Matches in SemOpenAlex for { <https://semopenalex.org/work/W3138703087> ?p ?o ?g. }
- W3138703087 endingPage "2435" @default.
- W3138703087 startingPage "2421" @default.
- W3138703087 abstract "Colorectal cancer (CRC) is the third leading cause of cancer-related deaths in the US. Understanding the mechanisms of CRC progression is essential to improve treatment. Mitochondria is the powerhouse for healthy cells. However, in tumor cells, less energy is produced by the mitochondria and metabolic reprogramming is an early hallmark of cancer. The metabolic differences between normal and cancer cells are being interrogated to uncover new therapeutic approaches. Mitochondria targeting PTEN-induced kinase 1 (PINK1) is a key regulator of mitophagy, the selective elimination of damaged mitochondria by autophagy. Defective mitophagy is increasingly associated with various diseases including CRC. However, a significant gap exists in our understanding of how PINK1-dependent mitophagy participates in the metabolic regulation of CRC. By mining Oncomine, we found that PINK1 expression was downregulated in human CRC tissues compared to normal colons. Moreover, disruption of PINK1 increased colon tumorigenesis in two colitis-associated CRC mouse models, suggesting that PINK1 functions as a tumor suppressor in CRC. PINK1 overexpression in murine colon tumor cells promoted mitophagy, decreased glycolysis and increased mitochondrial respiration potentially via activation of p53 signaling pathways. In contrast, PINK1 deletion decreased apoptosis, increased glycolysis, and reduced mitochondrial respiration and p53 signaling. Interestingly, PINK1 overexpression in vivo increased apoptotic cell death and suppressed colon tumor xenograft growth. Metabolomic analysis revealed that acetyl-CoA was significantly reduced in tumors with PINK1 overexpression, which was partly due to activation of the HIF-1α-pyruvate dehydrogenase (PDH) kinase 1 (PDHK1)-PDHE1α axis. Strikingly, treating mice with acetate increased acetyl-CoA levels and rescued PINK1-suppressed tumor growth. Importantly, PINK1 disruption simultaneously increased xenografted tumor growth and acetyl-CoA production. In conclusion, mitophagy protein PINK1 suppresses colon tumor growth by metabolic reprogramming and reducing acetyl-CoA production." @default.
- W3138703087 created "2021-03-29" @default.
- W3138703087 creator A5007631869 @default.
- W3138703087 creator A5012353087 @default.
- W3138703087 creator A5020176677 @default.
- W3138703087 creator A5021651278 @default.
- W3138703087 creator A5021823990 @default.
- W3138703087 creator A5049598610 @default.
- W3138703087 creator A5081348222 @default.
- W3138703087 creator A5088690019 @default.
- W3138703087 date "2021-03-15" @default.
- W3138703087 modified "2023-10-11" @default.
- W3138703087 title "Mitophagy protein PINK1 suppresses colon tumor growth by metabolic reprogramming via p53 activation and reducing acetyl-CoA production" @default.
- W3138703087 cites W1528644208 @default.
- W3138703087 cites W1972254548 @default.
- W3138703087 cites W1977622464 @default.
- W3138703087 cites W1977918192 @default.
- W3138703087 cites W1998976350 @default.
- W3138703087 cites W1999034430 @default.
- W3138703087 cites W2005833897 @default.
- W3138703087 cites W2026778985 @default.
- W3138703087 cites W2028114269 @default.
- W3138703087 cites W2033958147 @default.
- W3138703087 cites W2044515618 @default.
- W3138703087 cites W2047883857 @default.
- W3138703087 cites W2052543023 @default.
- W3138703087 cites W2062344929 @default.
- W3138703087 cites W2062515127 @default.
- W3138703087 cites W2063186159 @default.
- W3138703087 cites W2077669333 @default.
- W3138703087 cites W2078770291 @default.
- W3138703087 cites W2092699248 @default.
- W3138703087 cites W2093677429 @default.
- W3138703087 cites W2113707020 @default.
- W3138703087 cites W2118351194 @default.
- W3138703087 cites W2119239003 @default.
- W3138703087 cites W2126133274 @default.
- W3138703087 cites W2150027419 @default.
- W3138703087 cites W2154887758 @default.
- W3138703087 cites W2157099092 @default.
- W3138703087 cites W2160427027 @default.
- W3138703087 cites W2223535266 @default.
- W3138703087 cites W2253959633 @default.
- W3138703087 cites W2467807723 @default.
- W3138703087 cites W2508132062 @default.
- W3138703087 cites W2527719044 @default.
- W3138703087 cites W2537547167 @default.
- W3138703087 cites W2551880155 @default.
- W3138703087 cites W2567473117 @default.
- W3138703087 cites W2584861860 @default.
- W3138703087 cites W2602035017 @default.
- W3138703087 cites W2726754850 @default.
- W3138703087 cites W2749296525 @default.
- W3138703087 cites W2761556050 @default.
- W3138703087 cites W2765107560 @default.
- W3138703087 cites W2801261091 @default.
- W3138703087 cites W2809281987 @default.
- W3138703087 cites W2886011114 @default.
- W3138703087 cites W2887997888 @default.
- W3138703087 cites W2919328337 @default.
- W3138703087 cites W2943104900 @default.
- W3138703087 cites W2967801303 @default.
- W3138703087 cites W2976495952 @default.
- W3138703087 cites W2987264421 @default.
- W3138703087 cites W2991610197 @default.
- W3138703087 cites W2999417355 @default.
- W3138703087 doi "https://doi.org/10.1038/s41418-021-00760-9" @default.
- W3138703087 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8329176" @default.
- W3138703087 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33723373" @default.
- W3138703087 hasPublicationYear "2021" @default.
- W3138703087 type Work @default.
- W3138703087 sameAs 3138703087 @default.
- W3138703087 citedByCount "43" @default.
- W3138703087 countsByYear W31387030872021 @default.
- W3138703087 countsByYear W31387030872022 @default.
- W3138703087 countsByYear W31387030872023 @default.
- W3138703087 crossrefType "journal-article" @default.
- W3138703087 hasAuthorship W3138703087A5007631869 @default.
- W3138703087 hasAuthorship W3138703087A5012353087 @default.
- W3138703087 hasAuthorship W3138703087A5020176677 @default.
- W3138703087 hasAuthorship W3138703087A5021651278 @default.
- W3138703087 hasAuthorship W3138703087A5021823990 @default.
- W3138703087 hasAuthorship W3138703087A5049598610 @default.
- W3138703087 hasAuthorship W3138703087A5081348222 @default.
- W3138703087 hasAuthorship W3138703087A5088690019 @default.
- W3138703087 hasBestOaLocation W31387030871 @default.
- W3138703087 hasConcept C121608353 @default.
- W3138703087 hasConcept C126322002 @default.
- W3138703087 hasConcept C184235292 @default.
- W3138703087 hasConcept C185592680 @default.
- W3138703087 hasConcept C190283241 @default.
- W3138703087 hasConcept C20251656 @default.
- W3138703087 hasConcept C203522944 @default.
- W3138703087 hasConcept C2776804853 @default.
- W3138703087 hasConcept C2777668072 @default.
- W3138703087 hasConcept C2779134260 @default.
- W3138703087 hasConcept C2779324830 @default.
- W3138703087 hasConcept C2779734285 @default.