Cross H S, Bajna E, Bises G, Genser D, Kállay E, Pötzi R, Wenzl E, Wrba F, Roka R, Peterlik M
Department of General and Experimental Pathology, University Hospital (AKH), Vienna, Austria.
Anticancer Res. 1996 Jul-Aug;16(4B):2333-7.
Epidemiological data suggest the protective role of vitamin D against the development of colorectal carcinoma in man. This could be due to the anti-mitogenic effect of the steroid hormone on human colon carcinoma cells which is mediated by a specific nuclear vitamin D receptor (VDR). Western blot analysis showed that VDR expression increases during the transition from normal mucosa to polyps and later to pT3 tumors. In later stages, however, VDR is dramatically reduced. Cytokeratin 20, which was monitored as a differentiation marker, decreases in parallel with advancing proliferation and disappears from "normal" mucosa adjacent to later stage carcinoma. Interestingly, VDR density was conspicuously higher in all tumors tested when compared to adjacent "normal" tissue. This suggest that, up to a certain degree of dedifferentiation, malignant colonocytes can upregulate the VDR, probably as a counteractive measure in response to tumor cell growth, but that this ability is finally lost in highly undifferentiated carcinoma cells.
流行病学数据表明维生素D对人类结直肠癌的发生具有保护作用。这可能是由于这种类固醇激素对人结肠癌细胞具有抗有丝分裂作用,该作用由特异性核维生素D受体(VDR)介导。蛋白质免疫印迹分析表明,在从正常黏膜向息肉以及随后向pT3肿瘤转变的过程中,VDR表达增加。然而,在后期阶段,VDR显著减少。作为分化标志物进行监测的细胞角蛋白20,随着增殖的进展而平行减少,并从晚期癌旁的“正常”黏膜中消失。有趣的是,与相邻的“正常”组织相比,在所有测试的肿瘤中VDR密度明显更高。这表明,在一定程度的去分化之前,恶性结肠细胞可以上调VDR,这可能是作为对肿瘤细胞生长的一种对抗措施,但这种能力最终在高度未分化的癌细胞中丧失。