Novel proteasome inhibitor delanzomib sensitizes cervical cancer cells to doxorubicin-induced apoptosis via stabilizing tumor suppressor proteins in the p53 pathway Journal Article


Authors: Guo, K. Y.; Han, L.; Li, X.; Yang, A. V.; Lu, J.; Guan, S.; Li, H.; Yu, Y.; Zhao, Y.; Yang, J.; Zhang, H.
Article Title: Novel proteasome inhibitor delanzomib sensitizes cervical cancer cells to doxorubicin-induced apoptosis via stabilizing tumor suppressor proteins in the p53 pathway
Abstract: Cervical cancer, the third most commonly occurring cancer, is the second leading cause of cancer related mortality among women. Aberrant ubiquitination and proteasome activity, both human papillomavirus and tumor derived, have been shown to contribute to tumor angiogenesis, proliferation, and invasion in many cancers, including cervical cancer. Thus, small molecule proteasome inhibitors are a potential and strategic treatment option for cervical cancer. In this study, novel proteasome inhibitor delanzomib (CEP-18770) exhibited potent pro-apoptotic and cytotoxic effects on a panel of cervical cancer cell lines by blocking proteasomal activity. Delanzomib also significantly sensitized cervical cancer cells to treatment of doxorubicin (Dox), a traditional chemotherapeutic agent. Furthermore, proteasome inhibition revealed stabilization of p53 and p53 transcriptional targets and induction of p38/JNK phosphorylation. Additionally, delanzomib worked synergistically with Dox to further upregulate p53 and its downstream targets and enhanced Dox-induced p38 phosphorylation. Our study strongly supports the 26S proteasome as a potential therapeutic target in cervical cancer and proteasome inhibition by delanzomib may be a potential treatment strategy for cervical cancer patients. © Guo et al.
Keywords: signal transduction; mitogen activated protein kinase; controlled study; protein phosphorylation; human cell; doxorubicin; drug potentiation; flow cytometry; cell proliferation; cell viability; apoptosis; proteasome; protein stability; antineoplastic activity; cytotoxicity; drug potency; autophosphorylation; protein p53; morphology; ubiquitination; immunoblotting; upregulation; anchorage independent growth; protein cleavage; p53; cervical cancer; cytochrome c; colony formation; chemosensitization; human; article; delanzomib; cervical cancer cell line
Journal Title: Oncotarget
Volume: 8
Issue: 69
ISSN: 1949-2553
Publisher: Impact Journals  
Date Published: 2017-12-26
Start Page: 114123
End Page: 114135
Language: English
DOI: 10.18632/oncotarget.23166
PROVIDER: scopus
PMCID: PMC5768391
PUBMED: 29371974
DOI/URL:
Notes: Article -- Export Date: 1 February 2018 -- Source: Scopus
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  1. Hong Zhang
    54 Zhang