| Literature DB >> 27614414 |
Roopa Rai1, Monali Banerjee2, Darren H Wong3, Emma McCullagh1, Ashu Gupta4, Shailendra Tripathi4, Eduardo Riquelme5, Ramnivas Jangir4, Shyamraj Yadav4, Mohd Raja4, Pankaj Melkani4, Vikas Dixit4, Umesh Patil4, Ritesh Shrivastava2, Sandip Middya2, Felipe Olivares5, Javier Guerrero5, Arjun Surya2, Son M Pham1, Sebastián Bernales1, Andrew A Protter1, David T Hung1, Sarvajit Chakravarty1.
Abstract
Temozolomide is a chemotherapeutic agent that is used in the treatment of glioblastoma and other malignant gliomas. It acts through DNA alkylation, but treatment is limited by its systemic toxicity and neutralization of DNA alkylation by upregulation of the O6-methylguanine-DNA methyltransferase gene. Both of these limiting factors can be addressed by achieving higher concentrations of TMZ in the brain. Our research has led to the discovery of new analogs of temozolomide with improved brain:plasma ratios when dosed in vivo in rats. These compounds are imidazotetrazine analogs, expected to act through the same mechanism as temozolomide. With reduced systemic exposure, these new agents have the potential to improve efficacy and therapeutic index in the treatment of glioblastoma.Entities:
Keywords: Chemotheraphy; Glioblastoma; O(6)-Methyl-2′-deoxyguanosine (O(6)-MedG); Temozolomide
Mesh:
Substances:
Year: 2016 PMID: 27614414 DOI: 10.1016/j.bmcl.2016.08.064
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823