FRAME Alternatives Laboratory, Faculty of Medicine and Health Sciences, School of Life Sciences, University of Nottingham, Nottingham, UK.
Gastrointestinal Surgery, Nottingham Digestive Diseases Centre and National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and University of Nottingham, Queen's Medical Centre, Nottingham, NG7 2UH, UK.
Sci Rep. 2023 Oct 3;13(1):16606. doi: 10.1038/s41598-023-43946-6.
Polymeric immunoglobulin receptor (PIGR) has a major role in mucosal immunity as a transporter of polymeric immunoglobulin across the epithelial cells. The aim of this study was to determine the effect of PIGR on cellular behaviours and chemo-sensitivity of MCF7 and MDA-MB468 breast cancer cell lines. Basal levels of PIGR mRNA and protein expression in MCF7 and MDA-MB468 cells were evaluated by real time quantitative polymerase chain reaction and Western blotting, respectively. MCF7/PIGR and MDA-MB468/PIGR stable cell lines, overexpressing the PIGR gene, were generated using a lentiviral vector with tetracycline dependent induction of expression. Cell viability, cell proliferation and chemo-sensitivity of PIGR transfected cells were evaluated and compared with un-transfected cells to determine the effect of PIGR overexpression on cell phenotype. The levels of PIGR mRNA and protein expression were significantly higher in MDA-MB468 cells than in MCF7 cells (380-fold, p < 0.0001). However, the differential expression of PIGR in these two cell lines did not lead to significant differences in chemosensitivity. Viral overexpression of PIGR was also not found to change any of the parameters measured in either cell line. PIGR per se did not affect cellular behaviours and chemosensitivity of these breast cancer cell lines.
多免疫球蛋白受体(PIGR)作为上皮细胞中多免疫球蛋白的转运体,在黏膜免疫中起主要作用。本研究旨在确定 PIGR 对 MCF7 和 MDA-MB468 乳腺癌细胞系细胞行为和化学敏感性的影响。通过实时定量聚合酶链反应和 Western 印迹分别评估 MCF7 和 MDA-MB468 细胞中 PIGR mRNA 和蛋白表达的基础水平。使用带有四环素依赖性表达诱导的慢病毒载体,生成了过表达 PIGR 基因的 MCF7/PIGR 和 MDA-MB468/PIGR 稳定细胞系。评估了 PIGR 转染细胞的细胞活力、细胞增殖和化学敏感性,并将其与未转染细胞进行比较,以确定 PIGR 过表达对细胞表型的影响。与 MCF7 细胞相比,MDA-MB468 细胞中 PIGR mRNA 和蛋白表达水平显著升高(380 倍,p<0.0001)。然而,PIGR 在这两种细胞系中的差异表达并未导致化学敏感性的显著差异。PIGR 的病毒过表达也未改变这两种细胞系中测量的任何参数。PIGR 本身并未影响这些乳腺癌细胞系的细胞行为和化学敏感性。