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PLAG1,PLAG基因家族的原型:在肿瘤发生中的多功能性(综述)

PLAG1, the prototype of the PLAG gene family: versatility in tumour development (review).

作者信息

Van Dyck Frederik, Declercq Jeroen, Braem Caroline V, Van de Ven Wim J M

机构信息

Laboratory for Molecular Oncology and Flanders Interuniversity Institute for Biotechnology, Department of Human Genetics, K.U. Leuven, B-3000 Leuven, Belgium.

出版信息

Int J Oncol. 2007 Apr;30(4):765-74.

Abstract

Recent studies of human tumours as well as genetically engineered mouse tumour models have established the importance and versatility of the PLAG1 oncogene in tumourigenesis. The PLAG1 proto-oncogene was discovered by studying the t(3;8)(p21;q12) chromosome translocation, which frequently occurs in human pleomorphic adenomas of the salivary glands. PLAG1 encodes a developmentally regulated, SUMOylated and phosphorylated zinc finger transcription factor, recognizes a specific bipartite DNA consensus sequence regulating expression of a spectrum of target genes, and has two structurally related family members, i.e. the PLAGL1 and PLAGL2 gene. Ectopic PLAG1 overexpression, in many cases due to promoter swapping, causes deregulation of expression of a variety of PLAG1 target genes. This was established by microarray analysis, which indicated that the oncogenic capability of PLAG1 is mediated, at least partly, by the IGF-II mitogenic signaling pathway. Oncogenic activation of PLAG1 is also a crucial event in other human tumours, including lipoblastoma, hepatoblastoma, and AML. The oncogenic potential of PLAG1 has been confirmed in in vitro experiments, which also established IGF-II and IGF-IR as key pathway elements, similarly as in many human tumours. Furthermore, generation of conditional PLAG1 transgenic mouse strains revealed tumour development in a variety of targeted tissues, establishing the versatility of the PLAG1 oncogene and pointing towards a window of opportunity for therapeutic intervention studies. In contrast to the pleiotropic oncogenic potential of PLAG1, its family member PLAGL1, which is localized in an imprinted region on chromosome 6q24-25, is defined by various studies as a tumour-suppressor gene. Finally, the PLAGL2 family member is not only structurally but also functionally more closely related to PLAG1 and has recently also been implicated in AML, both in humans and in genetically modified mice. Collectively, these observations emphasize a more general importance of the PLAG1 gene in tumour development. In light of the fact that IGF-IR is implicated in many human tumours, the diversity in PLAG1-induced mouse tumour models, most of which seem to involve Igf2 signaling, provides useful in vivo platforms to start testing the effects of inhibitors, such as Igf-1r inhibitors, on tumour development in distinct tissues or organ types.

摘要

近期对人类肿瘤以及基因工程小鼠肿瘤模型的研究已经证实了PLAG1癌基因在肿瘤发生过程中的重要性和多功能性。PLAG1原癌基因是通过研究t(3;8)(p21;q12)染色体易位而发现的,这种易位在人类唾液腺多形性腺瘤中经常出现。PLAG1编码一种受发育调控、经SUMO化和磷酸化修饰的锌指转录因子,识别特定的二分DNA共有序列,调控一系列靶基因的表达,并且有两个结构相关的家族成员,即PLAGL1和PLAGL2基因。在许多情况下,由于启动子交换导致的异位PLAG1过表达会引起多种PLAG1靶基因表达的失调。这是通过微阵列分析确定的,该分析表明PLAG1的致癌能力至少部分是由IGF-II促有丝分裂信号通路介导的。PLAG1的致癌激活在其他人类肿瘤中也是一个关键事件,包括脂肪母细胞瘤、肝母细胞瘤和急性髓系白血病(AML)。PLAG1的致癌潜力已在体外实验中得到证实,这些实验同样确定IGF-II和IGF-IR是关键的信号通路元件,与许多人类肿瘤中的情况类似。此外,条件性PLAG1转基因小鼠品系的产生揭示了在多种靶向组织中肿瘤的发生,证实了PLAG1癌基因的多功能性,并为治疗干预研究提供了一个机会窗口。与PLAG1的多效致癌潜力相反,其家族成员PLAGL1定位于6号染色体q24 - 25的印记区域,各种研究将其定义为肿瘤抑制基因。最后,PLAGL2家族成员不仅在结构上而且在功能上与PLAG1更为密切相关,最近在人类和基因修饰小鼠中也被发现与AML有关。总的来说,这些观察结果强调了PLAG1基因在肿瘤发展中更普遍的重要性。鉴于IGF-IR与许多人类肿瘤有关,PLAG1诱导的小鼠肿瘤模型的多样性(其中大多数似乎涉及Igf2信号传导)提供了有用的体内平台,以开始测试抑制剂(如Igf-1r抑制剂)对不同组织或器官类型肿瘤发展的影响。

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