杨峂|和钢|傅庆国|俞吉霞|黄蓉|李克强. 乳腺癌组织细胞体外对化疗药物敏感性检测结果与GST-πTopoⅡ表达的关系[J]. 中国肿瘤临床, 2011, 38(4): 185-188 . DOI: 10.3969/j.issn.1000-8179.2011.04.002
引用本文: 杨峂|和钢|傅庆国|俞吉霞|黄蓉|李克强. 乳腺癌组织细胞体外对化疗药物敏感性检测结果与GST-πTopoⅡ表达的关系[J]. 中国肿瘤临床, 2011, 38(4): 185-188 . DOI: 10.3969/j.issn.1000-8179.2011.04.002

乳腺癌组织细胞体外对化疗药物敏感性检测结果与GST-πTopoⅡ表达的关系

  • 摘要: 目的:探讨乳腺癌组织细胞体外对化疗药物敏感性检测结果(ATP-TCA法)与GST-π、TopoⅡ表达的关系。方法:用ATP-TCA法检测45例乳腺癌标本对4种常用化疗单药表阿霉素(EPI)、紫杉醇(PTX)、多西紫杉醇 (TXT)、吉西他滨(GEM)及2种联合用药表阿霉素+多西紫杉醇(EPI+TXT)和环磷酰胺+表阿霉素+5-氟尿嘧啶(CEF)的敏感性, 并用免疫组化方法检测乳腺癌组织GST-π、TopoⅡ的表达。结果:ATP-TCA检测结果显示,表阿霉素、紫杉醇、多西紫杉醇、吉西他滨体外对乳腺癌细胞增殖抑制率分别为62.2%、35.6%、8.9%、15.6%;联合用药EPI+TXT、CEF的抑制率分别是77.8%、73.3%,高于单药紫杉醇、多西紫杉醇、吉西他滨,有显著性差异,P<0.01。45例乳腺癌标本中GST-π阳性表达率为44.4%(20/45),TopoⅡ阳性表达率为62.2% (28/45)。在GST-π表达阴性或TopoⅡ表达阳性时,表阿霉素、EPI+TXT及CEF方案对乳腺癌组织细胞增殖抑制率较高, 有显著性差异,P<0.01。结论:ATP-TCA法结合GST-π、 TopoⅡ的表达可用于乳腺癌化疗药物的选择。

     

    Abstract: Correlation of GST-π and Topo ⅡExpression with the Chemosensitivity of Human BreastCancer Cells in vitroTong YANG1, Gang HE1, Qingguo FU1, Jixia YU2, Rong HUANG2, Keqiang LI3Corresponding author: Yang Tong, E-mail:tongyang1@163.com1Department of Oncological Surgery, The Second Hospital of Ningbo City, Ningbo 315010, China2Department of Pathology, The Second Hospital of Ningbo City, Ningbo 315010, China3The Central Laboratory, The Second Hospital of Ningbo City, Ningbo 315010, ChinaAbstract Objective: To investigate the correlation of GST-π and Topo Ⅱ expression with the chemosensitivity of breast cancercells in vitro. Methods: ATP-tumor chemosensitivity assay ( ATP-TCA ) was used to determine the effect of 4 single chemotherapeuticsEpirubicin ( EPI ), Paclitaxel ( PTX ), Taxotere ( TXT ), and Gemcitabine ( GEM ) and 2 combined regimens Epirubicin + Taxotere(EPI + TXT ), Cyclophosphamide + Epirubicin + 5-Fluorouracil ( CEF ) of in vitro breast cancer cells from 45 breast cancer patients.Expression of GST-π and Topo Ⅱ was examined by immunohistrochemistry. Results: ATP-TCA showed that the inhibitory rates ofEPI, PTX, TXT and GFM for breast cancer cell growth were 62.2 %, 35.6 %, 8.9 %, and 15.6 %, respectively. The inhibitory rates ofEPI+TXT and CEF were 77.8 % and 73.3 %, respectively, higher than those of PTX, TXT, and GEM ( P < 0.01 ). Immunohistochemis-try showed that the expression rates of GST-π and TopoⅡ were 44.4 % ( 20/45 ) and 62.2 % ( 28/45 ), respectively. EPI, EPI+TXT andCEF showed higher inhibitory rate in cases with Topo Ⅱ expression or in cases without GST-π expression ( P < 0.01 ). Conclusion:ATP-TCA combined with detection of GST-π and TopoⅡexpression can be used to screen effective therapeutics against breast cancer.Keywords Breast cancer; Chemosensitivity; GST-π; TopoⅡ

     

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