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短期化疗对乳腺癌组织UCH-L1表达的影响

he effect of short-term chemotherapy on the expression of UCH-L1 in breast carcinoma

中文摘要英文摘要

目的 探讨乳腺癌患者术前短期化疗对肿瘤细胞UCH-L1以及EGFR和P-gp表达的影响。方法 采用免疫组化(EnVision法)检测40例乳腺浸润性导管癌患者,MFR药物治疗前后肿瘤细胞UCH-L1、EGFR和P-gp的表达。结果 免疫组化染色显示化疗后肿瘤细胞UCH-L1的表达较化疗前降低(P<0.05),而EGFR的阳性率明显高于化疗前(P<0.01);化疗后P-gp的阳性率也高于化疗前,但无统计学意义。三个标记结果与肿瘤体积缩小和淋巴结转移均无明显相关性。结论 短期MDR药物化疗可以杀伤肿瘤细胞,也可表现出UCH-L1、EGFR和P-gp的变化,其机制可能在于化疗药物对肿瘤细胞选择性损伤所致,也未诱发CD147等下游因子的表达。

Objective  To observe the effects of MDR drugs on the expression of UCH-L1, EGFR and P-gp in the breast carcinoma before and after short-term chemotherapy. Methods The expression of UCH-L1, EGFR and P-gp were assessed by immunohistochemistry (EnVision method) in 40 cases breast carcinoma before and after treatment by MDR drugs (paclitaxel and epirubicin). Results The expression of EGFR was decreased after chemotherapy with MDR drugs(P<0.05). Same as increased EGFR(P<0.01), the expression of P-gp was also increased after chemotherapy, while the changes showed no statistical significance. Negative associations were revealed between UCH-L1, EGFR, and P-gp expression and volume reduce of tumor and LN metastasis. Conclusions Short-term chemotherapy can kill tumor cells and influence the expression of UCH-L1, EGFR, and P-gp. While the involved mechanisms may be the selectivity damage of the MDR drugs on the tumor cells. And also, they are not lead to the expression of CD147 and other downstream factors that enough to cause the invasion of tumor cells.

包芸、唐峰、刘秀萍、陈琦、许祖德、王文娟、李琼

肿瘤学基础医学临床医学

乳腺癌MDR药物泛素羧基末端水解酶1表皮生长因子受体P-糖蛋白免疫组织化学

breast carcinomaMDR drugUCH-L1EGFRP-gpimmunohistochemistry

包芸,唐峰,刘秀萍,陈琦,许祖德,王文娟,李琼.短期化疗对乳腺癌组织UCH-L1表达的影响[EB/OL].(2012-02-17)[2025-08-03].http://www.paper.edu.cn/releasepaper/content/201202-639.点此复制

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