Cargando…

Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.

The c-MET proto-oncogene encodes the receptor for the Hepatocyte Growth Factor/Scatter Factor, which is known to mediate mitogenic, motogenic and invasive responses of several cell types. We have analysed by immunohistochemistry and biochemically the expression of c-MET in benign and malignant melan...

Descripción completa

Detalles Bibliográficos
Autores principales: Natali, P. G., Nicotra, M. R., Di Renzo, M. F., Prat, M., Bigotti, A., Cavaliere, R., Comoglio, P. M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968608/
https://www.ncbi.nlm.nih.gov/pubmed/8104462
_version_ 1782134777811304448
author Natali, P. G.
Nicotra, M. R.
Di Renzo, M. F.
Prat, M.
Bigotti, A.
Cavaliere, R.
Comoglio, P. M.
author_facet Natali, P. G.
Nicotra, M. R.
Di Renzo, M. F.
Prat, M.
Bigotti, A.
Cavaliere, R.
Comoglio, P. M.
author_sort Natali, P. G.
collection PubMed
description The c-MET proto-oncogene encodes the receptor for the Hepatocyte Growth Factor/Scatter Factor, which is known to mediate mitogenic, motogenic and invasive responses of several cell types. We have analysed by immunohistochemistry and biochemically the expression of c-MET in benign and malignant melanocytic lesions. The Met/HGF receptor which in the melanocytic lineage displays the structural features of the authentic receptor was undetectable in tissue melanocytes and in nevocytic nevi. Only four out of 23 primary melanomas scored positive. Expression was increased to a significant level in 17 out of the 44 metastatic lesions examined. The c-MET expression was homogeneous in multiple metastases from the same patients. Comparative analyses showed both lack of correlation with the expression of the tumour progression associated ICAM-1 adhesion molecule and, in 23% of cases, co-expression with the c-KIT encoded receptor. These findings show that the c-MET gene is expressed at late stages of melanoma progression and suggest that the presence of Met/HGF receptor may contribute to the acquisition of an invasive phenotype. IMAGES:
format Text
id pubmed-1968608
institution National Center for Biotechnology Information
language English
publishDate 1993
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-19686082009-09-10 Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression. Natali, P. G. Nicotra, M. R. Di Renzo, M. F. Prat, M. Bigotti, A. Cavaliere, R. Comoglio, P. M. Br J Cancer Research Article The c-MET proto-oncogene encodes the receptor for the Hepatocyte Growth Factor/Scatter Factor, which is known to mediate mitogenic, motogenic and invasive responses of several cell types. We have analysed by immunohistochemistry and biochemically the expression of c-MET in benign and malignant melanocytic lesions. The Met/HGF receptor which in the melanocytic lineage displays the structural features of the authentic receptor was undetectable in tissue melanocytes and in nevocytic nevi. Only four out of 23 primary melanomas scored positive. Expression was increased to a significant level in 17 out of the 44 metastatic lesions examined. The c-MET expression was homogeneous in multiple metastases from the same patients. Comparative analyses showed both lack of correlation with the expression of the tumour progression associated ICAM-1 adhesion molecule and, in 23% of cases, co-expression with the c-KIT encoded receptor. These findings show that the c-MET gene is expressed at late stages of melanoma progression and suggest that the presence of Met/HGF receptor may contribute to the acquisition of an invasive phenotype. IMAGES: Nature Publishing Group 1993-10 /pmc/articles/PMC1968608/ /pubmed/8104462 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Natali, P. G.
Nicotra, M. R.
Di Renzo, M. F.
Prat, M.
Bigotti, A.
Cavaliere, R.
Comoglio, P. M.
Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
title Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
title_full Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
title_fullStr Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
title_full_unstemmed Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
title_short Expression of the c-Met/HGF receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
title_sort expression of the c-met/hgf receptor in human melanocytic neoplasms: demonstration of the relationship to malignant melanoma tumour progression.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968608/
https://www.ncbi.nlm.nih.gov/pubmed/8104462
work_keys_str_mv AT natalipg expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression
AT nicotramr expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression
AT direnzomf expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression
AT pratm expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression
AT bigottia expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression
AT cavalierer expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression
AT comogliopm expressionofthecmethgfreceptorinhumanmelanocyticneoplasmsdemonstrationoftherelationshiptomalignantmelanomatumourprogression