AI Article Synopsis

  • The interaction between cancer cells and fibroblasts in the tumor microenvironment is crucial for cancer progression, though the mechanisms are still not fully understood.
  • Fibroblasts significantly modulate the proteomic profile of breast cancer cells (8701-BC), particularly influencing cytoskeleton proteins and glycolytic enzymes.
  • The study found that fibroblast stimulation not only boosted the proliferation and invasion of cancer cells but also increased the expression of the c-Myc oncogene, indicating a potential enhancement of cancer malignancy.

Article Abstract

It is now widely recognized that the cross-talk between cancer and stromal cells may play a crucial role in cancer progression. However, little is known about the complex underlying molecular mechanisms that occur within the tumor microenvironment. Fibroblasts are the major stromal cells with multiple roles, especially toward both the extracellular matrix and the neighboring cell population, including neoplastic cells. Consequently, proteomic analyses would provide a wider resource for a better understanding of the potential modulating effects exerted by fibroblasts on cancer cells. In this article we describe the effects of fibroblast stimulation on the breast cancer cell line (8701-BC) proteomics, using a trans-well coculture system. Our results clearly indicate that fibroblasts induce considerable proteomic modulations on 8701-BC, mainly in the cytoskeleton proteins and glycolytic enzymes. Additionally, fibroblast-conditioned medium increased neoplastic cell proliferation and invasion with a concurrent upregulation of the c-Myc oncogene. Collectively these results suggest that fibroblast stimulation may enhance the malignant potential of breast cancer cells in vitro.

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Source
http://dx.doi.org/10.3109/03008200903100651DOI Listing

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