Literature DB >> 14608901

Diagnostic usefulness of monoclonal antibody P504S in the workup of atypical prostatic glandular proliferations.

Lakshmi P Kunju1, Mark A Rubin, Arul M Chinnaiyan, Rajal B Shah.   

Abstract

We stained 37 prostate needle biopsies and 3 transurethral resections (TURP) containing atypical foci and 20 morphologically unequivocal prostate cancer biopsies, including 4 with foamy features, with P504S. Of 20 biopsies with unequivocal cancer, 18 showed variable P504S staining (sensitivity, 90%); 1 minute cancer and 1 foamy cancer lacked P504S staining. Of 40 cases with atypical foci (biopsies, 37; TURP, 3), 9 were diagnosed as high-grade prostatic intraepithelial neoplasia (HGPIN), 2 were excluded, and 29 had foci of atypical small glandular proliferation. Of these 29 cases, 7 were highly suggestive of cancer, 2 of which lacked P504S staining. In 22 cases with benign atypical foci, 11 were diagnosed as postatrophic hyperplasia (none expressed P504S) and 7 as atypical adenomatous hyperplasia (AAH; 1 showed focal weak P504S staining). Of 9 HGPIN specimens, 8 showed predominantly diffuse, moderate P504S staining. P504S has slightly lower sensitivity for detection of prostate cancer than found previously. Heterogeneous expression patterns may explain negativity in some biopsy specimens with minute cancer. In atypical small glandular proliferations, diffuse positive P504S staining in atypical glands strongly supports a cancer diagnosis, but negative staining does not exclude it. P504S seems to have low sensitivity for detecting foamy prostate cancer. Most HGPINs show diffuse moderate P504S staining. AAH may show focal P504S staining. We recommend using P504S along with morphologic examination and conventional basal cell markers.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14608901     DOI: 10.1309/3T3Y-0K0T-UMYH-3WY2

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  5 in total

Review 1.  [Tissue microarrays. High-throughput procedures to verify potential biomarkers].

Authors:  R Kuefer; M D Hofer; J E Gschwend; M A Rubin
Journal:  Urologe A       Date:  2004-06       Impact factor: 0.639

2.  Diagnostic utility of immunohistochemical markers alpha methyl acyl coA racemase (AMACR) and Ets related gene (ERG) in prostate cancer.

Authors:  Norton Stephen; Bhawana A Badhe
Journal:  Int J Clin Exp Pathol       Date:  2022-09-15

3.  Antibody-based detection of ERG rearrangements in prostate core biopsies, including diagnostically challenging cases: ERG staining in prostate core biopsies.

Authors:  Scott A Tomlins; Nallasivam Palanisamy; Javed Siddiqui; Arul M Chinnaiyan; Lakshmi P Kunju
Journal:  Arch Pathol Lab Med       Date:  2012-08       Impact factor: 5.534

4.  Diagnostic utility of α-methylacyl CoA racemase (P504S) & HMWCK in morphologically difficult prostate cancer.

Authors:  K Kumaresan; Nandita Kakkar; Alka Verma; Arup Kumar Mandal; Shrawan Kumar Singh; Kusum Joshi
Journal:  Diagn Pathol       Date:  2010-12-22       Impact factor: 2.644

5.  Aberrant expression and potency as a cancer immunotherapy target of alpha-methylacyl-coenzyme A racemase in prostate cancer.

Authors:  Ichiya Honma; Toshihiko Torigoe; Yoshihiko Hirohashi; Hiroshi Kitamura; Eiji Sato; Naoya Masumori; Yasuaki Tamura; Taiji Tsukamoto; Noriyuki Sato
Journal:  J Transl Med       Date:  2009-12-09       Impact factor: 5.531

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.