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CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications

Target identification is a crucial process in drug development, aiming to identify key proteins, genes, and signal pathways involved in disease progression and their relevance in potential therapeutic interventions. While C-C chemokine receptor 8 (CCR8) has been investigated as a candidate anti-canc...

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Autores principales: Kim, Nari, Kim, Mi-Hyun, Pyo, Junhee, Lee, Soo-Min, Jang, Ji-Sung, Lee, Do-Wan, Kim, Kyung Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669377/
https://www.ncbi.nlm.nih.gov/pubmed/38001911
http://dx.doi.org/10.3390/biomedicines11112910
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author Kim, Nari
Kim, Mi-Hyun
Pyo, Junhee
Lee, Soo-Min
Jang, Ji-Sung
Lee, Do-Wan
Kim, Kyung Won
author_facet Kim, Nari
Kim, Mi-Hyun
Pyo, Junhee
Lee, Soo-Min
Jang, Ji-Sung
Lee, Do-Wan
Kim, Kyung Won
author_sort Kim, Nari
collection PubMed
description Target identification is a crucial process in drug development, aiming to identify key proteins, genes, and signal pathways involved in disease progression and their relevance in potential therapeutic interventions. While C-C chemokine receptor 8 (CCR8) has been investigated as a candidate anti-cancer target, comprehensive multi-omics analyzes across various indications are limited. In this study, we conducted an extensive bioinformatics analysis integrating genomics, proteomics, and transcriptomics data to establish CCR8 as a promising anti-cancer drug target. Our approach encompassed data collection from diverse knowledge resources, gene function analysis, differential gene expression profiling, immune cell infiltration assessment, and strategic prioritization of target indications. Our findings revealed strong correlations between CCR8 and specific cancers, notably Breast Invasive Carcinoma (BRCA), Colon Adenocarcinoma (COAD), Head and Neck Squamous Cell Carcinoma (HNSC), Rectum adenocarcinoma (READ), Stomach adenocarcinoma (STAD), and Thyroid carcinoma (THCA). This research advances our understanding of CCR8 as a potential target for anti-cancer drug development, bridging the gap between molecular insights and creating opportunities for personalized treatment of solid tumors.
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spelling pubmed-106693772023-10-27 CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications Kim, Nari Kim, Mi-Hyun Pyo, Junhee Lee, Soo-Min Jang, Ji-Sung Lee, Do-Wan Kim, Kyung Won Biomedicines Article Target identification is a crucial process in drug development, aiming to identify key proteins, genes, and signal pathways involved in disease progression and their relevance in potential therapeutic interventions. While C-C chemokine receptor 8 (CCR8) has been investigated as a candidate anti-cancer target, comprehensive multi-omics analyzes across various indications are limited. In this study, we conducted an extensive bioinformatics analysis integrating genomics, proteomics, and transcriptomics data to establish CCR8 as a promising anti-cancer drug target. Our approach encompassed data collection from diverse knowledge resources, gene function analysis, differential gene expression profiling, immune cell infiltration assessment, and strategic prioritization of target indications. Our findings revealed strong correlations between CCR8 and specific cancers, notably Breast Invasive Carcinoma (BRCA), Colon Adenocarcinoma (COAD), Head and Neck Squamous Cell Carcinoma (HNSC), Rectum adenocarcinoma (READ), Stomach adenocarcinoma (STAD), and Thyroid carcinoma (THCA). This research advances our understanding of CCR8 as a potential target for anti-cancer drug development, bridging the gap between molecular insights and creating opportunities for personalized treatment of solid tumors. MDPI 2023-10-27 /pmc/articles/PMC10669377/ /pubmed/38001911 http://dx.doi.org/10.3390/biomedicines11112910 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Nari
Kim, Mi-Hyun
Pyo, Junhee
Lee, Soo-Min
Jang, Ji-Sung
Lee, Do-Wan
Kim, Kyung Won
CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications
title CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications
title_full CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications
title_fullStr CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications
title_full_unstemmed CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications
title_short CCR8 as a Therapeutic Novel Target: Omics-Integrated Comprehensive Analysis for Systematically Prioritizing Indications
title_sort ccr8 as a therapeutic novel target: omics-integrated comprehensive analysis for systematically prioritizing indications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669377/
https://www.ncbi.nlm.nih.gov/pubmed/38001911
http://dx.doi.org/10.3390/biomedicines11112910
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