| Literature DB >> 33658617 |
David Díaz-Carballo1, Sahitya Saka2, Ali H Acikelli2, Ekaterina Homp2, Julia Erwes2, Rebecca Demmig2, Jacqueline Klein2, Katrin Schröer2, Sascha Malak2, Flevy D'Souza2, Adrien Noa-Bolaño2, Saskia Menze2, Emilio Pano2, Swetlana Andrioff2, Marc Teipel2, Philip Dammann3, Diana Klein4, Amber Nasreen5, Andrea Tannapfel6, Nicole Grandi7, Enzo Tramontano7, Crista Ochsenfarth8, Dirk Strumberg2.
Abstract
In this work, we are reporting that "Shock and Kill", a therapeutic approach designed to eliminate latent HIV from cell reservoirs, is extrapolatable to cancer therapy. This is based on the observation that malignant cells express a spectrum of human endogenous retroviral elements (HERVs) which can be transcriptionally boosted by HDAC inhibitors. The endoretroviral gene HERV-V2 codes for an envelope protein, which resembles syncytins. It is significantly overexpressed upon exposure to HDAC inhibitors and can be effectively targeted by simultaneous application of TLR7/8 agonists, triggering intrinsic apoptosis. We demonstrated that this synergistic cytotoxic effect was accompanied by the functional disruption of the TLR7/8-NFκB, Akt/PKB, and Ras-MEK-ERK signalling pathways. CRISPR/Cas9 ablation of TLR7 and HERV-V1/V2 curtailed apoptosis significantly, proving the pivotal role of these elements in driving cell death. The effectiveness of this new approach was confirmed in ovarian tumour xenograft studies, revealing a promising avenue for future cancer therapies.Entities:
Year: 2021 PMID: 33658617 PMCID: PMC7930250 DOI: 10.1038/s42003-021-01800-3
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642