Paris saponin VII reverses chemoresistance in breast MCF-7/ADR cells

التفاصيل البيبلوغرافية
العنوان: Paris saponin VII reverses chemoresistance in breast MCF-7/ADR cells
المؤلفون: Yang Sun, Qibing Mei, Yinbo Niu, Xiao-Qiang Li, Tianle Tang, Hongchuan Jin, Yuhua Li, Ming Xie
المصدر: Journal of Ethnopharmacology. 232:47-54
بيانات النشر: Elsevier BV, 2019.
سنة النشر: 2019
مصطلحات موضوعية: Mice, Nude, Breast Neoplasms, Rhodamine 123, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Nude mouse, In vivo, Drug Discovery, Animals, Humans, Medicine, Cytotoxic T cell, MTT assay, ATP Binding Cassette Transporter, Subfamily B, Member 1, Viability assay, 030304 developmental biology, P-glycoprotein, Pharmacology, Mice, Inbred BALB C, 0303 health sciences, Antibiotics, Antineoplastic, biology, business.industry, Cell growth, Saponins, biology.organism_classification, Antineoplastic Agents, Phytogenic, Tumor Burden, chemistry, Doxorubicin, Drug Resistance, Neoplasm, Trillium, 030220 oncology & carcinogenesis, MCF-7 Cells, biology.protein, Cancer research, Female, business, Phytotherapy
الوصف: Ethnopharmacological relevance The development of a multidrug-resistant (MDR) phenotype is a main obstacle to the successful treatment of breast cancer. Saponins of several herbs are considered as promising candidates for drug resistance treatment. We extracted Paris saponin VII (PS VII) from Trillium tschonoskii Maxim. and investigated whether it could sensitize chemoresistant breast cancer cells MCF-7/ADR to the cytotoxic effects of adriamycin. Materials and methods MCF-7/ADR cells were exposed to 0.5 μM PSVII plus different concentrations of adriamycin (0–100 μM). Then, MTT assay and adriamycin accumulation assay were used to assess cell proliferation and intracellular adriamycin retention. P glycoprotein levels and intracellular rhodamine 123 (Rh-123) accumulations were investigated to measure the expression and activity of P-glycoprotein. A xenograft model of nude mouse was utilized to observe the effect of PSVII in vivo. Results Treatment with PSVII influenced cell viability of MCF-7/ADR cells, as well as sensitized MCF-7/ADR cells to the cytotoxic effects of adriamycin. Moreover, PSVII significantly downregulated MDR1 expression in MCF-7/ADR cells. Intravenous administration of PSVII significantly enhanced anticancer efficacy of adriamycin to MCF-7/ADR xenograft model in nude mice. Conclusion These findings suggested a possible application of PSVII in combination with chemotherapy and/or as neo-adjuvant therapy in the treatment of MDR breast cancer.
تدمد: 0378-8741
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::722c34b0c3b949678e6b32b05520c354Test
https://doi.org/10.1016/j.jep.2018.12.018Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....722c34b0c3b949678e6b32b05520c354
قاعدة البيانات: OpenAIRE