Nielsen Trine Ostergaard, Friis-Hansen Lennart, Poulsen Steen Seier, Federspiel Birgitte, Sorensen Boe Sandahl
Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus C, Denmark.
Department of Biomedical Sciences, and The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
PLoS One. 2014 Apr 11;9(4):e94606. doi: 10.1371/journal.pone.0094606. eCollection 2014.
Gastric cancer is a major cause of cancer-related deaths in both men and women. The epidermal growth factor receptors are EGFR, HER2, HER3 and HER4. Of the four epidermal growth factor receptors, EGFR and HER2 are well-known oncogenes involved in gastric cancer. Little, however, is known about the role played by HER3 and HER4 in this disease. We obtained paired samples from the tumor and the adjacent normal tissue from the same patient undergoing surgery for gastric cancer. Using RT-qPCR, we quantified the mRNA expression of the four receptors including the HER4 splicing isoforms and all the ligands activating these receptors. Using immunohistochemistry, the protein expression of HER4 was also quantified. We found that HER2 mRNA expression was upregulated in the tumor tissue compared to the matched normal tissue (p = 0.0520). All ligands with affinity for EGFR were upregulated, whereas the expression of EGFR was unchanged. Interestingly, we found the mRNA expression of HER4 (p = 0.0002) and its ligand NRG4 (p = 0.0009) to be downregulated in the tumor tissue compared to the matched normal tissue. HER4 downregulation was demonstrated for all the alternatively spliced isoforms of this receptor. These results support the involvement of EGFR and HER2 in gastric cancer and suggest an interesting association of reduced HER4 expression with development of gastric cancer.
胃癌是男性和女性癌症相关死亡的主要原因。表皮生长因子受体包括EGFR、HER2、HER3和HER4。在这四种表皮生长因子受体中,EGFR和HER2是已知参与胃癌的致癌基因。然而,关于HER3和HER4在这种疾病中所起的作用却知之甚少。我们从接受胃癌手术的同一患者的肿瘤组织和相邻正常组织中获取了配对样本。使用逆转录定量聚合酶链反应(RT-qPCR),我们对包括HER4剪接异构体在内的四种受体以及激活这些受体的所有配体的mRNA表达进行了定量。使用免疫组织化学方法,我们也对HER4的蛋白表达进行了定量。我们发现,与匹配的正常组织相比,肿瘤组织中HER2的mRNA表达上调(p = 0.0520)。所有与EGFR具有亲和力的配体均上调,而EGFR的表达未发生变化。有趣的是,我们发现与匹配的正常组织相比,肿瘤组织中HER4的mRNA表达(p = 0.0002)及其配体NRG4的mRNA表达(p = 0.0009)下调。该受体的所有可变剪接异构体均表现出HER4下调。这些结果支持了EGFR和HER2参与胃癌的发生,并提示HER4表达降低与胃癌发展之间存在有趣的关联。