Matches in SemOpenAlex for { <https://semopenalex.org/work/W2741991702> ?p ?o ?g. }
- W2741991702 endingPage "3154" @default.
- W2741991702 startingPage "3138" @default.
- W2741991702 abstract "Activation of the telomere maintenance mechanism is a key hallmark of cancer. Human telomerase reverse transcriptase (hTERT) is the catalytic subunit of telomerase, which is highly expressed in more than 80% of tumors, including hepatocellular carcinoma (HCC). However, the exact mechanisms by which hTERT is up-regulated in HCCs and promotes tumor growth and progression is not fully understood. The aim of this study was to discover the novel molecular targets that modulate hTERT signaling and HCC growth. In this study, we pulled down and identified RBFOX3 (RNA binding protein fox-1 homolog 3) as a novel hTERT promoter-binding protein in HCC cells using biotin-streptavidin-agarose pull-down and proteomics approach, and validated it as a regulatory factor for hTERT signaling and tumor growth in HCCs. Knockdown of RBFOX3 suppressed the promoter activity and expression of hTERT and consequently inhibited the growth and progression of HCC cells in vitro and in vivo. The suppression of HCC growth mediated by RBFOX3 knockdown could be rescued by hTERT overexpression. Conversely, exogenous overexpression of RBFOX3 activated the promoter activity and expression of hTERT and promoted the growth and progression of HCC cells. Moreover, we found that RBFOX3 interacted with AP-2β to regulate the expression of hTERT. Furthermore, we demonstrated that RBFOX3 expression was higher in the tumor tissues of HCC patients compared to the corresponding paracancer tissues, and was positively correlated with hTERT expression. Kaplan-Meier analysis showed that the HCC patients with high levels of RBFOX3 and hTERT had poor prognosis. Collectively, our data indicate that RBFOX3 promotes HCC growth and progression and predicts a poor prognosis by activating the hTERT signaling, and suggest that the RBFOX3/hTERT pathway may be a potential therapeutic target for HCC patients." @default.
- W2741991702 created "2017-08-08" @default.
- W2741991702 creator A5005418531 @default.
- W2741991702 creator A5013852704 @default.
- W2741991702 creator A5017391031 @default.
- W2741991702 creator A5018202347 @default.
- W2741991702 creator A5020770785 @default.
- W2741991702 creator A5027887655 @default.
- W2741991702 creator A5028964644 @default.
- W2741991702 creator A5039896971 @default.
- W2741991702 creator A5042546997 @default.
- W2741991702 creator A5044522072 @default.
- W2741991702 creator A5046675610 @default.
- W2741991702 creator A5049368494 @default.
- W2741991702 creator A5060613630 @default.
- W2741991702 creator A5082321957 @default.
- W2741991702 creator A5083819054 @default.
- W2741991702 creator A5086519113 @default.
- W2741991702 creator A5089669072 @default.
- W2741991702 creator A5091798976 @default.
- W2741991702 date "2017-01-01" @default.
- W2741991702 modified "2023-10-16" @default.
- W2741991702 title "RBFOX3 Promotes Tumor Growth and Progression via hTERT Signaling and Predicts a Poor Prognosis in Hepatocellular Carcinoma" @default.
- W2741991702 cites W1835769532 @default.
- W2741991702 cites W1964457191 @default.
- W2741991702 cites W1968246267 @default.
- W2741991702 cites W1971669509 @default.
- W2741991702 cites W1983738311 @default.
- W2741991702 cites W1984374449 @default.
- W2741991702 cites W1998335196 @default.
- W2741991702 cites W2000971601 @default.
- W2741991702 cites W2002706824 @default.
- W2741991702 cites W2004561527 @default.
- W2741991702 cites W2010882280 @default.
- W2741991702 cites W2012201168 @default.
- W2741991702 cites W2016729072 @default.
- W2741991702 cites W2017752436 @default.
- W2741991702 cites W2021812738 @default.
- W2741991702 cites W2023645508 @default.
- W2741991702 cites W2036885380 @default.
- W2741991702 cites W2037516621 @default.
- W2741991702 cites W2039372333 @default.
- W2741991702 cites W2055353932 @default.
- W2741991702 cites W2055498826 @default.
- W2741991702 cites W2063625327 @default.
- W2741991702 cites W2067539793 @default.
- W2741991702 cites W2073954801 @default.
- W2741991702 cites W2108482850 @default.
- W2741991702 cites W2112891249 @default.
- W2741991702 cites W2124766044 @default.
- W2741991702 cites W2127443475 @default.
- W2741991702 cites W2143257102 @default.
- W2741991702 cites W2146703500 @default.
- W2741991702 cites W2149790687 @default.
- W2741991702 cites W2150262642 @default.
- W2741991702 cites W2150516960 @default.
- W2741991702 cites W2158496649 @default.
- W2741991702 cites W2162727919 @default.
- W2741991702 cites W2169733234 @default.
- W2741991702 cites W2171968985 @default.
- W2741991702 cites W2292767475 @default.
- W2741991702 cites W2338308550 @default.
- W2741991702 cites W2346196833 @default.
- W2741991702 cites W2397759082 @default.
- W2741991702 cites W2461398495 @default.
- W2741991702 cites W2474431374 @default.
- W2741991702 cites W2485286877 @default.
- W2741991702 cites W2507092954 @default.
- W2741991702 cites W2507603852 @default.
- W2741991702 cites W2514942338 @default.
- W2741991702 cites W2519523567 @default.
- W2741991702 cites W2563131589 @default.
- W2741991702 cites W2581259096 @default.
- W2741991702 cites W2917837889 @default.
- W2741991702 doi "https://doi.org/10.7150/thno.19506" @default.
- W2741991702 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5566111" @default.
- W2741991702 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28839469" @default.
- W2741991702 hasPublicationYear "2017" @default.
- W2741991702 type Work @default.
- W2741991702 sameAs 2741991702 @default.
- W2741991702 citedByCount "24" @default.
- W2741991702 countsByYear W27419917022018 @default.
- W2741991702 countsByYear W27419917022019 @default.
- W2741991702 countsByYear W27419917022020 @default.
- W2741991702 countsByYear W27419917022021 @default.
- W2741991702 countsByYear W27419917022022 @default.
- W2741991702 countsByYear W27419917022023 @default.
- W2741991702 crossrefType "journal-article" @default.
- W2741991702 hasAuthorship W2741991702A5005418531 @default.
- W2741991702 hasAuthorship W2741991702A5013852704 @default.
- W2741991702 hasAuthorship W2741991702A5017391031 @default.
- W2741991702 hasAuthorship W2741991702A5018202347 @default.
- W2741991702 hasAuthorship W2741991702A5020770785 @default.
- W2741991702 hasAuthorship W2741991702A5027887655 @default.
- W2741991702 hasAuthorship W2741991702A5028964644 @default.
- W2741991702 hasAuthorship W2741991702A5039896971 @default.
- W2741991702 hasAuthorship W2741991702A5042546997 @default.
- W2741991702 hasAuthorship W2741991702A5044522072 @default.