Department of Anatomy and Cell Biology, Philipps-University, Marburg, Germany.
Cancer Invest. 2012 May;30(4):251-7. doi: 10.3109/07357907.2012.657817. Epub 2012 Apr 5.
The expression of the plasma membrane Ca(2+) ATPase (PMCA) was analyzed in a series of 84 formalin-fixed and paraffin embedded colon samples including normal mucosa (n = 32), adenoma (n = 19), adenocarcinoma (n = 27), and lymph node metastasis (n = 6) using (i) immunohistochemistry, (ii) mRNA in situ hybridization, and (iii) quantitative reverse-transcriptase PCR. A marked reduction of PMCA4 protein was observed in high-grade adenoma, colon cancer as well as lymph node metastasis, pointing to its potential role in the progression of cancer. However, PMCA4 RNA transcripts were unchanged or even increased in colon carcinomas, suggesting posttranscriptional regulation of PMCA4 during carcinogenesis.
采用(i)免疫组织化学,(ii)mRNA 原位杂交和(iii)定量逆转录聚合酶链反应,分析了一系列 84 例福尔马林固定石蜡包埋的结肠样本中的质膜 Ca2+-ATP 酶(PMCA)的表达情况,包括正常黏膜(n = 32)、腺瘤(n = 19)、腺癌(n = 27)和淋巴结转移(n = 6)。在高级别腺瘤、结肠癌和淋巴结转移中,观察到 PMCA4 蛋白表达明显减少,提示其在癌症进展中可能具有潜在作用。然而,结肠癌中 PMCA4 RNA 转录本不变甚至增加,表明在癌变过程中 PMCA4 受到转录后调控。