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. 2010 Jun;15(2):272-95.
doi: 10.2478/s11658-010-0007-3. Epub 2010 Feb 25.

Inhibitor of differentiation 1 (ID1) promotes cell survival and proliferation of prostate epithelial cells

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Inhibitor of differentiation 1 (ID1) promotes cell survival and proliferation of prostate epithelial cells

Michelle Schmidt et al. Cell Mol Biol Lett. 2010 Jun.

Abstract

Id1 (inhibitor of differentiation 1) is a member of the bHLH protein family. Consistent with its role in promoting proliferation and inhibiting differentiation, Id1 expression is low or negligible in normal prostate epithelial cells but is high in prostate cancer. Ectopic expression of Id1 in normal prostate epithelial cells could therefore provide a model for understanding early events involved in initiation of prostate cancer. Over-expression of Id1 immortalized but did not transform ventral prostate epithelial cells (Id1-RPE). Immortalization was associated with decreased Cdkn2a, Cdkn1a, androgen receptor and increased Tert expression. Gene expression profiling over successive doublings was used to identify transcriptomic changes involved during immortalization (Tieg, Jun, alpha actin, Klf10, Id2) and in maintaining the immortalized phenotype (Igfbp3, Igfbp5, Mmp2, Tgfb3). Network analysis indicated that Id1 promotes cancer/tumor morphology, cell cycle and epithelial to mesenchymal transition by influencing AP1, tnf, tgfbeta, PdgfBB and estradiol pathways. During immortalization, the expression of majority of differentially expressed genes reduced over progressive doublings suggesting a decline in transcriptional regulatory mechanisms. The associated molecular/gene expression profile of Id1-RPE cells provides an opportunity to understand the molecular pathways associated with prostate epithelial cell survival and proliferation.

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References

    1. Norton J.D., Deed R.W., Craggs G., Sablitzky F. Id helix-loop-helix proteins in cell growth and differentiation. Trends Cell. Biol. 1998;8:58–65. doi: 10.1016/S0962-8924(97)01183-5. - DOI - PubMed
    1. Benezra R., Davis R.L., Lockshon D., Turner D.L., Weintraub H. The protein Id: a negative regulator of helix-loop-helix DNA binding proteins. Cell. 1990;61:49–59. doi: 10.1016/0092-8674(90)90214-Y. - DOI - PubMed
    1. Barone M.V., Pepperkok R., Peverali F.A., Philipson L. Id proteins control growth induction in mammalian cells. Proc. Natl. Acad. Sci. USA. 1994;91:4985–4988. doi: 10.1073/pnas.91.11.4985. - DOI - PMC - PubMed
    1. Hara E., Yamaguchi T., Nojima H., Ide T., Campisi J., Okayama H., Oda K. Id-related genes encoding helix-loop-helix proteins are required for G1 progression and are repressed in senescent human fibroblasts. J. Biol. Chem. 1994;269:2139–2145. - PubMed
    1. Coppe J.P., Smith A.P., Desprez P.Y. Id proteins in epithelial cells. Exp. Cell Res. 2003;285:131–145. doi: 10.1016/S0014-4827(03)00014-4. - DOI - PubMed

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