Vidal Igor, Zheng Qizhi, Hicks Jessica L, Chen Jiayu, Platz Elizabeth A, Trock Bruce J, Kulac Ibrahim, Baena-Del Valle Javier A, Sfanos Karen S, Ernst Sarah, Jones Tracy, Maynard Janielle P, Glavaris Stephanie A, Nelson William G, Yegnasubramanian Srinivasan, De Marzo Angelo M
Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States of America.
PLoS One. 2021 Jun 30;16(6):e0241934. doi: 10.1371/journal.pone.0241934. eCollection 2021.
GSTP1 is a member of the Glutathione-S-transferase (GST) family silenced by CpG island DNA hypermethylation in 90-95% of prostate cancers. However, prostate cancers expressing GSTP1 have not been well characterized. We used immunohistochemistry against GSTP1 to examine 1673 primary prostatic adenocarcinomas on tissue microarrays (TMAs) with redundant sampling from the index tumor from prostatectomies. GSTP1 protein was positive in at least one TMA core in 7.7% of cases and in all TMA cores in 4.4% of cases. The percentage of adenocarcinomas from Black patients who had any GSTP1 positive TMA cores was 14.9%, which was 2.5 times higher than the percentage from White patients (5.9%; P < 0.001). Further, the percentages of tumors from Black patients who had all TMA spots positive for GSTP1 (9.5%) was 3-fold higher than the percentage from White patients (3.2%; P<0.001). In terms of association with other molecular alterations, GSTP1 positivity was enriched in ERG positive cancers among Black men. By in situ hybridization, GSTP1 mRNA expression was concordant with protein staining, supporting the lack of silencing of at least some GSTP1 alleles in GSTP1-positive tumor cells. This is the first report revealing that GSTP1-positive prostate cancers are substantially over-represented among prostate cancers from Black compared to White men. This observation should prompt additional studies to determine whether GSTP1 positive cases represent a distinct molecular subtype of prostate cancer and whether GSTP1 expression could provide a biological underpinning for the observed disparate outcomes for Black men.
谷胱甘肽 - S - 转移酶P1(GSTP1)是谷胱甘肽 - S - 转移酶(GST)家族的成员,在90% - 95%的前列腺癌中因CpG岛DNA高甲基化而沉默。然而,表达GSTP1的前列腺癌尚未得到充分表征。我们使用针对GSTP1的免疫组织化学方法,对1673例原发性前列腺腺癌组织微阵列(TMA)进行检测,这些TMA来自前列腺切除术的索引肿瘤,并进行了重复采样。在7.7%的病例中,GSTP1蛋白在至少一个TMA核心中呈阳性,在4.4%的病例中,所有TMA核心均呈阳性。黑人患者中,有任何GSTP1阳性TMA核心的腺癌百分比为14.9%,这比白人患者的百分比(5.9%)高2.5倍(P < 0.001)。此外,黑人患者中所有TMA斑点GSTP1均呈阳性的肿瘤百分比(9.5%)比白人患者的百分比(3.2%)高3倍(P < 0.001)。就与其他分子改变的关联而言,黑人男性中GSTP1阳性在ERG阳性癌症中更为富集。通过原位杂交,GSTP1 mRNA表达与蛋白染色一致,支持GSTP1阳性肿瘤细胞中至少一些GSTP1等位基因没有沉默。这是第一份报告显示,与白人男性相比,GSTP1阳性前列腺癌在黑人前列腺癌中显著过度代表。这一观察结果应促使进一步研究,以确定GSTP1阳性病例是否代表前列腺癌的一种独特分子亚型,以及GSTP1表达是否可以为观察到的黑人男性不同结局提供生物学基础。