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Interactions of the Hdm2/p53 and proteasome pathways may enhance the antitumor activity of bortezomib.


ABSTRACT: p53 is inactivated in many human malignancies through missense mutations or overexpression of the human homologue of Mdm2 (Hdm2), an E3 ubiquitin ligase that ubiquitinates p53, thereby promoting its proteasomal degradation. The cis-imidazoline nutlin-3 can disrupt the p53-Hdm2 interaction and activate p53, inducing apoptosis in vitro in many malignancies, including multiple myeloma (MM).We hypothesized that suppression of Hdm2-mediated p53 ubiquitination may augment sequelae of p53 accumulation caused by proteasomal inhibition. We compared the response of MM cells versus several epithelial cancer models to the proteasome inhibitor bortezomib in combination with nutlin-3.The combination of sublethal concentrations of bortezomib plus nutlin-3 induced additive cytotoxicity against bortezomib-sensitive MM cell lines. Importantly, however, in breast, prostate, colon, and thyroid (papillary, follicular, anaplastic, and medullary) carcinoma cell lines, this combination triggered synergistic cytotoxicity, and increased expression of p53, p21, Hdm2, Bax, Noxa, PUMA, and cleavage of caspase-3 and poly ADP ribose polymerase. Coculture with bone marrow stromal cells attenuated MM cell sensitivity to nutlin-3 monotherapy and was associated with evidence of suppression of p53 activity in MM cells, whereas combined bortezomib-nutlin-3 treatment maintained cytotoxicity even in the presence of bone marrow stromal cells.This differential response of MM versus epithelial carcinomas to combination of nutlin-3 with bortezomib sheds new light on the role of p53 in bortezomib-induced apoptosis. Concurrent Hdm2 inhibition with bortezomib may extend the spectrum of bortezomib applications to malignancies with currently limited sensitivity to single-agent bortezomib or, in the future, to MM patients with decreased clinical responsiveness to bortezomib-based therapy.

SUBMITTER: Ooi MG 

PROVIDER: S-EPMC3672410 | biostudies-literature | 2009 Dec

REPOSITORIES: biostudies-literature

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Interactions of the Hdm2/p53 and proteasome pathways may enhance the antitumor activity of bortezomib.

Ooi Melissa G MG   Hayden Patrick J PJ   Kotoula Vassiliki V   McMillin Douglas W DW   Charalambous Elpida E   Daskalaki Emily E   Raje Noopur S NS   Munshi Nikhil C NC   Chauhan Dharminder D   Hideshima Teru T   Buon Leutz L   Clynes Martin M   O'Gorman Peter P   Richardson Paul G PG   Mitsiades Constantine S CS   Anderson Kenneth C KC   Mitsiades Nicholas N  

Clinical cancer research : an official journal of the American Association for Cancer Research 20091124 23


<h4>Purpose</h4>p53 is inactivated in many human malignancies through missense mutations or overexpression of the human homologue of Mdm2 (Hdm2), an E3 ubiquitin ligase that ubiquitinates p53, thereby promoting its proteasomal degradation. The cis-imidazoline nutlin-3 can disrupt the p53-Hdm2 interaction and activate p53, inducing apoptosis in vitro in many malignancies, including multiple myeloma (MM).<h4>Experimental design</h4>We hypothesized that suppression of Hdm2-mediated p53 ubiquitinati  ...[more]

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