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结直肠癌中CD44v6的下调与CD44启动子区域的高甲基化有关。

Downregulation of CD44v6 in colorectal carcinomas is associated with hypermethylation of the CD44 promoter region.

作者信息

Stallmach A, Wittig B M, Kremp K, Goebel R, Santourlidis S, Zeitz M, Menges M, Raedle J, Zeuzem S, Schulz W A

机构信息

Department of Internal Medicine II, Saarland University, Homburg/Saar, Germany.

出版信息

Exp Mol Pathol. 2003 Jun;74(3):262-6. doi: 10.1016/s0014-4800(03)00025-x.

Abstract

Overexpression of the cell adhesion protein CD44v6 has been demonstrated in colorectal cancer and other gastrointestinal tumors. While CD44v6 is upregulated in benign colorectal adenomas and well-differentiated colorectal cancer tissues, downregulation frequently occurs during disease progression. The mechanism of downregulation, however, is unknown. Therefore, we evaluated the methylation status of the CD44 promoter as a mechanism for decreased CD44v6 expression in advanced colorectal carcinomas. We demonstrated by methylation-sensitive restriction enzyme digestion that the CpG islands of the CD44 promoter were methylated in 6/21 (28%) of benign colorectal adenomas. Interestingly, in colorectal carcinomas the frequency of promoter methylation was significantly increased (10/19; 53%) compared to 7/21 (33%) in the corresponding normal mucosa. Methylation seems to be associated with a more advanced cancer stage, but the trend did not reach statistical significance. In colorectal carcinomas with CD44 promoter methylation CD44v6 mRNA was detected by reverse transcription-polymerase chain reaction in 3/10 carcinomas, whereas in tumors without CD44 promoter methylation CD44v6 expression was observed in 8/9 (P <or= 0.05). These results demonstrated that methylation of the 5'CpG island of the CD44 gene is closely associated with decreased expression of CD44v6 in human colorectal carcinomas.

摘要

细胞黏附蛋白CD44v6在结直肠癌和其他胃肠道肿瘤中呈过表达。虽然CD44v6在良性结直肠腺瘤和高分化结直肠癌组织中上调,但在疾病进展过程中经常出现下调。然而,下调的机制尚不清楚。因此,我们评估了CD44启动子的甲基化状态,作为晚期结直肠癌中CD44v6表达降低的一种机制。我们通过甲基化敏感的限制性内切酶消化证明,在6/21(28%)的良性结直肠腺瘤中,CD44启动子的CpG岛发生了甲基化。有趣的是,与相应正常黏膜中的7/21(33%)相比,结直肠癌中启动子甲基化的频率显著增加(10/19;53%)。甲基化似乎与更晚期的癌症阶段相关,但这一趋势未达到统计学意义。在CD44启动子甲基化的结直肠癌中,通过逆转录-聚合酶链反应在3/10的癌组织中检测到CD44v6 mRNA,而在无CD44启动子甲基化的肿瘤中,8/9观察到CD44v6表达(P≤0.05)。这些结果表明,CD44基因5'CpG岛的甲基化与人结直肠癌中CD44v6表达的降低密切相关。

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