The rapamycin analog CCI-779 is a potent inhibitor of pancreatic cancer cell proliferation - PubMed (original) (raw)
The rapamycin analog CCI-779 is a potent inhibitor of pancreatic cancer cell proliferation
Takayuki Asano et al. Biochem Biophys Res Commun. 2005.
Abstract
We present immunohistochemical evidence that the mTOR/p70s6k pathway is activated in pancreatic tumors and show that the mTOR inhibitor and rapamycin analog CCI-779 potently suppresses the proliferation of pancreatic cancer cells. Consistent with a recent study, CCI-779 increased c-Jun phosphorylation (Ser63) in a dose- and time-dependent manner, and induced apoptosis in p53-defective BxPC-3 cells. In contrast to the study, however, we observed that CCI-779 concomitantly increased c-Jun protein levels and that its ability to induce apoptosis might not require the activated c-Jun. Furthermore, CCI-779 neither induced c-Jun phosphorylation in other p53-defective pancreatic cancer cells (MiaPaCa-2) nor inhibited their proliferation. c-Jun, in fact, appeared to be partly responsible for the resistance of MiaPaCa-2 cells to CCI-779. Together, these results indicate a complex role for c-Jun in cellular responses to CCI-779 and provide an important basis for investigating CCI-779 further as a potential therapeutic agent for pancreatic tumors.
Similar articles
- Mammalian target of rapamycin inhibitors rapamycin and RAD001 (everolimus) induce anti-proliferative effects in GH-secreting pituitary tumor cells in vitro.
Gorshtein A, Rubinfeld H, Kendler E, Theodoropoulou M, Cerovac V, Stalla GK, Cohen ZR, Hadani M, Shimon I. Gorshtein A, et al. Endocr Relat Cancer. 2009 Sep;16(3):1017-27. doi: 10.1677/ERC-08-0269. Epub 2009 Jun 9. Endocr Relat Cancer. 2009. PMID: 19509067 - A new pharmacologic action of CCI-779 involves FKBP12-independent inhibition of mTOR kinase activity and profound repression of global protein synthesis.
Shor B, Zhang WG, Toral-Barza L, Lucas J, Abraham RT, Gibbons JJ, Yu K. Shor B, et al. Cancer Res. 2008 Apr 15;68(8):2934-43. doi: 10.1158/0008-5472.CAN-07-6487. Cancer Res. 2008. PMID: 18413763 - Role of RAF/MEK/ERK pathway, p-STAT-3 and Mcl-1 in sorafenib activity in human pancreatic cancer cell lines.
Ulivi P, Arienti C, Amadori D, Fabbri F, Carloni S, Tesei A, Vannini I, Silvestrini R, Zoli W. Ulivi P, et al. J Cell Physiol. 2009 Jul;220(1):214-21. doi: 10.1002/jcp.21753. J Cell Physiol. 2009. PMID: 19288493 - Mammalian target of rapamycin is a promising target for novel therapeutic strategy against cancer.
Bjelogrlić SK, Srdić T, Radulović S. Bjelogrlić SK, et al. J BUON. 2006 Jul-Sep;11(3):267-76. J BUON. 2006. PMID: 17309148 Review. - Rapamycin: an anti-cancer immunosuppressant?
Law BK. Law BK. Crit Rev Oncol Hematol. 2005 Oct;56(1):47-60. doi: 10.1016/j.critrevonc.2004.09.009. Crit Rev Oncol Hematol. 2005. PMID: 16039868 Review.
Cited by
- Genetic determinants and potential therapeutic targets for pancreatic adenocarcinoma.
Reznik R, Hendifar AE, Tuli R. Reznik R, et al. Front Physiol. 2014 Mar 3;5:87. doi: 10.3389/fphys.2014.00087. eCollection 2014. Front Physiol. 2014. PMID: 24624093 Free PMC article. Review. - Expression of phosphorylated mTOR and its regulatory protein is related to biological behaviors of ameloblastoma.
Li N, Zhong M, Song M. Li N, et al. Int J Clin Exp Pathol. 2012;5(7):660-7. Epub 2012 Sep 5. Int J Clin Exp Pathol. 2012. PMID: 22977662 Free PMC article. - Inhibition of the mammalian target of rapamycin (mTOR) in advanced pancreatic cancer: results of two phase II studies.
Javle MM, Shroff RT, Xiong H, Varadhachary GA, Fogelman D, Reddy SA, Davis D, Zhang Y, Wolff RA, Abbruzzese JL. Javle MM, et al. BMC Cancer. 2010 Jul 14;10:368. doi: 10.1186/1471-2407-10-368. BMC Cancer. 2010. PMID: 20630061 Free PMC article. Clinical Trial. - Emerging therapies in pancreas cancer.
Kotowski A, Ma WW. Kotowski A, et al. J Gastrointest Oncol. 2011 Jun;2(2):93-103. doi: 10.3978/j.issn.2078-6891.2011.002. J Gastrointest Oncol. 2011. PMID: 22811835 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials
Miscellaneous