https://scholars.lib.ntu.edu.tw/handle/123456789/390100
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | SHING-HWA LIU | en |
dc.creator | Su, C.-C.;Liu, S.-H.;Lee, K.-I.;Huang, K.-T.;Lu, T.-H.;Fang, K.-M.;Wu, C.-C.;Yen, C.-C.;Lai, C.-H.;Su, Y.-C.;Huang, C.-F. | - |
dc.date.accessioned | 2018-09-10T15:17:33Z | - |
dc.date.available | 2018-09-10T15:17:33Z | - |
dc.date.issued | 2015 | - |
dc.identifier.uri | http://www.scopus.com/inward/record.url?eid=2-s2.0-84929149437&partnerID=MN8TOARS | - |
dc.identifier.uri | http://scholars.lib.ntu.edu.tw/handle/123456789/390100 | - |
dc.description.abstract | Bladder cancer is a common malignancy worldwide. However, there is still no effective therapy for bladder cancer. In this study, we investigated the cytotoxic effects of cantharidin [a natural toxin produced (pure compound) from Chinese blister beetles (Mylabrisphalerata or Mylabriscichorii) and Spanish flies (Cantharis vesicatoria)] in human bladder cancer cell lines (including: T24 and RT4 cells). Treatment of human bladder cancer cells with cantharidin significantly decreased cell viability. The increase in the expressions of caspase-3 activity and cleaved form of caspase-9/-7/-3 were also increased in cantharidin-treated T24 cells. Furthermore, cantharidin increased the levels of phospho-eIF2α and Grp78 and decreased the protein expression of procaspase-12, which was accompanied by the increase in calpain activity in T24 cells. Cantharidin was capable of increasing the intracellular Ca2+ and the phosphorylation of protein kinase C (PKC) in T24 cells. The addition of BAPTA/AM (a Ca2+ chelator) and RO320432 (a selective cell-permeable PKC inhibitor) effectively reversed the increase in caspase-3 and calpain activity, the phosphorylation levels of PKC and eIF2α and Grp78 protein expression, and the decrease in procaspase-12 expression induced by cantharidin. Importantly, cantharidin significantly decreased the tumor volume (a dramatic 71% reduction after 21 days of treatment) in nude mice xenografted with T24 cells. Taken together, these results indicate cantharidin induced human bladder cancer cell apoptosis through a calcium/PKC-regulated ER stress pathway. These findings suggest that cantharidin may be a novel and potential anticancer agent targeting on bladder cancer cells. ? 2015 World Scientific Publishing Company & Institute for Advanced Research in Asian Science and Medicine. | - |
dc.language | en | en |
dc.relation.ispartof | American Journal of Chinese Medicine | en_US |
dc.source | AH | - |
dc.subject | Bladder Cancer Cells; Calcium; Cantharidin; ER Stress; PKC | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | calcium; calpain; cantharidin; caspase; caspase 12; caspase 3; caspase 7; caspase 9; glucose regulated protein 78; initiation factor 2alpha; procaspase 12; protein kinase C; unclassified drug; antineoplastic agent; calcium; cantharidin; caspase 3; protein kinase C; animal experiment; animal model; antineoplastic activity; apoptosis; Article; beetle; bladder cancer; bladder cancer cell line; calcium cell level; cancer cell; cancer therapy; Cantharis vesicatoria; cell viability; Diptera; drug cytotoxicity; endoplasmic reticulum stress; enzyme activity; enzyme linked immunosorbent assay; enzyme phosphorylation; human; human cell; male; mouse; MTT assay; Mylabriscichorii; Mylabrisphalerata; nonhuman; protein expression; protein phosphorylation; regulatory mechanism; therapy effect; tumor volume; tumor xenograft; Western blotting; animal; apoptosis; Bagg albino mouse; bladder tumor; drug effects; endoplasmic reticulum stress; genetics; metabolism; nude mouse; papilloma; pathology; physiology; signal transduction; tumor cell line; upregulation; Animals; Antineoplastic Agents; Apoptosis; Calcium; Cantharidin; Caspase 3; Cell Line, Tumor; Endoplasmic Reticulum Stress; Humans; Male; Mice, Inbred BALB C; Mice, Nude; Papilloma; Protein Kinase C; Signal Transduction; Up-Regulation; Urinary Bladder Neoplasms | - |
dc.title | Cantharidin induces apoptosis through the calcium/PKC-regulated endoplasmic reticulum stress pathway in human bladder cancer cells | - |
dc.type | journal article | en |
dc.identifier.doi | 10.1142/S0192415X15500366 | - |
dc.relation.pages | 581-600 | - |
dc.relation.journalvolume | 43 | - |
dc.relation.journalissue | 3 | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.openairetype | journal article | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
item.fulltext | no fulltext | - |
crisitem.author.dept | Toxicology | - |
crisitem.author.orcid | 0000-0002-9976-1197 | - |
crisitem.author.parentorg | College of Medicine | - |
顯示於: | 毒理學研究所 |
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