Objective: To investigate the expression of DBC1 and SIRT1 in advanced breast cancer patients treated by paclitaxel liposome combined with capecitabine, and to provide theoretical basis for the prognosis evaluation. Methods: 80 cases with advanced breast cancer treated in our hospital between July 2013 and July 2015 were chosen as research subjects. Patients were treated with paclitaxel liposome and capecitabine, first day patients were treated with 135-175 mg·m-2 paclitaxel liposome, after that they were treated with capecitabine 2 000 mg·m-2, 21 days as a course of treatment. After treated with 2-6 courses, the expression levels of SIRT1 and DBC1 in the lesions of the patients and in different pathological types were compared, and the adverse reactions were recorded. Results: After treatment the positive rates of SIRT1 and DBC1 expression were significantly lower than before treatment, and the difference was statistically significant(χ2=65.83, P=0.000; χ2=53.43, P=0.000). There was no significant difference in the expression of SIRT1 and DBC1 in different pathological tissues after treatment(P>0.05). The reversible adverse reactions were grade Ⅰ and Ⅱ of hematologic toxicity, hand foot syndrome and digestive tract reaction. By taken the corresponding symptomatic treatment they could be completed in accordance with the original plan chemotherapy, and did not show the liver and kidney function damage and allergic reaction. Conclusion: Patients with advanced breast cancer treated by paclitaxel liposome combined with capecitabine can significantly reduce the positive expression of DBC1 and SIRT1, and has a better security. |
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