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Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma
BACKGROUND: Skin cutaneous melanoma (SKCM) is one of the most aggressive malignancies with high invasiveness. Chromobox (CBX) family are involved in the regulation of the tumorigenesis, progression, invasion, and apoptosis of many malignancies. METHODS: The clinical significance and prognostic value...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755763/ https://www.ncbi.nlm.nih.gov/pubmed/32860274 http://dx.doi.org/10.1002/jcla.23537 |
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author | Li, Ding Liu, YiRan Hao, Shuai Chen, Bo Li, AnHai |
author_facet | Li, Ding Liu, YiRan Hao, Shuai Chen, Bo Li, AnHai |
author_sort | Li, Ding |
collection | PubMed |
description | BACKGROUND: Skin cutaneous melanoma (SKCM) is one of the most aggressive malignancies with high invasiveness. Chromobox (CBX) family are involved in the regulation of the tumorigenesis, progression, invasion, and apoptosis of many malignancies. METHODS: The clinical significance and prognostic value of CBX family in SKCM were analyzed via a series of databases, including ONCOMINE, GEPIA, UALCAN, TIMER, GSCALite, DAVID 6.8, GeneMANIA, and LinkedOmics. RESULTS: We found that the level of CBX2, CBX3, CBX5, and CBX6 was upregulated while the level of CBX7 and CBX8 was downregulated in tumor tissues in SKCM. Moreover, the mRNA expression of CBX1 and CBX2 was significantly associated with the pathological stage in SKCM. Prognosis analysis revealed that SKCM patients with high CBX5 level and low CBX7 level had a poor prognosis. Immune infiltrations analysis revealed that the expression of CBX family was associated with the abundance of certain immune cells in SKCM. We also found that CBX family were associated with the activation of cell cycle pathway and DNA damage response, and the inhibition of apoptosis pathway. Moreover, enrichment analysis revealed that CBX family and correlated genes were enriched in chromatin modification, PcG protein complex, transcription coactivator activity, protein binding, and RNA splicing. Several Kinase targets (ATM, CDK1, and PLK1) and miRNA targets (MIR‐331, MIR‐296, and MIR‐496) of CBX family were also identified. CONCLUSION: Our study may uncover CBX family–associated molecular mechanisms involved in the tumorigenesis and progression of SKCM and provide additional choice for the prognosis and therapy biomarker for SKCM. |
format | Online Article Text |
id | pubmed-7755763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77557632020-12-23 Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma Li, Ding Liu, YiRan Hao, Shuai Chen, Bo Li, AnHai J Clin Lab Anal Research Articles BACKGROUND: Skin cutaneous melanoma (SKCM) is one of the most aggressive malignancies with high invasiveness. Chromobox (CBX) family are involved in the regulation of the tumorigenesis, progression, invasion, and apoptosis of many malignancies. METHODS: The clinical significance and prognostic value of CBX family in SKCM were analyzed via a series of databases, including ONCOMINE, GEPIA, UALCAN, TIMER, GSCALite, DAVID 6.8, GeneMANIA, and LinkedOmics. RESULTS: We found that the level of CBX2, CBX3, CBX5, and CBX6 was upregulated while the level of CBX7 and CBX8 was downregulated in tumor tissues in SKCM. Moreover, the mRNA expression of CBX1 and CBX2 was significantly associated with the pathological stage in SKCM. Prognosis analysis revealed that SKCM patients with high CBX5 level and low CBX7 level had a poor prognosis. Immune infiltrations analysis revealed that the expression of CBX family was associated with the abundance of certain immune cells in SKCM. We also found that CBX family were associated with the activation of cell cycle pathway and DNA damage response, and the inhibition of apoptosis pathway. Moreover, enrichment analysis revealed that CBX family and correlated genes were enriched in chromatin modification, PcG protein complex, transcription coactivator activity, protein binding, and RNA splicing. Several Kinase targets (ATM, CDK1, and PLK1) and miRNA targets (MIR‐331, MIR‐296, and MIR‐496) of CBX family were also identified. CONCLUSION: Our study may uncover CBX family–associated molecular mechanisms involved in the tumorigenesis and progression of SKCM and provide additional choice for the prognosis and therapy biomarker for SKCM. John Wiley and Sons Inc. 2020-08-28 /pmc/articles/PMC7755763/ /pubmed/32860274 http://dx.doi.org/10.1002/jcla.23537 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Li, Ding Liu, YiRan Hao, Shuai Chen, Bo Li, AnHai Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma |
title | Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma |
title_full | Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma |
title_fullStr | Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma |
title_full_unstemmed | Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma |
title_short | Mining database for the clinical significance and prognostic value of CBX family in skin cutaneous melanoma |
title_sort | mining database for the clinical significance and prognostic value of cbx family in skin cutaneous melanoma |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755763/ https://www.ncbi.nlm.nih.gov/pubmed/32860274 http://dx.doi.org/10.1002/jcla.23537 |
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