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儿童伯基特淋巴瘤中 TP53 通路分析显示,在一部分病例中,只有 MDM4 表达增加是检测到的 TP53 通路异常。

TP53 pathway analysis in paediatric Burkitt lymphoma reveals increased MDM4 expression as the only TP53 pathway abnormality detected in a subset of cases.

机构信息

Department of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT 84112-0565, USA.

出版信息

Br J Haematol. 2012 Sep;158(6):763-71. doi: 10.1111/j.1365-2141.2012.09243.x. Epub 2012 Jul 27.

Abstract

The TP53 (p53) pathway can be inhibited by TP53 mutation or deletion or by MDM2 overexpression. Both occur in Burkitt lymphoma (BL), but many cases lack either abnormality. Expression patterns of the TP53 inhibitor MDM4 have not been reported in BL, and increased MDM4 could deregulate the TP53 pathway in cases without TP53 or MDM2 abnormalities. We investigated TP53 pathway disruption in paediatric BL patient samples (n = 30) by studying MDM4, MDM2, and CDKN1A (p21) protein and mRNA expression; TP53 mutations; TP53 protein expression; and gene copy number abnormalities. MDM4 protein was expressed in 30/30 tumours, and MDM2 protein was weakly expressed in 7/30 (23%). All cases were negative for CDKN1A protein, and CDKN1A mRNA levels were decreased. TP53 mutations were detected in 5/28 (18%) cases and confirmed by sequencing. TP53 protein was expressed in 15/30 (50%) cases, including 7/8 with TP53 genetic alterations. MDM2 protein and mRNA expression levels did not correlate with lack of TP53 genetic changes or TP53 protein expression; however, there was an inverse relationship between detectable TP53 protein expression and MDM4 copy number gains and mRNA expression. The TP53 pathway is deregulated in paediatric BL cases, and increased MDM4 expression may be the primary mechanism in some cases.

摘要

TP53(p53)通路可因 TP53 突变或缺失或 MDM2 过表达而受到抑制。这两种情况均发生于伯基特淋巴瘤(BL)中,但许多病例缺乏这两种异常。TP53 抑制剂 MDM4 的表达模式尚未在 BL 中报道,在没有 TP53 或 MDM2 异常的情况下,MDM4 的增加可能会使 TP53 通路失稳。我们通过研究 MDM4、MDM2 和 CDKN1A(p21)蛋白和 mRNA 表达、TP53 突变、TP53 蛋白表达和基因拷贝数异常,研究了儿科 BL 患者样本(n=30)中 TP53 通路的破坏情况。MDM4 蛋白在 30/30 个肿瘤中表达,MDM2 蛋白在 7/30(23%)个肿瘤中弱表达。所有病例的 CDKN1A 蛋白均为阴性,CDKN1A mRNA 水平降低。在 5/28(18%)例中检测到 TP53 突变,并通过测序证实。TP53 蛋白在 15/30(50%)例中表达,其中 7/8 例存在 TP53 遗传改变。MDM2 蛋白和 mRNA 表达水平与缺乏 TP53 遗传改变或 TP53 蛋白表达无相关性;然而,可检测到的 TP53 蛋白表达与 MDM4 拷贝数增加和 mRNA 表达呈负相关。TP53 通路在儿科 BL 病例中失稳,并且 MDM4 表达增加可能是某些病例中的主要机制。

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