Nature, Journal Year: 2024, Volume and Issue: 629(8012), P. 543 - 554
Published: May 15, 2024
Language: Английский
Nature, Journal Year: 2024, Volume and Issue: 629(8012), P. 543 - 554
Published: May 15, 2024
Language: Английский
Cell, Journal Year: 2023, Volume and Issue: 186(8), P. 1564 - 1579
Published: April 1, 2023
Language: Английский
Citations
369Cancer Cell, Journal Year: 2023, Volume and Issue: 41(3), P. 421 - 433
Published: Feb. 16, 2023
Language: Английский
Citations
269Nature reviews. Cancer, Journal Year: 2022, Volume and Issue: 23(2), P. 95 - 111
Published: Dec. 9, 2022
Language: Английский
Citations
177Cell, Journal Year: 2023, Volume and Issue: 186(8), P. 1670 - 1688
Published: Feb. 28, 2023
Language: Английский
Citations
160Nature Cancer, Journal Year: 2023, Volume and Issue: 4(8), P. 1063 - 1082
Published: Aug. 3, 2023
Language: Английский
Citations
148Cell Metabolism, Journal Year: 2023, Volume and Issue: 35(8), P. 1283 - 1303
Published: Aug. 1, 2023
Language: Английский
Citations
96Nature Reviews Genetics, Journal Year: 2023, Volume and Issue: 24(9), P. 590 - 609
Published: May 11, 2023
Language: Английский
Citations
71Nature Communications, Journal Year: 2023, Volume and Issue: 14(1)
Published: Feb. 23, 2023
Abstract Serine synthesis is crucial for tumor growth and survival, but its regulatory mechanism in cancer remains elusive. Here, using integrative metabolomics transcriptomics analyses, we show a heterogeneity between metabolite transcript profiles. Specifically, the level of serine hepatocellular carcinoma (HCC) tissues increased, whereas expression phosphoglycerate dehydrogenase (PHGDH), first rate-limiting enzyme biosynthesis pathway, markedly downregulated. Interestingly, increased obtained by enhanced PHGDH catalytic activity due to protein arginine methyltransferase 1 (PRMT1)-mediated methylation at 236. PRMT1-mediated activation potentiates synthesis, ameliorates oxidative stress, promotes HCC vitro vivo. Furthermore, correlates with hyperactivation accumulation human tissues, predictive poor prognosis patients. Notably, blocking TAT-tagged nonmethylated peptide inhibits restrains an patient-derived xenograft (PDX) model subcutaneous cell-derived model. Overall, our findings reveal suggest as potential therapeutic vulnerability HCC.
Language: Английский
Citations
62Nature Metabolism, Journal Year: 2024, Volume and Issue: 6(1), P. 18 - 38
Published: Jan. 24, 2024
Language: Английский
Citations
59Signal Transduction and Targeted Therapy, Journal Year: 2024, Volume and Issue: 9(1)
Published: Aug. 5, 2024
Protein post-translational modification (PTM) is a covalent process that occurs in proteins during or after translation through the addition removal of one more functional groups, and has profound effect on protein function. Glycosylation most common PTMs, which polysaccharides are transferred to specific amino acid residues by glycosyltransferases. A growing body evidence suggests glycosylation essential for unfolding various activities organisms, such as playing key role regulation function, cell adhesion immune escape. Aberrant also closely associated with development diseases. Abnormal patterns linked emergence health conditions, including cancer, inflammation, autoimmune disorders, several other However, underlying composition structure glycosylated have not been determined. It imperative fully understand internal differential expression glycosylation, incorporate advanced detection technologies keep knowledge advancing. Investigations clinical applications focused sensitive promising biomarkers, effective small molecule targeted drugs emerging vaccines. These studies provide new area novel therapeutic strategies based glycosylation.
Language: Английский
Citations
38