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HOXB13 G84E携带者前列腺肿瘤的体细胞分子亚型分析。

Somatic molecular subtyping of prostate tumors from HOXB13 G84E carriers.

作者信息

Lotan Tamara L, Torres Alba, Zhang Miao, Tosoian Jeffrey J, Guedes Liana B, Fedor Helen, Hicks Jessica, Ewing Charles M, Isaacs Sarah D, Johng Dorhyun, De Marzo Angelo M, Isaacs William B

机构信息

Departments of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Departments of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Oncotarget. 2017 Apr 4;8(14):22772-22782. doi: 10.18632/oncotarget.15196.

Abstract

A recurrent germline mutation (G84E) in the HOXB13 gene is associated with early onset and family history-positive prostate cancer in patients of European descent, occurring in up to 5% of prostate cancer families. To date, the molecular features of prostate tumors occurring in HOXB13 G84E carriers have not been studied in a large cohort of patients. We identified 101 heterozygous carriers of G84E who underwent radical prostatectomy for prostate cancer between 1985 and 2011 and matched these men by race, age and tumor grade to 99 HOXB13 wild-type controls. Immunostaining for HOXB13, PTEN, ERG, p53 and SPINK1 as well as RNA in situ hybridization for ETV1/4/5 were performed using genetically validated assays. Tumors from G84E carriers generally expressed HOXB13 protein at a level comparable to benign and wild-type glands. ETS gene expression (either ERG or ETV1/4/5) was seen in 36% (36/101) of tumors from G84E carriers compared to 68% (65/96) of the controls (p < 0.0001). PTEN was lost in 11% (11/101) of G84E carriers compared to 25% (25/99) of the controls (p = 0.014). PTEN loss was enriched among ERG-positive compared to ERG-negative tumors in both groups of patients. Nuclear accumulation of the p53 protein, indicative of underlying TP53 missense mutations, was uncommon in both groups, occurring in 1% (1/101) of the G84E carriers versus 2% (2/92) of the controls (p = NS). Taken together, these data suggest that genes other than ERG and PTEN may drive carcinogenesis/progression in the majority of men with germline HOXB13 mutations.

摘要

HOXB13基因中的复发性种系突变(G84E)与欧洲血统患者的早发性和家族史阳性前列腺癌相关,在高达5%的前列腺癌家族中出现。迄今为止,尚未在大量患者队列中研究HOXB13 G84E携带者发生的前列腺肿瘤的分子特征。我们确定了101名G84E杂合子携带者,他们在1985年至2011年间因前列腺癌接受了根治性前列腺切除术,并根据种族、年龄和肿瘤分级将这些男性与99名HOXB13野生型对照进行匹配。使用经过基因验证的检测方法对HOXB13、PTEN、ERG、p53和SPINK1进行免疫染色,并对ETV1/4/5进行RNA原位杂交。来自G84E携带者的肿瘤通常表达HOXB13蛋白,其水平与良性和野生型腺体相当。与68%(65/96)的对照相比,36%(36/101)的G84E携带者肿瘤中可见ETS基因表达(ERG或ETV1/4/5)(p<0.0001)。与25%(25/99)的对照相比,11%(11/101)的G84E携带者中PTEN缺失(p = 0.014)。在两组患者中,与ERG阴性肿瘤相比,ERG阳性肿瘤中PTEN缺失更为常见。p53蛋白的核积累表明存在潜在的TP53错义突变,在两组中均不常见,在1%(1/101)的G84E携带者中出现,而在对照中为2%(2/92)(p = 无显著性差异)。综上所述,这些数据表明,除了ERG和PTEN之外,其他基因可能在大多数具有种系HOXB13突变的男性中驱动致癌作用/进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e573/5410261/6551d4c44a70/oncotarget-08-22772-g001.jpg

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