A83:与白人男性相比,非裔美国男性局限性前列腺癌患者E3泛素连接酶Nrdp1的核表达降低

Salma Siddiqui, Frank U. Melgoza, B. Durbin-Johnson, R. Vinall, P. Ghosh
{"title":"A83:与白人男性相比,非裔美国男性局限性前列腺癌患者E3泛素连接酶Nrdp1的核表达降低","authors":"Salma Siddiqui, Frank U. Melgoza, B. Durbin-Johnson, R. Vinall, P. Ghosh","doi":"10.1158/1538-7755.DISP17-A83","DOIUrl":null,"url":null,"abstract":"Background: In the U.S., the incidence and mortality rates of prostate cancer (CaP) for African American (AA) men are about 1.5 and 2.3 times higher compared to Caucasian American (CA) men, respectively. CaP is diagnosed at an earlier age and is more aggressive in AA compared to CA patients. The causes for these differences are multifactorial, but include genetic effects that contribute to CaP-associated health disparity. We previously showed that in androgen-dependent CaP cells, the androgen receptor (AR) suppresses levels of the receptor tyrosine kinase ErbB3, a molecule that is known to drive CaP progression, by stimulating the E3 ubiquitin ligase Nrdp1 (also called RNF41 or FLRF). The purpose of the current study was to investigate the role of the AR-Nrdp1-ErbB3 signaling axis in CaP development and progression in AA vs CA men with CaP. Methods: All data were collected with approval from the University of California Davis (UCD) or VA Northern California Health Care System (VANCHCS) Institutional Review Board (IRB). Sections from prostate tumors of 157 patients who underwent radical retropubic prostatectomy at UCD (79) or VANCHCS (78) were analyzed for these studies. Tumor and nontumor areas were identified by a pathologist and 60-µm core samples were extracted from the specific areas of the donor blocks. The specimens were arranged in triplicate in a tissue microarray (TMA) using a Beecher Instruments Manual Tissue Arrayer. Hematoxylin-eosin staining was used as a reference for interpreting the additional sections of the TMA stained with antibodies to Nrdp1 and AR. Results: Nrdp1 has two major proteins isoforms of 317 amino acids (36kDa) and 246 amino acids (28kDa)--both isoforms are expressed in CaP. Subcellular fractionation and immunofluorescence staining of various CaP cell lines showed that while the 36 kDa Nrdp1 was localized to both the cytoplasm and the nucleus, the 28 kDa was localized exclusively in the cytoplasm. Hence, we investigated the expression of Nrdp1 in primary prostate tissues from 157 individual patients, including 19 AA, 121 non-Hispanic CA, 5 Hispanic CA, and 11 others. Using a scoring system based on immunohistochemistry (IHC) scores from 0 to 3, where 0 represents no staining and 3 represents 100% staining, we observed that Nrdp1 was strongly expressed in the epithelial cells of the prostate and could be observed in both the nucleus and the cytoplasm. Comparison of cytoplasmic Nrdp1 levels showed no difference in expression between the different racial groups; however, nuclear Nrdp1 levels differed significantly between races (P = 0.008), with post-hoc testing showing significantly higher expression in CA patients than in AA patients (P = 0.002). Therefore, it is likely that the difference is in the 36-kDa fragment and not the 28-kDa fragment. Further, increased preoperative PSA is associated with significantly higher nuclear Nrdp1 levels (P = 0.030), with a Spearman correlation of 0.19. Finally, we demonstrated that nuclear Nrdp1 levels are significantly higher in subjects without acetylsalicylic acid (aspirin, ASA) use (P = 0.001). Conclusions: Since PSA levels are considered to be a measure of AR transcriptional activity, the correlation between nuclear Nrdp1 and preoperative PSA is supportive of our previous report showing that Nrdp1 is a direct transcriptional target of the AR. Since preoperative PSA is indicative of advanced disease, these results suggest that one reason for higher incidence of CaP and higher CaP progression among AA patients compared