4.5 Article

Cancer-associated orthotopic myofibroblasts stimulates the motility of gastric carcinoma cells

Journal

CANCER SCIENCE
Volume 103, Issue 4, Pages 797-805

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1349-7006.2012.02209.x

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Funding

  1. Japan's Ministry of Education, Science, Sports, Culture and Technology
  2. Foundation for Promotion of Cancer Research [20591573, 22390262, 23390329]
  3. Grants-in-Aid for Scientific Research [23390329] Funding Source: KAKEN

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Tumor progression has been recognized as the product of evolving crosstalk between cancer cells and the surrounding stromal cells. Cancer-associated orthotopic myofibroblasts may be linked to the progression of gastric carcinomas. To understand the significance of orthotopic myofibroblasts, we examined the effects of cancer-associated orthotopic myofibroblasts on the malignant phenotype of gastric cancer cells. Three human gastric cancer cell lines (OCUM-2MD3, OCUM-12, MKN-45) and four human gastric fibroblast cell lines (cancer-associated orthotopic fibroblast [CaF]-29, CaF-33, normal orthotopic fibroblast [NF]-29, NF-33) were used. The cancer-associated orthotopic fibroblast cell lines CaF-29 and CaF-33 were established from a tumoral gastric wall, and normal orthotopic fibroblast NF-29 and NF-33 were established from a non-tumoral gastric wall. Fibroblasts that were a-smooth muscle actin-positive were defined as myofibroblasts. We examined the effects of cancer-associated orthotopic myofibroblasts on the aggressiveness of gastric cancer cells by wound-healing assay, invasion assay, and RT-PCR. The ratios of myofibroblasts in CaF-29 (33%) and CaF-33 (46%) were significantly (P similar to

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