Literature DB >> 8504426

Association of high molecular weight melanoma-associated antigen expression in primary acral lentiginous melanoma lesions with poor prognosis.

T Kageshita1, N Kuriya, T Ono, T Horikoshi, M Takahashi, G Y Wong, S Ferrone.   

Abstract

In a recent study we detected marked differences in the antigenic profile of acral lentiginous melanoma (ALM) and nodular melanoma lesions. Furthermore, we showed that the human high molecular weight melanoma-associated antigen (HMW-MAA) is expressed with a significantly higher frequency in metastatic than in primary ALM lesions. Because of the potential role of HMW-MAA in the metastatic process of melanoma cells, in the present investigation we tested whether HMW-MAA represents a useful prognostic marker in ALM. Primary ALM lesions removed from 32 patients were stained with anti-HMW-MAA monoclonal antibody (mAb) in an immunoperoxidase reaction. The results were correlated with the expression of other markers defined by mAb, with clinical parameters of the disease, and with histopathological characteristics of the lesions. Only 9 of the 32 primary ALM lesions tested were stained by anti-HMW-MAA mAb. Expression of HMW-MAA was the only variable associated with patients' survival and disease-free survival. Both were significantly shorter in patients with HMW-MAA expression in their primary lesions. These results suggest that HMW-MAA may represent a novel prognostic marker in ALM, since phenotyping of primary ALM lesions with anti-HMW-MAA mAb may provide information about the prognosis of the disease which cannot be obtained with known prognostic parameters.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8504426

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  8 in total

1.  Chondroitin sulfate proteoglycan 4 enhanced melanoma motility and growth requires a cysteine in the core protein transmembrane domain.

Authors:  Jianbo Yang; Matthew A Price; Leah E C Wanshura; Jinsong He; Mei Yi; Danny R Welch; Guiyuan Li; Sean Conner; Jonathan Sachs; Eva A Turley; James B McCarthy
Journal:  Melanoma Res       Date:  2019-08       Impact factor: 3.599

Review 2.  Antithetic roles of proteoglycans in cancer.

Authors:  Elena Garusi; Silvia Rossi; Roberto Perris
Journal:  Cell Mol Life Sci       Date:  2011-10-02       Impact factor: 9.261

3.  Retrovirus targeting by tropism restriction to melanoma cells.

Authors:  F Martin; S Neil; J Kupsch; M Maurice; F Cosset; M Collins
Journal:  J Virol       Date:  1999-08       Impact factor: 5.103

4.  CSPG4 protein as a new target for the antibody-based immunotherapy of triple-negative breast cancer.

Authors:  Xinhui Wang; Takuya Osada; Yangyang Wang; Ling Yu; Koichi Sakakura; Akihiro Katayama; James B McCarthy; Adam Brufsky; Mamatha Chivukula; Thaer Khoury; David S Hsu; William T Barry; H Kim Lyerly; Timothy M Clay; Soldano Ferrone
Journal:  J Natl Cancer Inst       Date:  2010-09-17       Impact factor: 13.506

Review 5.  Diagnostic and prognostic biomarkers in melanoma.

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

6.  CSPG4 as a prognostic biomarker in chordoma.

Authors:  Andrew J Schoenfeld; Xinhui Wang; Yangyang Wang; Francis J Hornicek; G Petur Nielsen; Zhenfeng Duan; Soldano Ferrone; Joseph H Schwab
Journal:  Spine J       Date:  2015-12-09       Impact factor: 4.166

7.  Melanoma chondroitin sulfate proteoglycan enhances FAK and ERK activation by distinct mechanisms.

Authors:  Jianbo Yang; Matthew A Price; Cheryl L Neudauer; Christopher Wilson; Soldano Ferrone; Hong Xia; Joji Iida; Melanie A Simpson; James B McCarthy
Journal:  J Cell Biol       Date:  2004-06-21       Impact factor: 10.539

Review 8.  Theranostic impact of NG2/CSPG4 proteoglycan in cancer.

Authors:  Pier Andrea Nicolosi; Alice Dallatomasina; Roberto Perris
Journal:  Theranostics       Date:  2015-02-15       Impact factor: 11.556

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.