to CA is due to the lower levels of nuclear Nrdp1 in the former. Further, since aspirin use increased the levels of nuclear Nrdp1, these data indicate that the use of aspirin may increase nuclear Nrdp1 levels, thereby decreasing the risk of advanced CaP and perhaps reducing CaP disparities between these groups. Citation Format: Salma Siddiqui, Frank U. Melgoza, Blythe P. Durbin-Johnson, Ruth L. Vinall, Paramita M. Ghosh. Decreased nuclear expression of the E3 ubiquitin ligase Nrdp1 in African American men compared to Caucasian men with localized prostate cancer [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr A83.","PeriodicalId":439465,"journal":{"name":"Organ Site Research","volume":"2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abstract A83: Decreased nuclear expression of the E3 ubiquitin ligase Nrdp1 in African American men compared to Caucasian men with localized prostate cancer\",\"authors\":\"Salma Siddiqui, Frank U. Melgoza, B. Durbin-Johnson, R. Vinall, P. Ghosh\",\"doi\":\"10.1158/1538-7755.DISP17-A83\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: In the U.S., the incidence and mortality rates of prostate cancer (CaP) for African American (AA) men are about 1.5 and 2.3 times higher compared to Caucasian American (CA) men, respectively. CaP is diagnosed at an earlier age and is more aggressive in AA compared to CA patients. The causes for these differences are multifactorial, but include genetic effects that contribute to CaP-associated health disparity. We previously showed that in androgen-dependent CaP cells, the androgen receptor (AR) suppresses levels of the receptor tyrosine kinase ErbB3, a molecule that is known to drive CaP progression, by stimulating the E3 ubiquitin ligase Nrdp1 (also called RNF41 or FLRF). The purpose of the current study was to investigate the role of the AR-Nrdp1-ErbB3 signaling axis in CaP development and progression in AA vs CA men with CaP. Methods: All data were collected with approval from the University of California Davis (UCD) or VA Northern California Health Care System (VANCHCS) Institutional Review Board (IRB). Sections from prostate tumors of 157 patients who underwent radical retropubic prostatectomy at UCD (79) or VANCHCS (78) were analyzed for these studies. Tumor and nontumor areas were identified by a pathologist and 60-µm core samples were extracted from the specific areas of the donor blocks. The specimens were arranged in triplicate in a tissue microarray (TMA) using a Beecher Instruments Manual Tissue Arrayer. Hematoxylin-eosin staining was used as a reference for interpreting the additional sections of the TMA stained with antibodies to Nrdp1 and AR. Results: Nrdp1 has two major proteins isoforms of 317 amino acids (36kDa) and 246 amino acids (28kDa)--both isoforms are expressed in CaP. Subcellular fractionation and immunofluorescence staining of various CaP cell lines showed that while the 36 kDa Nrdp1 was localized to both the cytoplasm and the nucleus, the 28 kDa was localized exclusively in the cytoplasm. Hence, we investigated the expression of Nrdp1 in primary prostate tissues from 157 individual patients, including 19 AA, 121 non-Hispanic CA, 5 Hispanic CA, and 11 others. Using a scoring system based on immunohistochemistry (IHC) scores from 0 to 3, where 0 represents no staining and 3 represents 100% staining, we observed that Nrdp1 was strongly expressed in the epithelial cells of the prostate and could be observed in both the nucleus and the cytoplasm. Comparison of cytoplasmic Nrdp1 levels showed no difference in expression between the different racial groups; however, nuclear Nrdp1 levels differed significantly between races (P = 0.008), with post-hoc testing showing significantly higher expression in CA patients than in AA patients (P = 0.002). Therefore, it is likely that the difference is in the 36-kDa fragment