摘要
目的:评估HER-2过表达乳腺癌患者接受TCH与TAC新辅助化疗后肿瘤恶性程度。方法:86例HER-2过表达乳腺癌患者随机分为观察组及对照组各43例,对照组接受TAC新辅助化疗,观察组接受TCH新辅助化疗,对比两组患者的肿瘤组织侵袭相关指标、自噬相关基因mRNA表达量以及治疗前后血清肿瘤标志物、血管新生分子水平的差异。结果:观察组经TCH新辅助化疗后,乳腺癌组织中侵袭促进分子OPN、CD44v6、CD10的mRNA表达量低于对照组,侵袭抑制分子TIMP-2、TIMP-3的mRNA表达量高于对照组,凋亡相关基因ATG2B、ATG4D、ATG9B、LC3-Ⅱ的mRNA表达量以及LC3-Ⅱ/LC3-I的比例显著高于对照组;治疗后1周时,观察组血清CEA、CA15-3、CA125、VEGF、bFGF水平低于对照组。结论:HER-2过表达乳腺癌患者接受TCH新辅助化疗,可显著降低肿瘤恶性程度,对远期治疗结局的优化有积极意义。
Objective:To evaluate the tumor malignancy in patients with HER-2overexpression breast cancer after TCH and TAC neoadjuvant chemotherapy.Methods:A total of 86 cases of patients with HER-2overexpression breast cancer were randomly divided into observation group and control group(n=43),control group received TAC neoadjuvant chemotherapy,observation group received TCH neoadjuvant chemotherapy,and then the differences in mRNA expression levels of invasion-related indicators and autophagy-related genes in tumor tissue as well as the levels of serum tumor markers and angiogenesis molecules before and after treatment were compared between two groups of patients.Results:After observation group received TCH neoadjuvant chemotherapy,the mRNA expression levels of invasion-promoting molecules OPN,CD44v6 and CD10in breast cancer tissue were lower than those of control group,mRNA expression levels of invasion-inhibiting molecules TIMP-2and TIMP-3 were higher than those of control group,and mRNA expression levels of apoptosis-related genes ATG2 B,ATG4D,ATG9 Band LC3-Ⅱas well as LC3-Ⅱ/LC3-I ratio were significantly higher than those of control group;1week aftertreatment,serum CEA,CA15-3,CA125,VEGF and bFGF levels of observation group were lower than those of control group.Conclusion:TCH neoadjuvant chemotherapy can significantly reduce the tumor malignancy in patients with HER-2overexpression breast cancer,and is of positive significance in optimizing the long-term treatment outcome.
出处
《海南医学院学报》
CAS
2016年第20期2471-2474,共4页
Journal of Hainan Medical University
基金
湖北省教育厅科学研究计划项目(Q20131608)~~
关键词
乳腺癌
HER-2过表达
新辅助化疗
侵袭
自噬
Breast cancer
HER-2overexpression
Neoadjuvant chemotherapy
Invasion
Autophagy