Anti-oral cancer effects of triptolide by downregulation of DcR3 in vitro, in vivo, and in preclinical patient-derived tumor xenograft model

التفاصيل البيبلوغرافية
العنوان: Anti-oral cancer effects of triptolide by downregulation of DcR3 in vitro, in vivo, and in preclinical patient-derived tumor xenograft model
المؤلفون: Chun-Chieh Ting, Gu-Jiun Lin, Yen‐Tzu Chen, Huey-Kang Sytwu, Chun-Shu Lin, Chang-Huei Tsao, Wei-Chin Chang, Yuan-Wu Chen, Cheng-Chih Hsieh, Chih-Kung Lin, Bo Peng, Cheng-Yu Yang
المصدر: Head & Neck
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Down-Regulation, metastasis‐associated protein 1 (MTA1), 03 medical and health sciences, chemistry.chemical_compound, Mice, 0302 clinical medicine, Downregulation and upregulation, In vivo, Mice, Inbred NOD, patient‐derived tumor xenograft (PDTX), Biomarkers, Tumor, Medicine, Animals, Humans, Antineoplastic Agents, Alkylating, Cell Proliferation, business.industry, Cell growth, Receptors, Tumor Necrosis Factor, Member 6b, Cancer, Original Articles, Triptolide, Phenanthrenes, medicine.disease, Immunohistochemistry, Xenograft Model Antitumor Assays, decoy receptor 3 (DcR3), 030104 developmental biology, Otorhinolaryngology, chemistry, Cell culture, oral squamous cell carcinoma (OSCC), 030220 oncology & carcinogenesis, triptolide, Cancer research, Carcinoma, Squamous Cell, Epoxy Compounds, Heterografts, Mouth Neoplasms, Original Article, Decoy receptor 3, Diterpenes, business
الوصف: Background Aberrant expression of decoy receptor 3 (DcR3) is considered to be a diagnostic and therapeutic target for human cancers. The aim of this study was to assess DcR3 as a target of the anticancer effects of triptolide (TPL) in preclinical patient‐derived tumor xenograft (PDTX) models of oral squamous cell carcinoma (OSCC). Methods The expression of DcR3 was evaluated through immunohistochemistry, and correlations were examined using clinical variables. The effects of TPL on the expression of DcR3 and cell proliferation were investigated in OSCC cell lines and in PDTX models. Results DcR3 overexpression was associated with overall survival and tumor size. TPL significantly decreased tumor growth. Moreover, TPL inhibited the expression of metastasis‐associated protein 1 (MTA1), a transcription factor for DcR3 in vivo, in vitro, and in PDTX models. Conclusion TPL appeared to exert anticancer effects by repressing DcR3 and MTA1 in vitro, in vivo, and in PDTX models.
تدمد: 1097-0347
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de04c4b4b04fe17f879bc7e952ef0e71Test
https://pubmed.ncbi.nlm.nih.gov/30537218Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....de04c4b4b04fe17f879bc7e952ef0e71
قاعدة البيانات: OpenAIRE