Matches in SemOpenAlex for { <https://semopenalex.org/work/W1857236668> ?p ?o ?g. }
- W1857236668 endingPage "4678" @default.
- W1857236668 startingPage "4665" @default.
- W1857236668 abstract "Esculetin (6,7-dihydroxycoumarin), a derivative of coumarin compound, is found in traditional medicinal herbs. It has been shown that esculetin triggers diverse cellular signal transduction pathways leading to regulation of physiology in different models. However, whether esculetin affects Ca2+ homeostasis in breast cancer cells has not been explored. This study examined the underlying mechanism of cytotoxicity induced by esculetin and established the relationship between Ca2+ signaling and cytotoxicity in human breast cancer cells. The results showed that esculetin induced concentration-dependent rises in the intracellular Ca2+ concentration ([Ca2+]i) in ZR-75-1 (but not in MCF-7 and MDA-MB-231) human breast cancer cells. In ZR-75-1 cells, this Ca2+ signal response was reduced by removing extracellular Ca2+ and was inhibited by the store-operated Ca2+ channel blocker 2-aminoethoxydiphenyl borate (2-APB). In Ca2+-free medium, pre-treatment with the endoplasmic reticulum Ca2+ pump inhibitor thapsigargin (TG) abolished esculetin-induced [Ca2+]i rises. Conversely, incubation with esculetin abolished TG-induced [Ca2+]i rises. Esculetin induced cytotoxicity that involved apoptosis, as supported by the reduction of mitochondrial membrane potential and the release of cytochrome c and the proteolytic activation of caspase-9/caspase-3, which were partially reversed by pre-chelating cytosolic Ca2+ with 1,2-bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid-acetoxymethyl ester (BAPTA-AM). Moreover, esculetin increased the percentage of cells in G2/M phase and regulated the expressions of p53, p21, CDK1, and cyclin B1. Together, in ZR-75-1 cells, esculetin induced [Ca2+]i rises by releasing Ca2+ from the ER and causing Ca2+ influx through 2-APB-sensitive store-operated Ca2+ entry. Furthermore, esculetin activated Ca2+-associated mitochondrial apoptotic pathways that involved G2/M cell cycle arrest." @default.
- W1857236668 created "2016-06-24" @default.
- W1857236668 creator A5006321114 @default.
- W1857236668 creator A5008213717 @default.
- W1857236668 creator A5018962870 @default.
- W1857236668 creator A5039254218 @default.
- W1857236668 creator A5054056894 @default.
- W1857236668 creator A5084071892 @default.
- W1857236668 creator A5087637496 @default.
- W1857236668 date "2015-10-28" @default.
- W1857236668 modified "2023-10-16" @default.
- W1857236668 title "Esculetin, a natural coumarin compound, evokes Ca2+ movement and activation of Ca2+-associated mitochondrial apoptotic pathways that involved cell cycle arrest in ZR-75-1 human breast cancer cells" @default.
- W1857236668 cites W1271389891 @default.
- W1857236668 cites W1550247880 @default.
- W1857236668 cites W1556575182 @default.
- W1857236668 cites W1951756999 @default.
- W1857236668 cites W1964720050 @default.
- W1857236668 cites W1974980101 @default.
- W1857236668 cites W1976300340 @default.
- W1857236668 cites W1979129905 @default.
- W1857236668 cites W1989089243 @default.
- W1857236668 cites W1996024251 @default.
- W1857236668 cites W2006259612 @default.
- W1857236668 cites W2010756788 @default.
- W1857236668 cites W2010896133 @default.
- W1857236668 cites W2015571368 @default.
- W1857236668 cites W2016492849 @default.
- W1857236668 cites W2016933408 @default.
- W1857236668 cites W2019961716 @default.
- W1857236668 cites W2020462357 @default.
- W1857236668 cites W2020945121 @default.
- W1857236668 cites W2022015605 @default.
- W1857236668 cites W2030913204 @default.
- W1857236668 cites W2036145275 @default.
- W1857236668 cites W2036752555 @default.
- W1857236668 cites W2037536286 @default.
- W1857236668 cites W2041383551 @default.
- W1857236668 cites W2043841869 @default.
- W1857236668 cites W2050350780 @default.
- W1857236668 cites W2050805381 @default.
- W1857236668 cites W2053827285 @default.
- W1857236668 cites W2055206436 @default.
- W1857236668 cites W2058449890 @default.
- W1857236668 cites W2063854658 @default.
- W1857236668 cites W2064719918 @default.
- W1857236668 cites W2068728258 @default.
- W1857236668 cites W2069982086 @default.
- W1857236668 cites W2070164781 @default.
- W1857236668 cites W2070832223 @default.
- W1857236668 cites W2077415389 @default.
- W1857236668 cites W2086802798 @default.
- W1857236668 cites W2089218510 @default.
- W1857236668 cites W2095458284 @default.
- W1857236668 cites W2110376527 @default.
- W1857236668 cites W2111278167 @default.
- W1857236668 cites W2124034869 @default.
- W1857236668 cites W2127594071 @default.
- W1857236668 cites W2127714324 @default.
- W1857236668 cites W2130866079 @default.
- W1857236668 cites W2137258759 @default.
- W1857236668 cites W2141260882 @default.
- W1857236668 cites W2143654194 @default.
- W1857236668 cites W2152385225 @default.
- W1857236668 cites W2161163021 @default.
- W1857236668 cites W2168457230 @default.
- W1857236668 cites W2169238639 @default.
- W1857236668 cites W2329075564 @default.
- W1857236668 cites W2397578201 @default.
- W1857236668 cites W2407651294 @default.
- W1857236668 cites W2437247476 @default.
- W1857236668 cites W4210298392 @default.
- W1857236668 cites W4249424055 @default.
- W1857236668 cites W4255760236 @default.
- W1857236668 cites W65197630 @default.
- W1857236668 cites W2283244067 @default.
- W1857236668 doi "https://doi.org/10.1007/s13277-015-4286-1" @default.
- W1857236668 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26508031" @default.
- W1857236668 hasPublicationYear "2015" @default.
- W1857236668 type Work @default.
- W1857236668 sameAs 1857236668 @default.
- W1857236668 citedByCount "21" @default.
- W1857236668 countsByYear W18572366682016 @default.
- W1857236668 countsByYear W18572366682017 @default.
- W1857236668 countsByYear W18572366682018 @default.
- W1857236668 countsByYear W18572366682019 @default.
- W1857236668 countsByYear W18572366682021 @default.
- W1857236668 countsByYear W18572366682022 @default.
- W1857236668 countsByYear W18572366682023 @default.
- W1857236668 crossrefType "journal-article" @default.
- W1857236668 hasAuthorship W1857236668A5006321114 @default.
- W1857236668 hasAuthorship W1857236668A5008213717 @default.
- W1857236668 hasAuthorship W1857236668A5018962870 @default.
- W1857236668 hasAuthorship W1857236668A5039254218 @default.
- W1857236668 hasAuthorship W1857236668A5054056894 @default.
- W1857236668 hasAuthorship W1857236668A5084071892 @default.
- W1857236668 hasAuthorship W1857236668A5087637496 @default.
- W1857236668 hasConcept C109316439 @default.
- W1857236668 hasConcept C121608353 @default.