| Literature DB >> 31559416 |
Huan Fang1,2,3, Guangshi Du3, Qiuju Wu3, Rong Liu3, Ceshi Chen3, Jing Feng2,4,5.
Abstract
Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer with poor clinical outcomes and without effective targeted therapies. Numerous studies have suggested that HDAC inhibitors (TSA/SAHA) may be effective in TNBCs. Proline oxidase, also known as proline dehydrogenase (POX/PRODH), is a key enzyme in the proline metabolism pathway and plays a vital role in tumorigenesis. In this study, we found that HDAC inhibitors (TSA/SAHA) significantly increased POX expression and autophagy through activating AMPK. Depletion of POX decreased autophagy and increased apoptosis induced by HDAC inhibitors in TNBC cells. These results suggest that POX contributes to cell survival under chemotherapeutic stresses and might serve as a potential target for treatment of TNBC. © Crown copyright 2019.Entities:
Keywords: AMPK; HDAC inhibitors; POX; apoptosis; autophagy; triple-negative breast cancer
Year: 2019 PMID: 31559416 DOI: 10.1093/abbs/gmz097
Source DB: PubMed Journal: Acta Biochim Biophys Sin (Shanghai) ISSN: 1672-9145 Impact factor: 3.848