Inhibition of Nrf2 promotes the antitumor effect of Pinelliae rhizome in papillary thyroid cancer
Autor: | Zhi-Peng Du, Sheng Liu, Ming Qiu, Guan-jun Ma, Qiang Wang, Xiang-min Zheng, Jianpeng Jiao, Dao-Zhen Jiang |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
MAPK/ERK pathway Cell Survival MAP Kinase Signaling System NF-E2-Related Factor 2 Physiology Pinellia Clinical Biochemistry Antineoplastic Agents Papillary thyroid cancer 03 medical and health sciences 0302 clinical medicine Downregulation and upregulation Cell Line Tumor medicine Animals Humans Thyroid Neoplasms Viability assay Cell Nucleus Mice Knockout Chemistry Cancer Cell Biology Transfection medicine.disease Mice Inbred C57BL 030104 developmental biology Thyroid Cancer Papillary Apoptosis Cell culture 030220 oncology & carcinogenesis Cancer research Drugs Chinese Herbal |
Zdroj: | Journal of Cellular Physiology. 234:13867-13877 |
ISSN: | 1097-4652 0021-9541 |
Popis: | We previously reported that Xiaotan Sanjie (XTSJ) decoction can prevent the progression of gastric cancer in vitro and in vivo. Pinelliae rhizome (PR), one component of XTSJ decoction, has an inhibitory effect on the growth and proliferation of tumor cells. The present study investigated the underlying mechanisms of action of PR. Using the human papillary thyroid cancer cell lines, TPC-1 and BCPAP, we found that XTSJ decoction and PR alone decreased cell viability to a similar extent in both cell lines, whereas treatment with XTJS decoction without PR [PR (-)] had a lesser effect. PR treatment inhibited the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) in a dose-dependent manner. To investigate the role of Nrf2 in the PR-mediated effects of XTSJ, knockdown of Nrf2 in the tumor cell lines using Nrf2 siRNA (siNrf2) was performed and transfected cells were treated with PR. Silencing of Nrf2 amplified the effects on autophagy, cell viability, apoptosis, and colony formation. Similar results were obtained following treatment with the autophagy inhibitor 3-methyladenine (3-MA). Furthermore, treatment with PR, siNrf2, and/or 3-MA inhibited the MAPK pathway, and analysis of the MAPK pathway components confirmed the role of this pathway in the PR-mediated cellular effects. In mice implanted with siNrf2-transfected cells, the effects of PR were amplified. Taken together, these findings indicate that PR is critical for the inhibitory effects of XTSJ decoction on tumor cell viability and that downregulation of Nrf2 promotes the antitumor effects of PR on papillary thyroid cancer cells. |
Databáze: | OpenAIRE |
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