Faneyte Ian F, Kristel Petra M P, van de Vijver Marc J
Department of Experimental Therapy, Cancer Institute / Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Anticancer Res. 2004 Sep-Oct;24(5A):2931-9.
Multidrug resistance associated proteins MRP1, MRP2 and MRP3 confer in vitro multidrug resistance. We investigated their role in breast cancer resistance to anthracycline-based chemotherapy.
Using real-time reverse transcriptase polymerase chain reaction (RT-PCR) and immunohistochemistry (IHC), the expression of MRP1 - 3 was quantified in nine breast cancer cell lines and 30 breast carcinoma samples.
MRP1 - 3 mRNA was detectable in all breast cancer cell lines and tumor samples. No increase of expression was detected between untreated carcinoma and post-neoadjuvant anthracycline treatment tumor samples. IHC failed to detect the proteins. MRP1 - 3 expression was not associated with tumor response to treatment or with outcome.
MRP1 - 3 are expressed in breast cancer cells, but are not detected with IHC. We have found no evidence linking these proteins to clinical drug resistance in a small but well-documented series of breast cancer samples.
多药耐药相关蛋白MRP1、MRP2和MRP3赋予体外多药耐药性。我们研究了它们在乳腺癌对蒽环类化疗耐药中的作用。
使用实时逆转录聚合酶链反应(RT-PCR)和免疫组织化学(IHC),对9种乳腺癌细胞系和30例乳腺癌样本中MRP1 - 3的表达进行定量。
在所有乳腺癌细胞系和肿瘤样本中均检测到MRP1 - 3 mRNA。在未经治疗的癌组织和新辅助蒽环类治疗后的肿瘤样本之间未检测到表达增加。免疫组织化学未能检测到这些蛋白质。MRP1 - 3的表达与肿瘤对治疗的反应或预后无关。
MRP1 - 3在乳腺癌细胞中表达,但免疫组织化学检测不到。在一小系列记录良好的乳腺癌样本中,我们没有发现将这些蛋白质与临床耐药性联系起来的证据。