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Suppression of Intestinal Neoplasia by Deletion of Dnmt3b

机译:通过删除Dnmt3b抑制肠道肿瘤

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摘要

Aberrant gene silencing accompanied by DNA methylation is associated with neoplastic progression in many tumors that also show global loss of DNA methylation. Using conditional inactivation of de novo methyltransferase Dnmt3b in ApcMin/+ mice, we demonstrate that the loss of Dnmt3b has no impact on microadenoma formation, which is considered the earliest stage of intestinal tumor formation. Nevertheless, we observed a significant decrease in the formation of macroscopic colonic adenomas. Interestingly, many large adenomas showed regions with Dnmt3b inactivation, indicating that Dnmt3b is required for initial outgrowth of macroscopic adenomas but is not required for their maintenance. These results support a role for Dnmt3b in the transition stage between microadenoma formation and macroscopic colonic tumor growth and further suggest that Dnmt3b, and by extension de novo methylation, is not required for maintaining tumor growth after this transition stage has occurred.
机译:伴随DNA甲基化的异常基因沉默与许多肿瘤的肿瘤进展有关,这些肿瘤也显示出DNA甲基化的整体丧失。使用Apc Min / + 小鼠中从头甲基转移酶Dnmt3b的条件失活,我们证明了Dnmt3b的丢失对微腺瘤的形成没有影响,这被认为是肠道肿瘤形成的最早阶段。尽管如此,我们观察到宏观结肠腺瘤的形成明显减少。有趣的是,许多大腺瘤显示出具有Dnmt3b失活的区域,这表明Dnmt3b是宏观腺瘤最初生长所必需的,但对其维持却不是必需的。这些结果支持Dnmt3b在微腺瘤形成和宏观结肠肿瘤生长之间的过渡阶段中的作用,并且进一步表明,在此过渡阶段发生后,不需要Dnmt3b以及从头开始进行甲基化来维持肿瘤的生长。

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