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雌激素受体CpG岛在大多数造血系统肿瘤中发生甲基化。

The estrogen receptor CpG island is methylated in most hematopoietic neoplasms.

作者信息

Issa J P, Zehnbauer B A, Civin C I, Collector M I, Sharkis S J, Davidson N E, Kaufmann S H, Baylin S B

机构信息

Oncology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.

出版信息

Cancer Res. 1996 Mar 1;56(5):973-77.

PMID:8640788
Abstract

Estrogen appears to be a negative regulator of normal hematopoiesis. Chromosome 6q, which contains the estrogen receptor (ER) gene, is frequently altered in human hematopoietic neoplasms. The ER gene, which has growth and metastasis suppressor activity in many different cell types, is inactivated by promoter methylation in some ER-negative breast tumors and 100% of colorectal tumors. We now report that the promoter region of the ER gene is aberrantly methylated in 86% of human hematopoietic tumors, including 8 of 9 pediatric acute lymphocytic leukemia, 17 of 18 adult acute lymphocytic leukemia, 21 of 23 adult acute myelogenous leukemia, 3 of 6 chronic phase chronic myelogenous leukemia, 9 of 9 blast crisis chronic myelogenous leukemia and 5 of 8 lymphomas. This methylation event was also present in all nine leukemia cell lines examined, where it was associated with very low or absent ER expression. In addition, rat and mouse leukemia cell line also exhibited this change, indicating that ER CpG island methylation in leukemias is conserved among species. Our results suggest that ER CpG island methylation could be an important step in the genesis of human hematopoietic neoplasms and might be a useful molecular marker for monitoring the clinical status of these diseases.

摘要

雌激素似乎是正常造血的负调节因子。包含雌激素受体(ER)基因的6号染色体q臂在人类造血肿瘤中经常发生改变。在许多不同细胞类型中具有生长和转移抑制活性的ER基因,在一些ER阴性乳腺癌和100%的结直肠癌中因启动子甲基化而失活。我们现在报告,在86%的人类造血肿瘤中,ER基因的启动子区域存在异常甲基化,包括9例儿童急性淋巴细胞白血病中的8例、18例成人急性淋巴细胞白血病中的17例、23例成人急性髓细胞白血病中的21例、6例慢性期慢性髓细胞白血病中的3例、9例急变期慢性髓细胞白血病中的9例以及8例淋巴瘤中的5例。这种甲基化事件在所有检测的9种白血病细胞系中也存在,且与极低或无ER表达相关。此外,大鼠和小鼠白血病细胞系也表现出这种变化,表明白血病中ER CpG岛甲基化在物种间是保守的。我们的结果表明,ER CpG岛甲基化可能是人类造血肿瘤发生过程中的一个重要步骤,并且可能是监测这些疾病临床状态的一个有用分子标志物。

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