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肺耐药相关蛋白(LRP)在正常及肿瘤性人呼吸道细胞中的免疫定位与细胞表达

Immunolocalization and cell expression of lung resistance-related protein (LRP) in normal and tumoral human respiratory cells.

作者信息

Bouhamyia Lamiaâ, Chantot-Bastaraud Sandra, Zaidi Sakina, Roynard Patricia, Prengel Claudie, Bernaudin Jean-François, Fleury-Feith Jocelyne

机构信息

Service d'Histologie et Biologie Tumorale, Hôpital Tenon, 4 rue de la chine, 75020, Paris, France.

出版信息

J Histochem Cytochem. 2007 Aug;55(8):773-82. doi: 10.1369/jhc.7A7176.2007. Epub 2007 Apr 16.

Abstract

Lung resistance-related protein (LRP) is an integral part of the multidrug resistance (MDR) phenotype involved in cell resistance toward xenobiotics or chemotherapy. The aim of this study was to compare the intracellular localization and cell expression of LRP in normal bronchial cells and their tumoral counterparts from non-small cell lung cancer (NSCLC). LRP expression was also investigated concurrently with DNA ploidy and chromosome 16 (lrp gene locus) aberrations. Confocal microscopy showed that LRP localization was exclusively intracytoplasmic regardless of the cell type and was never observed in the nuclear pore complex. Flow cytometry demonstrated a similar level of LRP expression in normal bronchial cells and in cancer cells from NSCLC samples. FISH analysis, performed to evaluate the number of chromosome 16 and lrp loci, demonstrated a significant gain of chromosome 16 in DNA aneuploid tumors. Furthermore, we did not find any link between LRP expression and DNA ploidy status or chromosome 16 number. These results suggest that LRP expression observed in NSCLC, maintained through the carcinogenesis process of respiratory cells, is not altered by the increased number of copies of chromosome 16 and probably controlled by mechanisms different from those of MRP1 expression, whereas both proteins are associated with the MDR phenotype.

摘要

肺耐药相关蛋白(LRP)是多药耐药(MDR)表型的一个组成部分,参与细胞对外源化合物或化疗的耐药。本研究的目的是比较正常支气管细胞及其非小细胞肺癌(NSCLC)肿瘤对应细胞中LRP的细胞内定位和细胞表达。同时还研究了LRP表达与DNA倍体及16号染色体(lrp基因位点)畸变的关系。共聚焦显微镜显示,无论细胞类型如何,LRP定位均仅在细胞质内,从未在核孔复合体中观察到。流式细胞术表明,正常支气管细胞和NSCLC样本中的癌细胞中LRP表达水平相似。为评估16号染色体和lrp基因位点数量而进行的荧光原位杂交(FISH)分析表明,DNA非整倍体肿瘤中16号染色体有显著增加。此外,我们未发现LRP表达与DNA倍体状态或16号染色体数量之间存在任何关联。这些结果表明,在NSCLC中观察到的LRP表达在呼吸细胞的致癌过程中得以维持,不受16号染色体拷贝数增加的影响,可能由不同于多药耐药相关蛋白1(MRP1)表达的机制控制,而这两种蛋白均与MDR表型相关。

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