| Literature DB >> 32521727 |
Jisup Kim1, Joon-Yong Chung2, Young Soo Park1, Se Jin Jang1,3, Hyeong Ryul Kim4, Chang-Min Choi5,6, Joon Seon Song1.
Abstract
RIPK3 is a key regulator of necroptosis, which plays a double-edged sword role in tumor progression. CHIP is an E3 ubiquitin ligase that regulates necroptosis by degrading RIPK3. Here, we investigated the prognostic value of RIPK3 and CHIP expression in 404 patients with non-small cell lung cancer (NSCLC). Expressions of CHIP and RIPK3 showed opposite correlations with survival. CHIP expression was associated with the longer overall survival (OS), whereas RIPK3 expression was associated with the shorter OS. RIPK3 positivity showed marginal association with shorter OS and disease-free survival (DFS) in adjuvant radiotherapy recipients but not in non-recipients, suggesting that necroptosis may induce radioresistance. In multivariate analysis, CHIP expression was associated with longer OS. Compared with other patients, CHIP(-)/RIPK3(+) patients had shorter OS and DFS. In summary, in patients with NSCLC, the expression of CHIP was an independent favorable prognostic factor while that of RIPK3 was an adverse prognostic factor.Entities:
Keywords: carboxyl terminus of Hsp70-interacting protein (CHIP); necroptosis; non-small cell lung cancer; prognosis; receptor interacting serine/threonine kinase 3 (RIPK3)
Year: 2020 PMID: 32521727 DOI: 10.3390/cancers12061496
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639