through STAT3 to increase the numbers of colorectal tumor-initiating cells and promote tumor formation. Reagents developed to disrupt this process might be developed to treat patients with colorectal cancer.

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Source
http://dx.doi.org/10.1053/j.gastro.2011.05.045DOI Listing

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