Matches in SemOpenAlex for { <https://semopenalex.org/work/W2537750806> ?p ?o ?g. }
- W2537750806 endingPage "4392" @default.
- W2537750806 startingPage "4385" @default.
- W2537750806 abstract "Hepatocellular carcinoma (HCC), which is a type of malignant tumor, is the fifth most common cancer in men and ninth in women worldwide. The aim of the present study was to investigate the antitumor effect of diosmetin (DIOS) in hepatocellular carcinoma HepG2 cells. The proliferation, apoptosis and autophagy rates of HepG2 cells were measured following treatment with DIOS. The effects of DIOS treatment on HepG2 cell proliferation and apoptosis rates were analyzed using MTT assays and Annexin V staining, respectively. The effect of DIOS treatment on autophagy levels was assessed using transmission electron microscopy, green fluorescent protein (GFP)‑microtubule‑associated protein 1 light chain (LC3) transfection and LysoTracker Red staining. Furthermore, bafilomycin A1 (BA1), an autophagy inhibitor, was used to assess the association between DIOS and cell autophagy, proliferation and apoptosis. In addition, the expression of autophagy‑related proteins [mammalian target of rapamycin (mTOR), phosphatidylinositol 3‑kinase, P70S6K, phosphoinositide‑dependent kinase‑1, extracellular signal‑regulated kinase, 5'‑AMP‑activated protein kinase and Akt] and apoptosis‑related proteins [B‑cell lymphoma (Bcl)‑2‑associated X protein, Bak, p53, Bcl‑2 and caspase‑3] were analyzed by western blotting. The results revealed that DIOS significantly inhibited proliferation (P<0.01) and induced apoptosis (P<0.001) in HepG2 cells. It was also demonstrated that DIOS triggered autophagy by regulating the mTOR pathway in HepG2 cells. Notably, following treatment of HepG2 cells with the autophagy inhibitor, BA1, the expression of apoptosis‑related proteins, including Bax, Bak and p53, were significantly decreased (P<0.05), and cell viability was recovered to a certain extent. In conclusion, DIOS inhibits cell proliferation and induces apoptosis in HepG2 cells via regulation of the mTOR pathway. Thus, the results of the current study indicate that DIOS may present a potential therapeutic agent for HCC treatment." @default.
- W2537750806 created "2016-10-28" @default.
- W2537750806 creator A5028294527 @default.
- W2537750806 creator A5034180607 @default.
- W2537750806 creator A5040082411 @default.
- W2537750806 creator A5048826252 @default.
- W2537750806 creator A5067819286 @default.
- W2537750806 creator A5085352453 @default.
- W2537750806 date "2016-10-19" @default.
- W2537750806 modified "2023-10-16" @default.
- W2537750806 title "Diosmetin inhibits cell proliferation and induces apoptosis by regulating autophagy via the mammalian target of rapamycin pathway in hepatocellular carcinoma HepG2 cells" @default.
- W2537750806 cites W1482463156 @default.
- W2537750806 cites W1757407923 @default.
- W2537750806 cites W1964554985 @default.
- W2537750806 cites W1970206154 @default.
- W2537750806 cites W1972336737 @default.
- W2537750806 cites W1975856746 @default.
- W2537750806 cites W1976370980 @default.
- W2537750806 cites W1985561691 @default.
- W2537750806 cites W1986522336 @default.
- W2537750806 cites W1991398927 @default.
- W2537750806 cites W1994796945 @default.
- W2537750806 cites W1996499700 @default.
- W2537750806 cites W1998334997 @default.
- W2537750806 cites W2002828077 @default.
- W2537750806 cites W2017479911 @default.
- W2537750806 cites W2022564524 @default.
- W2537750806 cites W2030798063 @default.
- W2537750806 cites W2034866136 @default.
- W2537750806 cites W2038405639 @default.
- W2537750806 cites W2041657200 @default.
- W2537750806 cites W2051252157 @default.
- W2537750806 cites W2056036444 @default.
- W2537750806 cites W2060646928 @default.
- W2537750806 cites W2063033676 @default.
- W2537750806 cites W2066335867 @default.
- W2537750806 cites W2068153705 @default.
- W2537750806 cites W2068611573 @default.
- W2537750806 cites W2073947345 @default.
- W2537750806 cites W2079351077 @default.
- W2537750806 cites W2101220947 @default.
- W2537750806 cites W2104462720 @default.
- W2537750806 cites W2107616615 @default.
- W2537750806 cites W2113263985 @default.
- W2537750806 cites W2117692326 @default.
- W2537750806 cites W2124520342 @default.
- W2537750806 cites W2138780264 @default.
- W2537750806 cites W2141976464 @default.
- W2537750806 cites W2145434871 @default.
- W2537750806 cites W2146181702 @default.
- W2537750806 cites W2148047158 @default.
- W2537750806 cites W2149388384 @default.
- W2537750806 cites W2150320868 @default.
- W2537750806 cites W2163827556 @default.
- W2537750806 cites W2166895841 @default.
- W2537750806 cites W2171575676 @default.
- W2537750806 cites W2210083505 @default.
- W2537750806 cites W2330192046 @default.
- W2537750806 cites W2402001738 @default.
- W2537750806 doi "https://doi.org/10.3892/ol.2016.5301" @default.
- W2537750806 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5228182" @default.
- W2537750806 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28101201" @default.
- W2537750806 hasPublicationYear "2016" @default.
- W2537750806 type Work @default.
- W2537750806 sameAs 2537750806 @default.
- W2537750806 citedByCount "21" @default.
- W2537750806 countsByYear W25377508062017 @default.
- W2537750806 countsByYear W25377508062018 @default.
- W2537750806 countsByYear W25377508062019 @default.
- W2537750806 countsByYear W25377508062020 @default.
- W2537750806 countsByYear W25377508062021 @default.
- W2537750806 countsByYear W25377508062022 @default.
- W2537750806 countsByYear W25377508062023 @default.
- W2537750806 crossrefType "journal-article" @default.
- W2537750806 hasAuthorship W2537750806A5028294527 @default.
- W2537750806 hasAuthorship W2537750806A5034180607 @default.
- W2537750806 hasAuthorship W2537750806A5040082411 @default.
- W2537750806 hasAuthorship W2537750806A5048826252 @default.
- W2537750806 hasAuthorship W2537750806A5067819286 @default.
- W2537750806 hasAuthorship W2537750806A5085352453 @default.
- W2537750806 hasBestOaLocation W25377508061 @default.
- W2537750806 hasConcept C153911025 @default.
- W2537750806 hasConcept C184235292 @default.
- W2537750806 hasConcept C190283241 @default.
- W2537750806 hasConcept C203522944 @default.
- W2537750806 hasConcept C29537977 @default.
- W2537750806 hasConcept C502942594 @default.
- W2537750806 hasConcept C53227056 @default.
- W2537750806 hasConcept C55493867 @default.
- W2537750806 hasConcept C62112901 @default.
- W2537750806 hasConcept C62478195 @default.
- W2537750806 hasConcept C75217442 @default.
- W2537750806 hasConcept C86554907 @default.
- W2537750806 hasConcept C86803240 @default.
- W2537750806 hasConcept C88634738 @default.
- W2537750806 hasConcept C95444343 @default.
- W2537750806 hasConceptScore W2537750806C153911025 @default.
- W2537750806 hasConceptScore W2537750806C184235292 @default.