Literature DB >> 11214818

SM5-1: a new monoclonal antibody which is highly sensitive and specific for melanocytic lesions.

U Trefzer1, N Rietz, Y Chen, H Audring, G Herberth, P Siegel, S Reinke, P Königer, S Wu, J Ma, Y Liu, H Wang, W Sterry, Y Guo.   

Abstract

Antibodies such as HMB-45 and anti-S100 protein have been widely used as markers of malignant melanoma despite evidence that HMB-45 has a sensitivity of only 67-93% and S100 is nonspecific for melanoma. Using a subtractive immunization protocol in a mouse model of human melanoma, we have generated several monoclonal antibodies with putative specificity for melanoma. After initial screenings, the antibody SM5-1 was chosen because of its intriguing reactivity with melanocytic tumors in both frozen and paraffin sections. The immunohistochemical staining of SM5-1 was studied in paraffin-embedded specimens of 401 melanomas (n = 401; 250 primary melanomas, 151 metastases), melanocytic nevi of the skin (n = 16), nonmelanocytic neoplasms (n = 84). The results were compared with HMB-45 and anti-S100 staining. All antibodies reacted with nevi and 97-99% with primary melanomas. Whereas both SM5-1 and anti-S100 stained 96% (146/151) of melanoma metastases, HMB-45 correctly identified only 83% (126/151). All HMB-45-negative metastases were positive for SM5-1. Whereas neither SM5-1 nor HMB-45 stained any of 84 specimens from 40 different nonmelanocytic neoplasms, anti-S100 was positive in 21/84 (25%). While the staining pattern of SM5-1 was mostly homogeneous, small tumor areas in some metastases remained unstained. Staining with SM5-1 was also observed in perivascular dendritic cells, in plasma cells, some myofibroblasts and the secretion of eccrine sweat glands. Nonactivated epidermal melanocytes, keratinocytes, endothelial cells, smooth muscle cells and peripheral nerves were all negative for SM5-1. These results suggest that SM5-1 is highly specific, as well as sensitive, for melanocytic lesions and is useful in the immunohistochemical evaluation of melanoma.

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Year:  2000        PMID: 11214818     DOI: 10.1007/s004030000186

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.017


  7 in total

1.  Differential expression patterns of capping protein, protein phosphatase 1, and casein kinase 1 may serve as diagnostic markers for malignant melanoma.

Authors:  Daxin Sun; Mian Zhou; Claudia M Kowolik; Vijay Trisal; Qin Huang; Kemp H Kernstine; Fangru Lian; Binghui Shen
Journal:  Melanoma Res       Date:  2011-08       Impact factor: 3.599

2.  Preparation of monoclonal antibody against apoptosis-associated antigens of hepatoma cells by subtractive immunization.

Authors:  Lian-Jun Yang; Wen-Liang Wang
Journal:  World J Gastroenterol       Date:  2002-10       Impact factor: 5.742

3.  Marginal and joint distributions of S100, HMB-45, and Melan-A across a large series of cutaneous melanomas.

Authors:  Hollis Viray; William R Bradley; Kurt A Schalper; David L Rimm; Bonnie E Gould Rothberg
Journal:  Arch Pathol Lab Med       Date:  2013-08       Impact factor: 5.534

Review 4.  Diagnostic and prognostic biomarkers in melanoma.

Authors:  David Weinstein; Jennifer Leininger; Carl Hamby; Bijan Safai
Journal:  J Clin Aesthet Dermatol       Date:  2014-06

5.  The monoclonal antibody SM5-1 recognizes a fibronectin variant which is widely expressed in melanoma.

Authors:  Uwe Trefzer; Yingwen Chen; Gunda Herberth; Maja Ann Hofmann; Felix Kiecker; Yajun Guo; Wolfram Sterry
Journal:  BMC Cancer       Date:  2006-01-11       Impact factor: 4.430

Review 6.  Antibodies to probe endogenous G protein-coupled receptor heteromer expression, regulation, and function.

Authors:  Ivone Gomes; Achla Gupta; Ittai Bushlin; Lakshmi A Devi
Journal:  Front Pharmacol       Date:  2014-12-03       Impact factor: 5.810

Review 7.  lncRNA/MicroRNA interactions in the vasculature.

Authors:  M D Ballantyne; R A McDonald; A H Baker
Journal:  Clin Pharmacol Ther       Date:  2016-03-31       Impact factor: 6.875

  7 in total

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