نمایش مختصر رکورد

dc.date.accessioned1399-07-08T18:08:56Zfa_IR
dc.date.accessioned2020-09-29T18:08:56Z
dc.date.available1399-07-08T18:08:56Zfa_IR
dc.date.available2020-09-29T18:08:56Z
dc.date.issued2013-08-01en_US
dc.date.issued1392-05-10fa_IR
dc.identifier.citation(2013). Effects of Vinorelbine on Cisplatin Resistance Reversal in Human Lung Cancer A549/DDP Cells. Asian Pacific Journal of Cancer Prevention, 14(8), 4635-4639.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_28003.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/37331
dc.description.abstractMulti-drug resistance (MDR) is an essential aspect of human lung cancer chemotherapy failure. Recentstudies have shown that vinorelbine is involved in underlying processes in human tumors, reversing the MDRinseveral types of cancer cells. However, the roles and potential mechanism are not fully clear. In this study,we explored effects of vinorelbine in multi-drug resistance reversal of human lung cancer A549/DDP cells. Wefound that vinorelbine increased drug sensitivity to cisplatin and intracellular accumulation of rhodamine-123,while decreasing expression of P-glycoprotein (P-gp), multi-drug resistance-associated protein (MRP1) andglutathione-S-transferase π (GST-π) in A549/DDP cells. At the same time, we also established downregulationof p-Akt and decreased transcriptional activation of NF-κB and twist after vinorelbine treatment. The resultsindicated that vinorelbine might be used as a potential therapeutic strategy in human lung cancer.en_US
dc.format.extent749
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.subjectvinorelbineen_US
dc.subjecthuman lung canceren_US
dc.subjectMultidrug Resistanceen_US
dc.titleEffects of Vinorelbine on Cisplatin Resistance Reversal in Human Lung Cancer A549/DDP Cellsen_US
dc.typeTexten_US
dc.citation.volume14
dc.citation.issue8
dc.citation.spage4635
dc.citation.epage4639


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