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T 细胞急性淋巴细胞白血病中蛋白酪氨酸磷酸酶基因 PTPN2 的缺失。

Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia.

机构信息

Department of Molecular and Developmental Genetics, VIB, Leuven, Belgium.

出版信息

Nat Genet. 2010 Jun;42(6):530-5. doi: 10.1038/ng.587. Epub 2010 May 16.

Abstract

PTPN2 (protein tyrosine phosphatase non-receptor type 2, also known as TC-PTP) is a cytosolic tyrosine phosphatase that functions as a negative regulator of a variety of tyrosine kinases and other signaling proteins. In agreement with its role in the regulation of the immune system, PTPN2 was identified as a susceptibility locus for autoimmune diseases. In this work, we describe the identification of focal deletions of PTPN2 in human T-cell acute lymphoblastic leukemia (T-ALL). Deletion of PTPN2 was specifically found in T-ALLs with aberrant expression of the TLX1 transcription factor oncogene, including four cases also expressing the NUP214-ABL1 tyrosine kinase. Knockdown of PTPN2 increased the proliferation and cytokine sensitivity of T-ALL cells. In addition, PTPN2 was identified as a negative regulator of NUP214-ABL1 kinase activity. Our study provides genetic and functional evidence for a tumor suppressor role of PTPN2 and suggests that expression of PTPN2 may modulate response to treatment.

摘要

PTPN2(蛋白酪氨酸磷酸酶非受体 2 型,也称为 TC-PTP)是一种胞质酪氨酸磷酸酶,作为多种酪氨酸激酶和其他信号蛋白的负调节剂发挥作用。与它在免疫系统调节中的作用一致,PTPN2 被确定为自身免疫性疾病的易感性位点。在这项工作中,我们描述了人 T 细胞急性淋巴细胞白血病(T-ALL)中 PTPN2 的局灶性缺失的鉴定。PTPN2 的缺失特异性地存在于 TLX1 转录因子致癌基因异常表达的 T-ALL 中,包括四个也表达 NUP214-ABL1 酪氨酸激酶的病例。PTPN2 的敲低增加了 T-ALL 细胞的增殖和细胞因子敏感性。此外,PTPN2 被鉴定为 NUP214-ABL1 激酶活性的负调节剂。我们的研究为 PTPN2 的肿瘤抑制作用提供了遗传和功能证据,并表明 PTPN2 的表达可能调节对治疗的反应。

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