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Comment
. 2008 Feb 8;132(3):339-41.
doi: 10.1016/j.cell.2008.01.022.

Secreting tumor suppression

Affiliations
Comment

Secreting tumor suppression

Yuchen Chien et al. Cell. .

Abstract

Cellular senescence limits the proliferative capacity of damaged cells and thereby acts as an intrinsic mechanism of tumor suppression. In this issue, Wajapeyee et al. (2008) identify insulin growth factor binding protein 7 (IGFBP7) as a secreted factor that mediates senescence induced by oncogenic BRAF in normal melanocytes. In addition, IGFBP7 triggers apoptosis in cells that have progressed to melanoma, suggesting a new approach for melanoma treatment.

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Figures

Figure 1
Figure 1. IGFBP7 and BRAF-Induced Cellular Senescence
Early during melanoma progression, melanocytes acquire BRAF mutations that stimulate proliferation but also trigger senescence, in part, via enhanced secretion of insulin growth factor binding protein 7 (IGFBP7). Silencing of IGFBP7 enables BRAF-expressing melanocytes to escape senescence and progress toward melanoma. The resulting melanoma cells remain sensitive to the induction of apoptosis by addition of IGFBP7.

Comment on

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