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Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential

INTRODUCTION: Histologic characteristics cannot adequately predict which patients are at risk of developing metastatic disease after excision of primary cutaneous melanoma. The aim of this study was to identify immunomodulatory genes in primary tumors associated with development of distant metastase...

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Autores principales: Erdrich, Jennifer, Lourdault, Kristel, Judd, Alex, Kaufman, David, Gong, Ke Wei, Gainsbury, Melanie, Deng, Nan, Shon, Wonwoo, Essner, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549765/
https://www.ncbi.nlm.nih.gov/pubmed/35940046
http://dx.doi.org/10.1016/j.jss.2022.06.031
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author Erdrich, Jennifer
Lourdault, Kristel
Judd, Alex
Kaufman, David
Gong, Ke Wei
Gainsbury, Melanie
Deng, Nan
Shon, Wonwoo
Essner, Richard
author_facet Erdrich, Jennifer
Lourdault, Kristel
Judd, Alex
Kaufman, David
Gong, Ke Wei
Gainsbury, Melanie
Deng, Nan
Shon, Wonwoo
Essner, Richard
author_sort Erdrich, Jennifer
collection PubMed
description INTRODUCTION: Histologic characteristics cannot adequately predict which patients are at risk of developing metastatic disease after excision of primary cutaneous melanoma. The aim of this study was to identify immunomodulatory genes in primary tumors associated with development of distant metastases. MATERIALS AND METHODS: Thirty-seven patients with primary melanoma underwent surgical excision. RNA was extracted from the primary tumor specimens. cDNA was synthesized and used with Human Gene Expression microarray. Differential expression of 74 immunomodulatory genes was compared between patients who developed distant metastases and those who did not. RESULTS: Six of 37 patients developed distant metastases during the time of the study. Differential expression of microarray data showed upregulation of four immunomodulatory genes in this group. These four genes—c-CBL, CD276, CXCL1, and CXCL2—were all significantly overexpressed in the metastatic group with differential expression fold change of 1.15 (P = 0.01), 1.16 (P = 0.04), 2.51 (P < 0.001), and 1.68 (P < 0.02), respectively. CXCL1 had particularly high predictive value with an area under the curve of 0.80. Multivariate analysis showed only expression of CXCL1 (P = 0.01) remains predictive of distant metastases in melanoma patients. This result was confirmed using quantitative real-time polymerase chain reaction. CONCLUSIONS: CXCL1, CXCL2, c-CBL, and CD276 are immunomodulatory genes present in primary melanoma that are strongly associated with development of metastatic disease. Identification of their presence, particularly CXCL1, in the primary tumor could be used as a predictor of future risk of metastatic disease and thereby to identify patients who might benefit early from immunotherapy.
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spelling pubmed-95497652022-11-01 Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential Erdrich, Jennifer Lourdault, Kristel Judd, Alex Kaufman, David Gong, Ke Wei Gainsbury, Melanie Deng, Nan Shon, Wonwoo Essner, Richard J Surg Res Article INTRODUCTION: Histologic characteristics cannot adequately predict which patients are at risk of developing metastatic disease after excision of primary cutaneous melanoma. The aim of this study was to identify immunomodulatory genes in primary tumors associated with development of distant metastases. MATERIALS AND METHODS: Thirty-seven patients with primary melanoma underwent surgical excision. RNA was extracted from the primary tumor specimens. cDNA was synthesized and used with Human Gene Expression microarray. Differential expression of 74 immunomodulatory genes was compared between patients who developed distant metastases and those who did not. RESULTS: Six of 37 patients developed distant metastases during the time of the study. Differential expression of microarray data showed upregulation of four immunomodulatory genes in this group. These four genes—c-CBL, CD276, CXCL1, and CXCL2—were all significantly overexpressed in the metastatic group with differential expression fold change of 1.15 (P = 0.01), 1.16 (P = 0.04), 2.51 (P < 0.001), and 1.68 (P < 0.02), respectively. CXCL1 had particularly high predictive value with an area under the curve of 0.80. Multivariate analysis showed only expression of CXCL1 (P = 0.01) remains predictive of distant metastases in melanoma patients. This result was confirmed using quantitative real-time polymerase chain reaction. CONCLUSIONS: CXCL1, CXCL2, c-CBL, and CD276 are immunomodulatory genes present in primary melanoma that are strongly associated with development of metastatic disease. Identification of their presence, particularly CXCL1, in the primary tumor could be used as a predictor of future risk of metastatic disease and thereby to identify patients who might benefit early from immunotherapy. 2022-11 2022-08-05 /pmc/articles/PMC9549765/ /pubmed/35940046 http://dx.doi.org/10.1016/j.jss.2022.06.031 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Erdrich, Jennifer
Lourdault, Kristel
Judd, Alex
Kaufman, David
Gong, Ke Wei
Gainsbury, Melanie
Deng, Nan
Shon, Wonwoo
Essner, Richard
Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential
title Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential
title_full Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential
title_fullStr Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential
title_full_unstemmed Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential
title_short Four Immune Modulating Genes in Primary Melanoma That Predict Metastatic Potential
title_sort four immune modulating genes in primary melanoma that predict metastatic potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549765/
https://www.ncbi.nlm.nih.gov/pubmed/35940046
http://dx.doi.org/10.1016/j.jss.2022.06.031
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