期刊文献+

前列腺组织中AMACR表达的临床意义 被引量:2

Expression of α-methylacyl CoA racemase in prostate cancer and its clinical significance
下载PDF
导出
摘要 目的:检测α-甲基酰基辅酶A消旋酶(-αmethylacyl-CoA racemase,AMACR)在前列腺组织中的表达,探索前列腺癌诊断的新方法。方法:前列腺针刺标本108例,用AMACR抗体作免疫组化染色。同时,随机抽取其中的24例病例,每个病例抽取1个针刺标本,用Western blot方法检测AMACR在前列腺癌中的表达,与病理诊断相比较。结果:用免疫组化染色的方法检测AMACR在前列腺癌中的表达,与病理诊断结果相比较,在61例良性标本中,阴性59例,假阳性2例,符合率为96.7%。在44例腺癌中,阳性41例,漏诊3例,符合率为93.2%,总符合率为92.6%。前列腺小细胞癌1例,表达阳性,转移癌1例,表达阴性,高级别前列腺上皮内瘤(high grade prostatic intraepithelial neoplasia,HPIN)1例,表达为弱阳性。用West-ern blot方法检测,与病理诊断结果相比较,符合率为87.5%。在14例良性标本中,阴性14例,假阳性为0,符合率100%。10例癌症标本中,阳性7例,漏诊3例,符合率70%。用免疫组化法检测AMACR在前列腺癌中的表达,可以显示微小癌灶。结论:AMACR是前列腺癌诊断有用的新指标,具有广阔的应用前景。用AMACR结合Western blot,对于前列腺癌的诊断,有一定的临床意义,值得进一步研究。 Objective: To detect the expression of alpha-methylacyl CoA racemase (AMACR) in prostate tissue and to establish a new method for diagnosis of prostate cancer. Methods.. Irnmunohistochemical staining was performed on 108 prostate needle biopsies with AMACR antibodies. Among these cases, western blot analysis was performed on 24 biopsies randomly taken from 24 patients. All the tesls were performed using double-blind method. The results of immunohistochemical staining and western blot were compared with the pathological records. Results:Compared immunohistochemical results with pathological records, 59 out of 65 benign prostatic specimens were AMACR negative and 2 specimens were false-positive. The coincidence rate was 96.7%. In 44 cases of adenocarcinomas, 41 cases were AMACR positive and 3 cases were missed in diagnosis. The coincidence rate of two methods was 93.2% and the total coincidence rate was 92.6%. There was 1 case of prostate small cell carcinoma with AM ACR-positive staining, 1 case of metastatic prostate cancer with AMACR-negative staining, and 1 case of high grade prostatic intraepithelial neoplasia (HPIN) with AMACR-weak positive staining. Compared western blot results with the pathological records, the coincidence rate of lhe two methods was 87.5 %, Fourteen out of 14 benign prostatic specimens were AMACR negative and no specimen was false positive. The coincidence rate was 100%. Seven out of 10 prostate cancer specimens were AMACR-positive and 3 were missed in diagnosis. The coincidence rate was 70%. The results of western blot showed clear bands and definite patterns between positive and neg ative cases. Micro loci of prostate cancers could be found by detecting AMACR expression using immunohistochemical method. Conclusion:AMACR is a new biomarker for prostate cancer diagnosis. Irnmunohistochemical staining for AMACR combined with western blot analysis had clinical significance in the diagnosis of prostate cancer and worthy of further research.
出处 《肿瘤》 CAS CSCD 北大核心 2006年第9期860-862,共3页 Tumor
基金 上海市卫生局科研基金资助项目(编号:024056)
关键词 前列腺肿瘤/诊断 活组织检查 针吸 免疫组织化学 印迹法 蛋白质 α-甲基酰基辅酶A消旋酶 Prostatic neoplasms/diagnosis Biopsy,needle lmmunchistochemistry Blotting,Western α- methylacyl -CoA racemose
  • 相关文献

参考文献10

  • 1PATRIC CW,ALAN BR,ALAN JW, et al. Campbell urology [M]. 8th ed. Philadelphia: Elsevier, 2002:3001-3016.
  • 2THOMPSON IM,PAULER DK,GOODMAN PJ, et al. Prevalence of prostate cancer among men with a prostate-specific antigen level < or = 4.0 ng per milliliter [J]. N Engl J Med, 2004,350(22):2239-2246.
  • 3STEPHENSON RA. Prostate cancer trends in the area of prostate specific -antigen. An update of incidence, mortality, and clinical factors from the SEER database [J]. Urol Clin North Am, 2002,29(1):173-181.
  • 4顾琪.AMACR在前列腺癌中的表达和应用[J].肿瘤,2005,25(2):101-103. 被引量:3
  • 5RUBIN MA,ZHOU M,DHANASEKARAN SM,et al. Alpha-methylacyl CoA racemase as a tissue biomarker for prostate cancer [J]. JAMA, 2002,287(13):1662-1670.
  • 6JAANG Z,WODA BA,WU CL,et al. Discovery and clinical application of a novel prostate cancer marker [J]. Am J Clin Pathol, 2004,122(2):275-289.
  • 7ZHA S,FERDINANDUSSE S,DENIS S,et al. Alpha-methylacyl CoA racemase as an androgen-independent growth modifier in prostate cancer [J]. Cancer Res, 2003,63(21):7365-7376.
  • 8金凡,周淑贞,陶蓉芳,方茹蓉,项永兵,孙璐,高玉堂.上海市区恶性肿瘤发病趋势1972~1994年[J].肿瘤,1999,19(5):255-258. 被引量:73
  • 9上海肿瘤研究所流等病党研究室.1987年上海市区居民恶性肿瘤发病率统计[J].肿瘤,1990,10(3):144-144.
  • 102001年上海市区恶性肿瘤发病率[J].肿瘤,2005,25(6):636-636. 被引量:8

