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HMGA2基因在垂体腺瘤中的关键作用。

Critical role of the HMGA2 gene in pituitary adenomas.

作者信息

Fedele Monica, Pierantoni Giovanna Maria, Visone Rosa, Fusco Alfredo

机构信息

Istituto di Endocrinologia ed Oncologia Sperimentale del CNR, Dipartimento di Biologia e Patologia Cellulare e Molecolare, Università di Napoli Federico II, Naples, Italy.

出版信息

Cell Cycle. 2006 Sep;5(18):2045-8. doi: 10.4161/cc.5.18.3211. Epub 2006 Sep 15.

Abstract

The molecular pathway leading to pituitary tumorigenesis is still largely unknown and is one of the challenges of the endocrine oncology. The development of pituitary adenomas in HMGA2 transgenic mice and the finding of HMGA2 amplification and overexpression in human pituitary adenomas led us to investigate the mechanism by which the HMGA2 gene plays a crucial role in pituitary oncogenesis. This mechanism has been recently described by our group: it entails the acetylation of E2F1, and its consequent enhanced activity, following the displacement of HDAC1 from the pRB/E2F1 inhibitory complex. Based on the mating between HMGA2 transgenic and E2F1 knockout mice, the activation of E2F1 appears to be the main mechanism of the onset of HMGA2-induced pituitary adenoma development. Nevertheless, other events may be also involved in this process, and are discussed here.

摘要

导致垂体肿瘤发生的分子途径在很大程度上仍不清楚,这是内分泌肿瘤学面临的挑战之一。HMGA2转基因小鼠垂体腺瘤的发生以及在人类垂体腺瘤中发现HMGA2扩增和过表达,促使我们研究HMGA2基因在垂体肿瘤发生中发挥关键作用的机制。我们团队最近描述了这一机制:在HDAC1从pRB/E2F1抑制复合物中被取代后,它会导致E2F1乙酰化,进而增强其活性。基于HMGA2转基因小鼠和E2F1基因敲除小鼠的杂交实验,E2F1的激活似乎是HMGA2诱导垂体腺瘤发生的主要机制。然而,其他事件可能也参与了这一过程,本文对此进行了讨论。

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