| Literature DB >> 28401179 |
Timothy J Bergmann1, Fiorenza Fumagalli2, Marisa Loi1, Maurizio Molinari3.
Abstract
Amplification of the candidate oncogene TLOC1/SEC62 in tumors correlates with reduced patient survival. The recently reported role of SEC62 as an autophagy receptor that controls endoplasmic reticulum (ER) size and function might open new scenarios for understanding the phenotypes and treat SEC62high tumors, which are characterized by high ER stress tolerance.Entities:
Keywords: Autophagy receptor; ER-phagy; LIR; SEC62; TLOC1; cancer; endoplasmic reticulum; oncogene; recovER-phagy; selective autophagy; tumor
Year: 2017 PMID: 28401179 PMCID: PMC5383369 DOI: 10.1080/23723556.2016.1264351
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556