Journal
ONCOLOGY REPORTS
Volume 33, Issue 5, Pages 2285-2290Publisher
SPANDIDOS PUBL LTD
DOI: 10.3892/or.2015.3826
Keywords
flotillin-2; breast cancer; proliferation; Akt; FOXO
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Funding
- National Natural Science Foundation of China [81101682]
- Science and Technology Planning Project of Guangzhou Municipal Health Bureau [201102A213045]
- Ph.D. Start-up Fund of Guangzhou Women and Children's Medical Center [201012]
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Lipid rafts, specialized domains in cell membranes, function as physical platforms for various molecules to coordinate a variety of signal transduction processes. Flotillin-2 (FLOT2), a marker of lipid rafts, is involved in the progression of cancer, yet the precise mechanism remains unclear. In the present study, we examined the effect of FLOT2 on cell proliferation and found that silencing endogenous FLOT2 with shRNAs inhibited proliferation of breast cancer cells. Furthermore, the antiproliferative effect of silencing FLOT2 on breast cancer cells was associated with upregulation of cyclin-dependent kinase (CDK) inhibitors p21(Cip1) and p27(Kip1). Moreover, we further demonstrated that the silencing of FLOT2 enhanced the transcriptional activity of FOXO factors by decreasing its phosphorylation through inhibiting the PI3K/Akt signaling pathway. Taken together, our results provide the first demonstration of a novel mechanism by which FLOT2 induces proliferation of breast cancer cells, and our findings suggest that FLOT2 plays an important role in oncogenesis of breast cancer and thereby may be a potential target for human breast cancer treatment.
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