Cargando…

Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis

Skin cutaneous melanoma (SKCM) is the most aggressive type of skin cancer, with a high rate of metastasis and mortality; however, identification of biomarkers for the treatment of SKCM is required. Cluster of differentiation (CD)38 has emerged as an effective target for therapeutic drugs in several...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xianwang, Wang, Pengli, Ge, Lei, Wang, Juan, Naqvi, Syed Manzar Abbas Shah, Hu, Shujuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7405635/
https://www.ncbi.nlm.nih.gov/pubmed/32774485
http://dx.doi.org/10.3892/ol.2020.11873
_version_ 1783567286286680064
author Wang, Xianwang
Wang, Pengli
Ge, Lei
Wang, Juan
Naqvi, Syed Manzar Abbas Shah
Hu, Shujuan
author_facet Wang, Xianwang
Wang, Pengli
Ge, Lei
Wang, Juan
Naqvi, Syed Manzar Abbas Shah
Hu, Shujuan
author_sort Wang, Xianwang
collection PubMed
description Skin cutaneous melanoma (SKCM) is the most aggressive type of skin cancer, with a high rate of metastasis and mortality; however, identification of biomarkers for the treatment of SKCM is required. Cluster of differentiation (CD)38 has emerged as an effective target for therapeutic drugs in several types of cancer, such as chronic lymphocytic leukemia and multiple myeloma. In the present study, to determine the contribution of CD38 to the diagnosis of SKCM, Gene Expression Profiling Interactive Analysis 2 and University of Alabama Cancer Database online tools were used to analyze The Cancer Genome Atlas-SKCM dataset. Moreover, Search Tool for the Retrieval of Interacting Genes/Proteins and GeneMANIA databases were used to determine protein-protein interaction networks and potential functions. To the best of our knowledge, the results of the present study indicated for the first time that high expression levels of CD38 were a favorable diagnostic factor for SKCM. Moreover, a correlation between CD38 expression levels and the survival probability of patients with SKCM was identified. Integrative analysis predicted that nine genes were correlated with CD38 in SKCM, and the similarity of these genes in SKCM expression and a survival heatmap was verified. Gene ontology enrichment analysis using the Metascape tool revealed that CD38 and its correlated genes were significantly enriched in lymphocyte activation and T cell differentiation regulation. Collectively, the bioinformatics analysis revealed that CD38 might serve as a potential diagnostic predictor for SKCM.
format Online
Article
Text
id pubmed-7405635
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-74056352020-08-06 Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis Wang, Xianwang Wang, Pengli Ge, Lei Wang, Juan Naqvi, Syed Manzar Abbas Shah Hu, Shujuan Oncol Lett Articles Skin cutaneous melanoma (SKCM) is the most aggressive type of skin cancer, with a high rate of metastasis and mortality; however, identification of biomarkers for the treatment of SKCM is required. Cluster of differentiation (CD)38 has emerged as an effective target for therapeutic drugs in several types of cancer, such as chronic lymphocytic leukemia and multiple myeloma. In the present study, to determine the contribution of CD38 to the diagnosis of SKCM, Gene Expression Profiling Interactive Analysis 2 and University of Alabama Cancer Database online tools were used to analyze The Cancer Genome Atlas-SKCM dataset. Moreover, Search Tool for the Retrieval of Interacting Genes/Proteins and GeneMANIA databases were used to determine protein-protein interaction networks and potential functions. To the best of our knowledge, the results of the present study indicated for the first time that high expression levels of CD38 were a favorable diagnostic factor for SKCM. Moreover, a correlation between CD38 expression levels and the survival probability of patients with SKCM was identified. Integrative analysis predicted that nine genes were correlated with CD38 in SKCM, and the similarity of these genes in SKCM expression and a survival heatmap was verified. Gene ontology enrichment analysis using the Metascape tool revealed that CD38 and its correlated genes were significantly enriched in lymphocyte activation and T cell differentiation regulation. Collectively, the bioinformatics analysis revealed that CD38 might serve as a potential diagnostic predictor for SKCM. D.A. Spandidos 2020-10 2020-07-15 /pmc/articles/PMC7405635/ /pubmed/32774485 http://dx.doi.org/10.3892/ol.2020.11873 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, Xianwang
Wang, Pengli
Ge, Lei
Wang, Juan
Naqvi, Syed Manzar Abbas Shah
Hu, Shujuan
Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
title Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
title_full Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
title_fullStr Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
title_full_unstemmed Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
title_short Identification of CD38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
title_sort identification of cd38 as a potential biomarker in skin cutaneous melanoma using bioinformatics analysis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7405635/
https://www.ncbi.nlm.nih.gov/pubmed/32774485
http://dx.doi.org/10.3892/ol.2020.11873
work_keys_str_mv AT wangxianwang identificationofcd38asapotentialbiomarkerinskincutaneousmelanomausingbioinformaticsanalysis
AT wangpengli identificationofcd38asapotentialbiomarkerinskincutaneousmelanomausingbioinformaticsanalysis
AT gelei identificationofcd38asapotentialbiomarkerinskincutaneousmelanomausingbioinformaticsanalysis
AT wangjuan identificationofcd38asapotentialbiomarkerinskincutaneousmelanomausingbioinformaticsanalysis
AT naqvisyedmanzarabbasshah identificationofcd38asapotentialbiomarkerinskincutaneousmelanomausingbioinformaticsanalysis
AT hushujuan identificationofcd38asapotentialbiomarkerinskincutaneousmelanomausingbioinformaticsanalysis