Matches in SemOpenAlex for { <https://semopenalex.org/work/W2143829302> ?p ?o ?g. }
- W2143829302 endingPage "1722" @default.
- W2143829302 startingPage "1713" @default.
- W2143829302 abstract "Obesity is rapidly becoming a pandemic and is associated with increased carcinogenesis. Obese populations have higher circulating levels of leptin in contrast to low concentrations of adiponectin. Hence, it is important to evaluate the dynamic role between adiponectin and leptin in obesity-related carcinogenesis. Recently, we reported the oncogenic role of leptin including its potential to increase tumor invasiveness and migration of hepatocellular carcinoma (HCC) cells. In the present study we investigated whether adiponectin could antagonize the oncogenic actions of leptin in HCC. We employed HCC cell lines HepG2 and Huh7, the nude mice-xenograft model of HCC, and immunohistochemistry data from tissue-microarray to demonstrate the antagonistic role of adiponectin on the oncogenic actions of leptin. Adiponectin treatment inhibited leptin-induced cell proliferation of HCC cells. Using scratch-migration and electric cell-substrate impedance-sensing-based migration assays, we found that adiponectin inhibited leptin-induced migration of HCC cells. Adiponectin treatment effectively blocked leptin-induced invasion of HCC cells in Matrigel invasion assays. Although leptin inhibited apoptosis in HCC cells, we found that adiponectin treatment induced apoptosis even in the presence of leptin. Analysis of the underlying molecular mechanisms revealed that adiponectin treatment reduced leptin-induced Stat3 and Akt phosphorylation. Adiponectin also increased suppressor of cytokine signaling (SOCS3), a physiologic negative regulator of leptin signal transduction. Importantly, adiponectin significantly reduced leptin-induced tumor burden in nude mice. In HCC samples, leptin expression significantly correlated with HCC proliferation as evaluated by Ki-67, whereas adiponectin expression correlated significantly with increased disease-free survival and inversely with tumor size and local recurrence. Conclusion: Collectively, these data demonstrate that adiponectin has the molecular potential to inhibit the oncogenic actions of leptin by blocking downstream effector molecules. (HEPATOLOGY 2010" @default.
- W2143829302 created "2016-06-24" @default.
- W2143829302 creator A5030200822 @default.
- W2143829302 creator A5035375857 @default.
- W2143829302 creator A5035543524 @default.
- W2143829302 creator A5049156516 @default.
- W2143829302 creator A5058989845 @default.
- W2143829302 creator A5059496981 @default.
- W2143829302 creator A5065427058 @default.
- W2143829302 creator A5070853337 @default.
- W2143829302 creator A5085828175 @default.
- W2143829302 creator A5088960523 @default.
- W2143829302 creator A5090861182 @default.
- W2143829302 date "2010-08-05" @default.
- W2143829302 modified "2023-09-26" @default.
- W2143829302 title "Adiponectin antagonizes the oncogenic actions of leptin in hepatocellular carcinogenesis" @default.
- W2143829302 cites W1524321743 @default.
- W2143829302 cites W1964814161 @default.
- W2143829302 cites W1971047979 @default.
- W2143829302 cites W1984061101 @default.
- W2143829302 cites W1997978122 @default.
- W2143829302 cites W2001727439 @default.
- W2143829302 cites W2011382710 @default.
- W2143829302 cites W2016298087 @default.
- W2143829302 cites W2029398685 @default.
- W2143829302 cites W2035528038 @default.
- W2143829302 cites W2040061273 @default.
- W2143829302 cites W2040856989 @default.
- W2143829302 cites W2041872947 @default.
- W2143829302 cites W2045599577 @default.
- W2143829302 cites W2045965545 @default.
- W2143829302 cites W2056972142 @default.
- W2143829302 cites W2058126433 @default.
- W2143829302 cites W2060503769 @default.
- W2143829302 cites W2065697164 @default.
- W2143829302 cites W2069224161 @default.
- W2143829302 cites W2070190142 @default.
- W2143829302 cites W2071875898 @default.
- W2143829302 cites W2078316187 @default.
- W2143829302 cites W2079146692 @default.
- W2143829302 cites W2091484442 @default.
- W2143829302 cites W2091759162 @default.
- W2143829302 cites W2095022880 @default.
- W2143829302 cites W2097055679 @default.
- W2143829302 cites W2107865201 @default.
- W2143829302 cites W2112182413 @default.
- W2143829302 cites W2117701806 @default.
- W2143829302 cites W2124588973 @default.
- W2143829302 cites W2137736712 @default.
- W2143829302 cites W2141662760 @default.
- W2143829302 cites W2147084771 @default.
- W2143829302 cites W2156503775 @default.
- W2143829302 cites W2162896364 @default.
- W2143829302 cites W2167596697 @default.
- W2143829302 cites W4205943196 @default.
- W2143829302 doi "https://doi.org/10.1002/hep.23892" @default.
- W2143829302 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2967627" @default.
- W2143829302 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20941777" @default.
- W2143829302 hasPublicationYear "2010" @default.
- W2143829302 type Work @default.
- W2143829302 sameAs 2143829302 @default.
- W2143829302 citedByCount "154" @default.
- W2143829302 countsByYear W21438293022012 @default.
- W2143829302 countsByYear W21438293022013 @default.
- W2143829302 countsByYear W21438293022014 @default.
- W2143829302 countsByYear W21438293022015 @default.
- W2143829302 countsByYear W21438293022016 @default.
- W2143829302 countsByYear W21438293022017 @default.
- W2143829302 countsByYear W21438293022018 @default.
- W2143829302 countsByYear W21438293022019 @default.
- W2143829302 countsByYear W21438293022020 @default.
- W2143829302 countsByYear W21438293022021 @default.
- W2143829302 countsByYear W21438293022022 @default.
- W2143829302 countsByYear W21438293022023 @default.
- W2143829302 crossrefType "journal-article" @default.
- W2143829302 hasAuthorship W2143829302A5030200822 @default.
- W2143829302 hasAuthorship W2143829302A5035375857 @default.
- W2143829302 hasAuthorship W2143829302A5035543524 @default.
- W2143829302 hasAuthorship W2143829302A5049156516 @default.
- W2143829302 hasAuthorship W2143829302A5058989845 @default.
- W2143829302 hasAuthorship W2143829302A5059496981 @default.
- W2143829302 hasAuthorship W2143829302A5065427058 @default.
- W2143829302 hasAuthorship W2143829302A5070853337 @default.
- W2143829302 hasAuthorship W2143829302A5085828175 @default.
- W2143829302 hasAuthorship W2143829302A5088960523 @default.
- W2143829302 hasAuthorship W2143829302A5090861182 @default.
- W2143829302 hasBestOaLocation W21438293021 @default.
- W2143829302 hasConcept C121608353 @default.
- W2143829302 hasConcept C126042315 @default.
- W2143829302 hasConcept C126322002 @default.
- W2143829302 hasConcept C134018914 @default.
- W2143829302 hasConcept C14372207 @default.
- W2143829302 hasConcept C171089720 @default.
- W2143829302 hasConcept C194832188 @default.
- W2143829302 hasConcept C2776782570 @default.
- W2143829302 hasConcept C2777391703 @default.
- W2143829302 hasConcept C2778923194 @default.
- W2143829302 hasConcept C2779306644 @default.