| Literature DB >> 33230623 |
Blake A Jacobson1, Zeeshan Ahmad1, Sierra Chen2, Gabriella Waldusky1, Maxwell Dillenburg3, Emilia Stoian4, Daniel A Cambron5, Anil J Patel1, Manish R Patel1, Carston R Wagner3, Robert A Kratzke6,7.
Abstract
In order to suppress 5' cap-mediated translation a highly available inhibitor of the interaction between the 5' mRNA cap and the eIF4E complex has been developed. 4Ei-10 is a member of the class of ProTide compounds and has elevated membrane permeability and is a strong active chemical antagonist for eIF4E. Once taken up by cells it is converted by anchimeric activation of the lipophilic 2-(methylthio) ethyl protecting group and after that Hint1 P-N bond cleavage to N7-(p-chlorophenoxyethyl) guanosine 5'-monophosphate (7-Cl-Ph-Ethyl-GMP). Using this powerful interaction, it has been demonstrated that 4Ei-10 inhibits non-small cell lung cancer (NSCLC) cell growth. In addition, treatment of NSCLC cells with 4Ei-10 results in suppression of translation and diminished expression of a cohort of cellular proteins important to maintaining the malignant phenotype and resisting apoptosis such as Bcl-2, survivin, and ornithine decarboxylase (ODC). Finally, as a result of targeting the translation of anti-apoptotic proteins, NSCLC cells are synergized to be more sensitive to the existing anti-neoplastic treatment gemcitabine currently used in NSCLC therapy.Entities:
Keywords: 4Ei-10; Cap-dependent translation; Non-small cell lung cancer; ProTide; eIF4E; eIF4G
Mesh:
Substances:
Year: 2020 PMID: 33230623 DOI: 10.1007/s10637-020-01036-8
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850