Yang X, Uziely B, Groshen S, Lukas J, Israel V, Russell C, Dunnington G, Formenti S, Muggia F, Press M F
Norris Comprehensive Cancer Center, Department of Pathology, University of Southern California School of Medicine, Los Angeles 90033, USA.
Lab Invest. 1999 Mar;79(3):271-80.
P-glycoprotein (Pgp)-associated multidrug resistance (MDR) is related to intrinsic and acquired cross resistance to anthracyclines, vinca alkaloids, and other antineoplastic antibiotics. Expression of MDR1 is widely considered to play an important role in conferring resistance to adjuvant chemotherapy in women with breast tumor cells in women with disseminated disease, although data supporting this view is, at best, conflicting. The expression of MDR1 gene and its gene product, P-glycoprotein, was investigated in primary and advanced breast cancers (both previously untreated and previously treated on specific treatment protocols) to assess the role of P-glycoprotein in determining responsiveness to adjuvant chemotherapy. Expression was assessed by immunohistochemistry, reverse transcription-PCR (RT-PCR), Northern Blot and Western Blot. MDR1 mRNA was detected in 40% of the breast cancers tested by RT-PCR with 40 cycles of PCR amplification. When reducing the PCR amplification cycles to 28, the MDR1 gene expression signal disappeared from breast cancers of the highest expressers; however, known MDR1 positive control normal tissues, such as adrenal, kidney, and liver continued to show an expression product. Western and Northern blots failed to demonstrate the MDR1 gene product, P-glycoprotein, in these breast cancers. In contrast, physiologic levels of P-glycoprotein was clearly detected in normal adrenal, kidney, and liver by these techniques. Immunohistochemistry confirmed that breast carcinoma cells lacked P-glycoprotein expression; however, interstitial mononuclear cells, morphologically consistent with lymphocytes or macrophages did show immunostaining in some of these breast tumors. MDR1 gene expression identified by RT-PCR was not correlated either with response to paclitaxel therapy (29 patients able to be evaluated, p = 0.34, Fisher Exact Test) or overall survival (32 breast cancer patients with clinical follow-up information, p = 0.336, log rank). In conclusion, P-glycoprotein was not expressed in breast carcinoma cells at significant levels, although it was expressed in stomal lymphocytes or macrophages. These results suggest that P-glycoprotein does not play a significant role in multidrug resistance of breast cancer.
P-糖蛋白(Pgp)相关的多药耐药(MDR)与对蒽环类药物、长春花生物碱及其他抗肿瘤抗生素的内在和获得性交叉耐药有关。多药耐药1(MDR1)的表达在患有播散性疾病的女性乳腺癌细胞中对辅助化疗产生耐药方面被广泛认为起重要作用,尽管支持这一观点的数据充其量也是相互矛盾的。在原发性和晚期乳腺癌(包括既往未治疗和既往按特定治疗方案治疗的)中研究了MDR1基因及其基因产物P-糖蛋白的表达,以评估P-糖蛋白在决定对辅助化疗反应性中的作用。通过免疫组织化学、逆转录聚合酶链反应(RT-PCR)、Northern印迹和Western印迹评估表达情况。通过40个循环的PCR扩增,RT-PCR检测的乳腺癌中有40%检测到MDR1 mRNA。当将PCR扩增循环数减少到28时,最高表达者的乳腺癌中MDR1基因表达信号消失;然而,已知的MDR1阳性对照正常组织,如肾上腺、肾脏和肝脏继续显示出表达产物。Western印迹和Northern印迹未能在这些乳腺癌中证实MDR1基因产物P-糖蛋白。相反,通过这些技术在正常肾上腺、肾脏和肝脏中清楚地检测到了生理水平的P-糖蛋白。免疫组织化学证实乳腺癌细胞缺乏P-糖蛋白表达;然而,形态学上与淋巴细胞或巨噬细胞一致的间质单核细胞在其中一些乳腺肿瘤中确实显示出免疫染色。通过RT-PCR鉴定的MDR1基因表达与对紫杉醇治疗的反应(29例可评估患者,p = 0.34,Fisher确切概率检验)或总生存期(32例有临床随访信息的乳腺癌患者,p = 0.336,对数秩检验)均无相关性。总之,P-糖蛋白在乳腺癌细胞中未大量表达,尽管它在基质淋巴细胞或巨噬细胞中表达。这些结果表明P-糖蛋白在乳腺癌多药耐药中不起重要作用。