Gambogic acid sensitizes breast cancer cells to TRAIL-induced apoptosis by promoting the crosstalk of extrinsic and intrinsic apoptotic signalings

التفاصيل البيبلوغرافية
العنوان: Gambogic acid sensitizes breast cancer cells to TRAIL-induced apoptosis by promoting the crosstalk of extrinsic and intrinsic apoptotic signalings
المؤلفون: Peng Li, Xu Wu, Anqi Wang, Shengpeng Wang, Chenyu Sun, Zhangfeng Zhong, Chenyang Li, Hongxun Tao, Yingqi Xu, Yitao Wang
المصدر: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 119
سنة النشر: 2017
مصطلحات موضوعية: 0301 basic medicine, Agonist, medicine.drug_class, Xanthones, Apoptosis, Breast Neoplasms, Toxicology, TNF-Related Apoptosis-Inducing Ligand, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Breast cancer, Cell Line, Tumor, medicine, Humans, biology, General Medicine, medicine.disease, biology.organism_classification, Mitochondria, Enzyme Activation, Crosstalk (biology), 030104 developmental biology, chemistry, Garcinia hanburyi, Drug Resistance, Neoplasm, 030220 oncology & carcinogenesis, Caspases, Cancer cell, Cancer research, Gambogic acid, Tumor necrosis factor alpha, Female, Food Science, Signal Transduction
الوصف: Due to the ability of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) to induce cancer cell apoptosis selectively, TRAIL has attracted significant interest in the treatment of cancer. However, although TRAIL triggers apoptosis in a broad range of cancer cells, most primary cancers are often intrinsically TRAIL-resistant, or can acquire resistance after TRAIL treatment, evocating new strategies to overcome TRAIL resistance. Gambogic acid (GA), an active constituent of Garcinia Hanburyi (Teng Huang in Chinese), has been applied for thousands of years for medicinal uses, however, the potential effect of GA in combating cancer resistance remains poorly investigated. In this study, we found that GA could increase the sensitivity of breast cancer cells to TRAIL and enhance TRAIL-induced apoptosis. GA cooperated with TRAIL to decrease the levels of anti-apoptotic proteins and activate Bid (BH3 interacting-domain death agonist) to promote the crosstalk of extrinsic and intrinsic apoptotic signaling, rather than increasing the expression of TRAIL receptors DR4 and DR5. These findings may open a new window in the treatment of breast cancer using TRAIL in combination with GA.
تدمد: 1873-6351
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a722584689f9713ff36dddff0858fef3
https://pubmed.ncbi.nlm.nih.gov/29458160
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....a722584689f9713ff36dddff0858fef3
قاعدة البيانات: OpenAIRE