The Role of Epigenetics in the Progression of Clear Cell Renal Cell Carcinoma and the Basis for Future Epigenetic Treatments
Clear cell renal cell carcinoma (ccRCC) is curable when diagnosed at an early stage, but when disease is non-confined it is the urologic cancer with worst prognosis. Antiangiogenic treatment and immune checkpoint inhibition therapy constitute a very promising combined therapy for advanced and metast...
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Veröffentlicht in: | Cancers 2021-04, Vol.13 (9), p.2071 |
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description | Clear cell renal cell carcinoma (ccRCC) is curable when diagnosed at an early stage, but when disease is non-confined it is the urologic cancer with worst prognosis. Antiangiogenic treatment and immune checkpoint inhibition therapy constitute a very promising combined therapy for advanced and metastatic disease. Many exploratory studies have identified epigenetic markers based on DNA methylation, histone modification, and ncRNA expression that epigenetically regulate gene expression in ccRCC. Additionally, epigenetic modifiers genes have been proposed as promising biomarkers for ccRCC. We review and discuss the current understanding of how epigenetic changes determine the main molecular pathways of ccRCC initiation and progression, and also its clinical implications. Despite the extensive research performed, candidate epigenetic biomarkers are not used in clinical practice for several reasons. However, the accumulated body of evidence of developing epigenetically-based biomarkers will likely allow the identification of ccRCC at a higher risk of progression. That will facilitate the establishment of firmer therapeutic decisions in a changing landscape and also monitor active surveillance in the aging population. What is more, a better knowledge of the activities of chromatin modifiers may serve to develop new therapeutic opportunities. Interesting clinical trials on epigenetic treatments for ccRCC associated with well established antiangiogenic treatments and immune checkpoint inhibitors are revisited. |
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Antiangiogenic treatment and immune checkpoint inhibition therapy constitute a very promising combined therapy for advanced and metastatic disease. Many exploratory studies have identified epigenetic markers based on DNA methylation, histone modification, and ncRNA expression that epigenetically regulate gene expression in ccRCC. Additionally, epigenetic modifiers genes have been proposed as promising biomarkers for ccRCC. We review and discuss the current understanding of how epigenetic changes determine the main molecular pathways of ccRCC initiation and progression, and also its clinical implications. Despite the extensive research performed, candidate epigenetic biomarkers are not used in clinical practice for several reasons. However, the accumulated body of evidence of developing epigenetically-based biomarkers will likely allow the identification of ccRCC at a higher risk of progression. That will facilitate the establishment of firmer therapeutic decisions in a changing landscape and also monitor active surveillance in the aging population. What is more, a better knowledge of the activities of chromatin modifiers may serve to develop new therapeutic opportunities. Interesting clinical trials on epigenetic treatments for ccRCC associated with well established antiangiogenic treatments and immune checkpoint inhibitors are revisited.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13092071</identifier><identifier>PMID: 33922974</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aging ; Apoptosis ; Biomarkers ; Cancer therapies ; Chromatin ; Clear cell-type renal cell carcinoma ; Clinical trials ; DNA methylation ; Epigenetics ; Gene expression ; Histones ; Immune checkpoint inhibitors ; Immunotherapy ; Kidney cancer ; Kinases ; Malignancy ; Medical prognosis ; Metastases ; Metastasis ; MicroRNAs ; Non-coding RNA ; Prognosis ; Proteins ; Review ; Tumors</subject><ispartof>Cancers, 2021-04, Vol.13 (9), p.2071</ispartof><rights>2021 by the authors. 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/). 