二级参考文献19

  • 1Xu J, Stolk JA, Zhang X, et al. Identification of differentially expressed genes in human prostate cancer using subtraction and microarray[J]. Cancer Res,2000,60:1677-1682.
  • 2Mubiru JN, Shen Ong GL, Valente AJ. et al. Alternative spliced variant of the alpha- methylacyl -CoA racemase gene and their expression in prostate cancer [J]. Gene, 2004,327:89-98.
  • 3Thompson IM, Pauler DK, Goodman PJ, et al. Prevalence of prostate cancer among men with a prostate-specific antigen level < or =4. 0 ng per milliliter[J]. N Engl J Med,2004,350: 2239-2246.
  • 4Stephenson RA. Prostate cancer trends in the area of prostate-specific antigen. An update of incidence, mortality, and clinical factors from the SEER database [ J ]. Urol. Clin.North. Am, 2002,29:173-181.
  • 5Luo J, Zha S, Gage WR, et al. Alpha-methylacyl CoA racemase: a new molecular marker for prostate cancer[J]. Cancer Rees, 2002,62: 2220-2226.
  • 6Zheng SL,Chang BL, Faith DA,et al. Sequence varuants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk[J]. Cancer Res,2002,62:6485-6488.
  • 7Jiang Z, Woda BA, Rock KL, et al. P504S: a new molecular marker for the detection of prostate cancer[J]. Am J Surg Pathol,2001,25:1397-1404.
  • 8Rubin MA, Zhou M, Dhanasekaran SM, et al. Alpha-methylacyl CoA racemase as a tissue biomarker for prostate cancer[J]. JAMA, 2002,287:1662-1670.
  • 9Shan Zha, Saohe Ferdinandusse, Simone Denis et al. Alphamethylacyl CoA racemase as an androgen-independent growth modifier in prostate cancer[J]. Ca ncer Res,2003,63:7365-7376.
  • 10Beach R, Gown AM, Peralta Venturina MN, et al. P504S immunohistochemical detection in 405 prostatic specimens including 376 18-gauge needle biopsies[J]. Am J Surg Pathol,2002,26:1588-1596.

共引文献81

同被引文献26

  • 1顾琪.AMACR在前列腺癌中的表达和应用[J].肿瘤,2005,25(2):101-103. 被引量:3
  • 2盛璐,宋建达,顾琪,肖立,孙忠全,钱伟庆.α-甲酰辅酶A消旋酶免疫组化染色——诊断前列腺癌的新方法[J].中华泌尿外科杂志,2005,26(6):375-378. 被引量:5
  • 3卫生部中国癌症预防与控制规划纲要(2004-2010).http://www.moh.gov.cn/uploadfile/200409/2004028104540901.doc.
  • 4Iczkowski KA, 2iang Z, Tretiakova M, et al. Prostatic needle biopsies with suspicious (ASAP) diagnosis: 80% resolved using P504S/AMACR and keration34E12 immunostaining [J]. Mod Pathol, 2003,16: 154A.
  • 5Jian-feng Lin, Jun Xu, Hong-yu, et al. Identification of candidate prostate cancer biomarkers in prostate needle biopsy specimens using proteomic analysis [J]. Int J Cancer, 2007,121: 2596-2605.
  • 6Li D, Butch P, Gonzalez O, et al. Molecular cloning, expression analysis, and chromosome mapping of WDR6, a novel human WD-repeat gene [J]. 2000,274 (1): 117-123.
  • 7Efimenko E, Blacque OE, Ou G, et al. Caenorhabditis elegans DYF-2, an Orthologue of Human WDR19, Is a Com- ponent of the Intraflagellar Transport Machinery in Sensory Cilia [J]. Mol Biol Cell, 2006,17 (11): 4801-4811.
  • 8Lin B, White JT, Utleg AG, et al. Isolation and characterization of human and mouse WDR19, a novel WD- repeat protein exhibiting androgen-regulated expression in prostare epithelium [J]. Genomics, 2003, 82 (3): 331-342.
  • 9Lin B, Utleg AG, Gravdal K, et al. WDR19 expression is increased in prostate cancer compared with normal cells, but low-intensity expression in cancers is associated with shorter time to biochemical failures and local recurrence [J]. Clin Cancer Res, 2008,14 (5): 1397-1406.
  • 10Xu J,Stolk JA,Zhang X,et al.Identification of differentially expressed genes in human prostate cancer using subtraction and microarray.Cancer Res,2000,60:1677~1682.

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部