4.8 Article

Mesenchymal Stem Cells Promote Formation of Colorectal Tumors in Mice

Journal

GASTROENTEROLOGY
Volume 141, Issue 3, Pages 1046-1056

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2011.05.045

Keywords

Marrow Stromal Cells; Cancer Stem Cells; JAK2; Tumor Development

Funding

  1. National Science Council [3111-B-039, 96-2627-B-010-009, 97-3111-B-010-001, 99-3111-B-010-005-]
  2. Taipei Veterans General Hospital [V97C1-060, V98C1-009, V98E1-002]
  3. MD Anderson Cancer Center/China Medical University
  4. Hospital Sister Institution Fund
  5. National Yang-Ming University, Ministry of Education

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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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