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Antiangiogenic treatment and immune checkpoint inhibition therapy constitute a very promising combined therapy for advanced and metastatic disease. Many exploratory studies have identified epigenetic markers based on DNA methylation, histone modification, and ncRNA expression that epigenetically regulate gene expression in ccRCC. Additionally, epigenetic modifiers genes have been proposed as promising biomarkers for ccRCC. We review and discuss the current understanding of how epigenetic changes determine the main molecular pathways of ccRCC initiation and progression, and also its clinical implications. Despite the extensive research performed, candidate epigenetic biomarkers are not used in clinical practice for several reasons. However, the accumulated body of evidence of developing epigenetically-based biomarkers will likely allow the identification of ccRCC at a higher risk of progression. That will facilitate the establishment of firmer therapeutic decisions in a changing landscape and also monitor active surveillance in the aging population. What is more, a better knowledge of the activities of chromatin modifiers may serve to develop new therapeutic opportunities. Interesting clinical trials on epigenetic treatments for ccRCC associated with well established antiangiogenic treatments and immune checkpoint inhibitors are revisited.</description><subject>Aging</subject><subject>Apoptosis</subject><subject>Biomarkers</subject><subject>Cancer therapies</subject><subject>Chromatin</subject><subject>Clear cell-type renal cell carcinoma</subject><subject>Clinical trials</subject><subject>DNA methylation</subject><subject>Epigenetics</subject><subject>Gene expression</subject><subject>Histones</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Kidney cancer</subject><subject>Kinases</subject><subject>Malignancy</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>MicroRNAs</subject><subject>Non-coding RNA</subject><subject>Prognosis</subject><subject>Proteins</subject><subject>Review</subject><subject>Tumors</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkUlLBDEQhYMoKurZmwS8eBnN2stF0MYNBEXGc0jHyhjpTsakWxD88WYcldFcquB99ajKQ2ifkmPOa3JitDcQE-WkZqSka2g7FzYpilqsr_RbaC-lF5If57Qsyk20lccZq0uxjT6mz4AfQgc4WHwxdzPwMDiTsPN4yNJ9DLMIKbngF0TTgY64ga7DD-B1t2wbHY3zoddY-6evsXOdXMI2RHw5DmOEFWs8jaCHHvyQdtGG1V2Cve-6gx4vL6bN9eT27uqmObudGMHoMGG6FNKaSnJDC120hRWGU9lWtTSCFtS0bSWl4RYIUF6IJwOm5Lrl3FbMCsl30OnSdz62PWTZD1F3ah5dr-O7Ctqpv4p3z2oW3lRFGedyYXD0bRDD6whpUL1LJp-uPYQxKSYZqcqKCJHRw3_oSxhj_qovqmJSSkYzdbKkTAwpRbC_y1CiFuGqf-HmiYPVG375nyj5J8l1ofQ</recordid><startdate>20210425</startdate><enddate>20210425</enddate><creator>Angulo, Javier C</creator><creator>Manini, Claudia</creator><creator>López, Jose I</creator><creator>Pueyo, Angel</creator><creator>Colás, Begoña</creator><creator>Ropero, Santiago</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1735-8792</orcidid><orcidid>https://orcid.org/0000-0003-0842-5348</orcidid></search><sort><creationdate>20210425</creationdate><title>The Role of Epigenetics in the Progression of Clear Cell Renal Cell Carcinoma and the Basis for Future Epigenetic Treatments</title><author>Angulo, Javier C ; 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Antiangiogenic treatment and immune checkpoint inhibition therapy constitute a very promising combined therapy for advanced and metastatic disease. Many exploratory studies have identified epigenetic markers based on DNA methylation, histone modification, and ncRNA expression that epigenetically regulate gene expression in ccRCC. Additionally, epigenetic modifiers genes have been proposed as promising biomarkers for ccRCC. We review and discuss the current understanding of how epigenetic changes determine the main molecular pathways of ccRCC initiation and progression, and also its clinical implications. Despite the extensive research performed, candidate epigenetic biomarkers are not used in clinical practice for several reasons. However, the accumulated body of evidence of developing epigenetically-based biomarkers will likely allow the identification of ccRCC at a higher risk of progression. 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subjects | Aging Apoptosis Biomarkers Cancer therapies Chromatin Clear cell-type renal cell carcinoma Clinical trials DNA methylation Epigenetics Gene expression Histones Immune checkpoint inhibitors Immunotherapy Kidney cancer Kinases Malignancy Medical prognosis Metastases Metastasis MicroRNAs Non-coding RNA Prognosis Proteins Review Tumors |
title | The Role of Epigenetics in the Progression of Clear Cell Renal Cell Carcinoma and the Basis for Future Epigenetic Treatments |
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