and not the 28-kDa fragment. Further, increased preoperative PSA is associated with significantly higher nuclear Nrdp1 levels (P = 0.030), with a Spearman correlation of 0.19. Finally, we demonstrated that nuclear Nrdp1 levels are significantly higher in subjects without acetylsalicylic acid (aspirin, ASA) use (P = 0.001). Conclusions: Since PSA levels are considered to be a measure of AR transcriptional activity, the correlation between nuclear Nrdp1 and preoperative PSA is supportive of our previous report showing that Nrdp1 is a direct transcriptional target of the AR. Since preoperative PSA is indicative of advanced disease, these results suggest that one reason for higher incidence of CaP and higher CaP progression among AA patients compared to CA is due to the lower levels of nuclear Nrdp1 in the former. Further, since aspirin use increased the levels of nuclear Nrdp1, these data indicate that the use of aspirin may increase nuclear Nrdp1 levels, thereby decreasing the risk of advanced CaP and perhaps reducing CaP disparities between these groups. Citation Format: Salma Siddiqui, Frank U. Melgoza, Blythe P. Durbin-Johnson, Ruth L. Vinall, Paramita M. Ghosh. Decreased nuclear expression of the E3 ubiquitin ligase Nrdp1 in African American men compared to Caucasian men with localized prostate cancer [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr A83.\",\"PeriodicalId\":439465,\"journal\":{\"name\":\"Organ Site Research\",\"volume\":\"2 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organ Site Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1158/1538-7755.DISP17-A83\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organ Site Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/1538-7755.DISP17-A83","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景:在美国,非裔美国人(AA)男性前列腺癌(CaP)的发病率和死亡率分别是白人美国人(CA)男性的1.5倍和2.3倍。与CA患者相比,CaP在更早的年龄被诊断出来,并且在AA患者中更具侵略性。造成这些差异的原因是多因素的,但包括遗传影响,导致cap相关的健康差异。我们之前的研究表明,在雄激素依赖性的CaP细胞中,雄激素受体(AR)通过刺激E3泛素连接酶Nrdp1(也称为RNF41或FLRF)来抑制受体酪氨酸激酶ErbB3的水平,ErbB3是一种已知驱动CaP进展的分子。本研究的目的是研究AR-Nrdp1-ErbB3信号轴在AA和CA男性CaP发生和进展中的作用。方法:所有数据均经加州大学戴维斯分校(UCD)或VA北加州医疗保健系统(VANCHCS)机构审查委员会(IRB)批准收集。我们分析了157例在UCD(79)或VANCHCS(78)行根治性耻骨后前列腺切除术的患者的前列腺肿瘤切片。由病理学家鉴定肿瘤和非肿瘤区域,并从供体块的特定区域提取60µm的核心样品。使用比彻仪器手工组织阵列仪将标本一式三份放置于组织微阵列(TMA)中。以苏木精-伊红染色作为参考,解释含有Nrdp1和AR抗体的TMA的附加切片。Nrdp1具有317个氨基酸(36kDa)和246个氨基酸(28kDa)的两种主要蛋白异构体,这两种异构体在CaP中都有表达。对各种CaP细胞系的亚细胞分离和免疫荧光染色显示,36kDa的Nrdp1既定位于细胞质,也定位于细胞核,而28kDa的Nrdp1只定位于细胞质。因此,我们研究了157例个体患者原发性前列腺组织中Nrdp1的表达,包括19例AA, 121例非西班牙裔CA, 5例西班牙裔CA和11例其他患者。采用免疫组化(IHC)评分系统,评分范围从0到3,其中0表示未染色,3表示100%染色,我们观察到Nrdp1在前列腺上皮细胞中强烈表达,并且在细胞核和细胞质中都可以观察到。胞质Nrdp1表达水平在不同种族间无差异;然而,核Nrdp1水平在不同种族之间存在显著差异(P = 0.008),事后检测显示CA患者的表达明显高于AA患者(P = 0.002)。因此,差异很可能是在36 kda片段而不是28 kda片段。此外,术前PSA升高与核Nrdp1水平显著升高相关(P = 0.030), Spearman相关系数为0.19。最后,我们证明了未使用乙酰水杨酸(阿司匹林,ASA)的受试者的核Nrdp1水平明显更高(P = 0.001)。结论:自PSA水平被认为是衡量基于“增大化现实”技术的转录活动,核Nrdp1和术前PSA之间的关系是我们以前的报告显示,支持Nrdp1直接转录目标的基于“增大化现实”技术。由于术前PSA是代表先进的疾病,这些结果表明,帽和发病率高的原因之一帽进展AA患者相比,CA是由于低水平的核Nrdp1前者。此外,由于阿司匹林的使用增加了核Nrdp1的水平,这些数据表明阿司匹林的使用可能增加核Nrdp1的水平,从而降低晚期CaP的风险,并可能减少这些组之间的CaP差异。引文格式:Salma Siddiqui, Frank U. Melgoza, Blythe P. Durbin-Johnson, Ruth L. Vinall, Paramita M. Ghosh。与白人男性相比,非裔美国男性局限性前列腺癌患者E3泛素连接酶Nrdp1的核表达降低[摘要]。见:第十届AACR会议论文集:种族/少数民族和医疗服务不足人群的癌症健康差异科学;2017年9月25-28日;亚特兰大,乔治亚州。费城(PA): AACR;癌症流行病学杂志,2018;27(7增刊):摘要nr A83。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract A83: Decreased nuclear expression of the E3 ubiquitin ligase Nrdp1 in African American men compared to Caucasian men with localized prostate cancer
