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. 2012 Apr 15;11(8):1486.
doi: 10.4161/cc.20048.

pRb or its cousins: who controls the family business?

pRb or its cousins: who controls the family business?

Koji Itahana et al. Cell Cycle. .

Abstract

Comment on: Bazarov A, et al. Cell Cycle 2012; 11:1008–1013

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Figures

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Figure 1. Contribution of pRb family proteins to p16-mediated senescence in breast cancer cells and HMECs. Knockdown of each of the three pRb family proteins in breast cancer cells does not abrogate ectopic p16-induced senescence, suggesting that either two of pRb family proteins can compensate for the loss of each pRb family proteins or all three of pRb family proteins play an additive role in p16-mediated senescence in breast cancer cells. On the other hand, knockdown of pRb, but not of p107 or p130, abrogates HMEC senescence, suggesting a non-redundant critical role for pRb in senescence of HMECs. However, the knockdown of either p107 or p130, in conjunction with pRb depletion, abrogates HMEC senescence more efficiently than pRb knockdown alone. This suggests a supporting role for p107 and p130 in maintaining HMEC senescence.

Comment in

  • Bazarov A, et al. The specific role of pRb in p16 (INK4A) -mediated arrest of normal and malignant human breast cells. Cell cycle. 2012;11 doi: 10.4161/cc.11.5.19492.

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