Cloutier Gabriel, Khalfaoui Taoufik, Carrier Julie C, Beaulieu Jean-François
Laboratory of Intestinal Physiopathology, Department of Immunology and Cell Biology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Department of Medicine, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Int J Mol Sci. 2025 Mar 12;26(6):2564. doi: 10.3390/ijms26062564.
The role of laminin receptors in colorectal cancer (CRC) is the subject of ongoing research. Histopathological studies have suggested that the 67 kDa laminin receptor (67LR) is involved in the carcinogenesis of various malignancies, including CRC. However, the exact composition and nature of 67LR have been a source of confusion for many years. A recent study from our group reported that the 37 kDa form of RPSA participates as a laminin receptor renamed the RPSA-containing laminin receptor (RCLR) but is not the precursor form of the 67LR since the 67 kDa protein associated with 67LR corresponds to the 67 kDa elastin-binding protein (67EBP), which also acts as a laminin receptor. The present study aims to analyze the distinct expression patterns of these two laminin receptor components in CRC. Expressions of RCLR and 67EBP were analyzed in CRC tissues using Western blot and quantitative RT-PCR analyses. The primary colorectal adenocarcinoma tissues and corresponding resection margins showed an overexpression of both RPSA and 67EBP at the protein level in the CRC tissues. An analysis of the publicly available CRC datasets confirmed the overexpression of RPSA and 67EBP in CRC tissues. In conclusion, the elevated expression of these two non-integrin laminin receptors in CRC lesions suggests their critical roles in colorectal carcinogenesis and emphasizes their potential usefulness as tissue biomarkers.
层粘连蛋白受体在结直肠癌(CRC)中的作用是当前研究的主题。组织病理学研究表明,67 kDa层粘连蛋白受体(67LR)参与包括CRC在内的各种恶性肿瘤的致癌过程。然而,多年来67LR的确切组成和性质一直是一个令人困惑的问题。我们小组最近的一项研究报告称,37 kDa形式的RPSA作为层粘连蛋白受体参与其中,重新命名为含RPSA的层粘连蛋白受体(RCLR),但它不是67LR的前体形式,因为与67LR相关的67 kDa蛋白对应于67 kDa弹性蛋白结合蛋白(67EBP),后者也作为层粘连蛋白受体起作用。本研究旨在分析这两种层粘连蛋白受体成分在CRC中的不同表达模式。使用蛋白质印迹法和定量RT-PCR分析在CRC组织中分析RCLR和67EBP的表达。原发性结直肠癌组织和相应的手术切缘显示CRC组织中RPSA和67EBP在蛋白质水平上均过表达。对公开可用的CRC数据集的分析证实了CRC组织中RPSA和67EBP的过表达。总之,这两种非整合素层粘连蛋白受体在CRC病变中的表达升高表明它们在结直肠癌发生中起关键作用,并强调了它们作为组织生物标志物的潜在用途。