Background: In the U.S., the incidence and mortality rates of prostate cancer (CaP) for African American (AA) men are about 1.5 and 2.3 times higher compared to Caucasian American (CA) men, respectively. CaP is diagnosed at an earlier age and is more aggressive in AA compared to CA patients. The causes for these differences are multifactorial, but include genetic effects that contribute to CaP-associated health disparity. We previously showed that in androgen-dependent CaP cells, the androgen receptor (AR) suppresses levels of the receptor tyrosine kinase ErbB3, a molecule that is known to drive CaP progression, by stimulating the E3 ubiquitin ligase Nrdp1 (also called RNF41 or FLRF). The purpose of the current study was to investigate the role of the AR-Nrdp1-ErbB3 signaling axis in CaP development and progression in AA vs CA men with CaP. Methods: All data were collected with approval from the University of California Davis (UCD) or VA Northern California Health Care System (VANCHCS) Institutional Review Board (IRB). Sections from prostate tumors of 157 patients who underwent radical retropubic prostatectomy at UCD (79) or VANCHCS (78) were analyzed for these studies. Tumor and nontumor areas were identified by a pathologist and 60-µm core samples were extracted from the specific areas of the donor blocks. The specimens were arranged in triplicate in a tissue microarray (TMA) using a Beecher Instruments Manual Tissue Arrayer. Hematoxylin-eosin staining was used as a reference for interpreting the additional sections of the TMA stained with antibodies to Nrdp1 and AR. Results: Nrdp1 has two major proteins isoforms of 317 amino acids (36kDa) and 246 amino acids (28kDa)--both isoforms are expressed in CaP. Subcellular fractionation and immunofluorescence staining of various CaP cell lines showed that while the 36 kDa Nrdp1 was localized to both the cytoplasm and the nucleus, the 28 kDa was localized exclusively in the cytoplasm. Hence, we investigated the expression of Nrdp1 in primary prostate tissues from 157 individual patients, including 19 AA, 121 non-Hispanic CA, 5 Hispanic CA, and 11 others. Using a scoring system based on immunohistochemistry (IHC) scores from 0 to 3, where 0 represents no staining and 3 represents 100% staining, we observed that Nrdp1 was strongly expressed in the epithelial cells of the prostate and could be observed in both the nucleus and the cytoplasm. Comparison of cytoplasmic Nrdp1 levels showed no difference in expression between the different racial groups; however, nuclear Nrdp1 levels differed significantly between races (P = 0.008), with post-hoc testing showing significantly higher expression in CA patients than in AA patients (P = 0.002). Therefore, it is likely that the difference is in the 36-kDa fragment and not the 28-kDa fragment. Further, increased preoperative PSA is associated with significantly higher nuclear Nrdp1 levels (P = 0.030), with a Spearman correlation of 0.19. Finally, we demonstrated that nuclear Nrdp1 levels are significantly higher in subjects without acetylsalicylic acid (aspirin, ASA) use (P = 0.001). Conclusions: Since PSA levels are considered to be a measure of AR transcriptional activity, the correlation between nuclear Nrdp1 and preoperative PSA is supportive of our previous report showing that Nrdp1 is a direct transcriptional target of the AR. Since preoperative PSA is indicative of advanced disease, these results suggest that one reason for higher incidence of CaP and higher CaP progression among AA patients compared to CA is due to the lower levels of nuclear Nrdp1 in the former. Further, since aspirin use increased the levels of nuclear Nrdp1, these data indicate that the use of aspirin may increase nuclear Nrdp1 levels, thereby decreasing the risk of advanced CaP and perhaps reducing CaP disparities between these groups. Citation Format: Salma Siddiqui, Frank U. Melgoza, Blythe P. Durbin-Johnson, Ruth L. Vinall, Paramita M. Ghosh. Decreased nuclear expression of the E3 ubiquitin ligase Nrdp1 in African American men compared to Caucasian men with localized prostate cancer [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr A83.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信