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Mechanism of Chinese medicine Fuzheng in reversing paclitaxel resistance in TLR4 over-expressed breast cancer |
ZHANG Xiangjian1, ZHANG Xinxin2, MA Haiguang1, HU Xiaoqing1 |
1.Department of Oncology, Wenzhou Central Hospital, Wenzhou 325000, China; 2.Department of Gynecology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325027, China |
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Cite this article: |
ZHANG Xiangjian,ZHANG Xinxin,MA Haiguang, et al. Mechanism of Chinese medicine Fuzheng in reversing paclitaxel resistance in TLR4 over-expressed breast cancer[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2019, 49(11): 826-831.
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Abstract Objective: To investigate the mechanism of Fuzheng Chinese medicine combined with paclitaxel against TLR4 over-expressing breast cancer, and to confirm the sensitization effect of traditional Chinese medicine combined with chemotherapy for TLR4 over-expressed breast cancer MDA-MB-231 so as to select specific tumor phenotype for combination of traditional Chinese and western medicine. The target provides drug intervention to provide basic data. Methods: MTT assay was used to detect the proliferation inhibition effect of Fuzheng Chinese medicine, paclitaxel and two drugs on breast cancer cell lines T47D and MDA-MB-231. The apoptosis rate was detected by flow cytometry. Expression of the apoptosis related protein and TLR4/NF-kB signaling pathway-associated proteins was detected by Western blotting technology. Results: Fuzheng Chinese medicine and paclitaxel had synergistic effect in the treatment of MDA-MB-231 cell line; Fuzheng Chinese medicine assisted paclitaxel to induce apoptosis of MDA-MB-231 cell line (P<0.05); combined with Chinese medicine and paclitaxel, MDA-MB-231 Cell line TLR4/NF-kB signaling pathway was inhibited (P<0.05). Conclusion: In MDA-MB-231 cell line, Fuzheng Chinese medicine can increase cell apoptosis by inhibiting TLR4/NF-kB signaling pathway, thereby increasing the cell proliferation inhibition effect of paclitaxel on MDA-MB-231 breast cancer cell line and reversing paclitaxel-resistance in breast cancer.
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Received: 24 May 2019
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