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人类乳腺肿瘤中GATA3的突变

Mutation of GATA3 in human breast tumors.

作者信息

Usary Jerry, Llaca Victor, Karaca Gamze, Presswala Shafaq, Karaca Mehmet, He Xiaping, Langerød Anita, Kåresen Rolf, Oh Daniel S, Dressler Lynn G, Lønning Per E, Strausberg Robert L, Chanock Stephen, Børresen-Dale Anne-Lise, Perou Charles M

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Oncogene. 2004 Oct 7;23(46):7669-78. doi: 10.1038/sj.onc.1207966.

Abstract

GATA3 is an essential transcription factor that was first identified as a regulator of immune cell function. In recent microarray analyses of human breast tumors, both normal breast luminal epithelium and estrogen receptor (ESR1)-positive tumors showed high expression of GATA3. We sequenced genomic DNA from 111 breast tumors and three breast-tumor-derived cell lines and identified somatic mutations of GATA3 in five tumors and the MCF-7 cell line. These mutations cluster in the vicinity of the highly conserved second zinc-finger that is required for DNA binding. In addition to these five, we identified using cDNA sequencing a unique mis-splicing variant that caused a frameshift mutation. One of the somatic mutations we identified was identical to a germline GATA3 mutation reported in two kindreds with HDR syndrome/OMIM #146255, which is an autosomal dominant syndrome caused by the haplo-insufficiency of GATA3. The ectopic expression of GATA3 in human 293T cells caused the induction of 73 genes including six cytokeratins, and inhibited cell line doubling times. These data suggest that GATA3 is involved in growth control and the maintenance of the differentiated state in epithelial cells, and that GATA3 variants may contribute to tumorigenesis in ESR1-positive breast tumors.

摘要

GATA3是一种重要的转录因子,最初被鉴定为免疫细胞功能的调节因子。在最近对人类乳腺肿瘤的微阵列分析中,正常乳腺腔上皮细胞和雌激素受体(ESR1)阳性肿瘤均显示GATA3高表达。我们对111例乳腺肿瘤和3种乳腺肿瘤衍生细胞系的基因组DNA进行了测序,在5例肿瘤和MCF-7细胞系中鉴定出GATA3的体细胞突变。这些突变聚集在DNA结合所需的高度保守的第二个锌指附近。除了这5例,我们通过cDNA测序鉴定出一种独特的错配剪接变体,该变体导致了移码突变。我们鉴定出的一个体细胞突变与在两个患有HDR综合征/OMIM #146255的家族中报道的种系GATA3突变相同,HDR综合征是一种由GATA3单倍体不足引起的常染色体显性综合征。GATA3在人293T细胞中的异位表达导致73个基因的诱导,包括6种细胞角蛋白,并抑制细胞系倍增时间。这些数据表明,GATA3参与上皮细胞的生长控制和分化状态的维持,并且GATA3变体可能有助于ESR1阳性乳腺肿瘤的发生。

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