Cancer epigenetics: Moving forward
Defects in chromatin modifiers and remodelers have been described both for hematological and solid malignancies, corroborating and strengthening the role of epigenetic aberrations in the etiology of cancer. Furthermore, epigenetic marks-DNA methylation, histone modifications, chromatin remodeling, a...
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| Vydané v: | PLoS genetics Ročník 14; číslo 6; s. e1007362 |
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| Hlavní autori: | , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
United States
Public Library of Science
07.06.2018
Public Library of Science (PLoS) |
| Predmet: | |
| ISSN: | 1553-7404, 1553-7390, 1553-7404 |
| On-line prístup: | Získať plný text |
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| Abstract | Defects in chromatin modifiers and remodelers have been described both for hematological and solid malignancies, corroborating and strengthening the role of epigenetic aberrations in the etiology of cancer. Furthermore, epigenetic marks-DNA methylation, histone modifications, chromatin remodeling, and microRNA-can be considered potential markers of cancer development and progression. Here, we review whether altered epigenetic landscapes are merely a consequence of chromatin modifier/remodeler aberrations or a hallmark of cancer etiology. We critically evaluate current knowledge on causal epigenetic aberrations and examine to what extent the prioritization of (epi)genetic deregulations can be assessed in cancer as some type of genetic lesion characterizing solid cancer progression. We also discuss the multiple challenges in developing compounds targeting epigenetic enzymes (named epidrugs) for epigenetic-based therapies. The implementation of acquired knowledge of epigenetic biomarkers for patient stratification, together with the development of next-generation epidrugs and predictive models, will take our understanding and use of cancer epigenetics in diagnosis, prognosis, and treatment of cancer patients to a new level. |
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| AbstractList | Defects in chromatin modifiers and remodelers have been described both for hematological and solid malignancies, corroborating and strengthening the role of epigenetic aberrations in the etiology of cancer. Furthermore, epigenetic marks—DNA methylation, histone modifications, chromatin remodeling, and microRNA—can be considered potential markers of cancer development and progression. Here, we review whether altered epigenetic landscapes are merely a consequence of chromatin modifier/remodeler aberrations or a hallmark of cancer etiology. We critically evaluate current knowledge on causal epigenetic aberrations and examine to what extent the prioritization of (epi)genetic deregulations can be assessed in cancer as some type of genetic lesion characterizing solid cancer progression. We also discuss the multiple challenges in developing compounds targeting epigenetic enzymes (named epidrugs) for epigenetic-based therapies. The implementation of acquired knowledge of epigenetic biomarkers for patient stratification, together with the development of next-generation epidrugs and predictive models, will take our understanding and use of cancer epigenetics in diagnosis, prognosis, and treatment of cancer patients to a new level. Defects in chromatin modifiers and remodelers have been described both for hematological and solid malignancies, corroborating and strengthening the role of epigenetic aberrations in the etiology of cancer. Furthermore, epigenetic marks-DNA methylation, histone modifications, chromatin remodeling, and microRNA-can be considered potential markers of cancer development and progression. Here, we review whether altered epigenetic landscapes are merely a consequence of chromatin modifier/remodeler aberrations or a hallmark of cancer etiology. We critically evaluate current knowledge on causal epigenetic aberrations and examine to what extent the prioritization of (epi)genetic deregulations can be assessed in cancer as some type of genetic lesion characterizing solid cancer progression. We also discuss the multiple challenges in developing compounds targeting epigenetic enzymes (named epidrugs) for epigenetic-based therapies. The implementation of acquired knowledge of epigenetic biomarkers for patient stratification, together with the development of next-generation epidrugs and predictive models, will take our understanding and use of cancer epigenetics in diagnosis, prognosis, and treatment of cancer patients to a new level.Defects in chromatin modifiers and remodelers have been described both for hematological and solid malignancies, corroborating and strengthening the role of epigenetic aberrations in the etiology of cancer. Furthermore, epigenetic marks-DNA methylation, histone modifications, chromatin remodeling, and microRNA-can be considered potential markers of cancer development and progression. Here, we review whether altered epigenetic landscapes are merely a consequence of chromatin modifier/remodeler aberrations or a hallmark of cancer etiology. We critically evaluate current knowledge on causal epigenetic aberrations and examine to what extent the prioritization of (epi)genetic deregulations can be assessed in cancer as some type of genetic lesion characterizing solid cancer progression. We also discuss the multiple challenges in developing compounds targeting epigenetic enzymes (named epidrugs) for epigenetic-based therapies. The implementation of acquired knowledge of epigenetic biomarkers for patient stratification, together with the development of next-generation epidrugs and predictive models, will take our understanding and use of cancer epigenetics in diagnosis, prognosis, and treatment of cancer patients to a new level. |
| Audience | Academic |
| Author | Nebbioso, Angela Dell’Aversana, Carmela Altucci, Lucia Tambaro, Francesco Paolo |
| AuthorAffiliation | Albert Einstein College of Medicine, UNITED STATES 1 Dipartimento di Medicina di Precisione, Università degli Studi della Campania “L. Vanvitelli,” Napoli, Italy 2 Struttura Semplice Dipartimentale Trapianto di Midollo Osseo-Azienda Ospedialiera di Rilievo Nazionale, Santobono-Pausilipon, Napoli, Italy |
| AuthorAffiliation_xml | – name: 1 Dipartimento di Medicina di Precisione, Università degli Studi della Campania “L. Vanvitelli,” Napoli, Italy – name: Albert Einstein College of Medicine, UNITED STATES – name: 2 Struttura Semplice Dipartimentale Trapianto di Midollo Osseo-Azienda Ospedialiera di Rilievo Nazionale, Santobono-Pausilipon, Napoli, Italy |
| Author_xml | – sequence: 1 givenname: Angela orcidid: 0000-0001-5374-3527 surname: Nebbioso fullname: Nebbioso, Angela – sequence: 2 givenname: Francesco Paolo surname: Tambaro fullname: Tambaro, Francesco Paolo – sequence: 3 givenname: Carmela surname: Dell’Aversana fullname: Dell’Aversana, Carmela – sequence: 4 givenname: Lucia orcidid: 0000-0002-7312-5387 surname: Altucci fullname: Altucci, Lucia |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29879107$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Biology Biology and life sciences Biomarkers, Tumor - genetics Breast cancer Cancer Cancer genetics Cancer research Cancer therapies Chromatin Chromatin Assembly and Disassembly - genetics Chromatin remodeling Consortia Deoxyribonucleic acid Disease Disease Progression DNA DNA methylation DNA Methylation - genetics Enzyme Inhibitors - pharmacology Enzyme Inhibitors - therapeutic use Enzymes - genetics Enzymes - metabolism Epigenesis, Genetic - drug effects Epigenetic inheritance Epigenetics Epigenomics - methods Etiology Forecasts and trends Gene expression Gene Expression Regulation, Neoplastic Genetic research Genomes Histone Code - genetics Humans Leukemia Medicine and Health Sciences MicroRNAs - genetics miRNA Molecular Targeted Therapy - methods Mutation Neoplasms - diagnosis Neoplasms - drug therapy Neoplasms - genetics Patients Prognosis Review Transcription factors Tumorigenesis |
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| Title | Cancer epigenetics: Moving forward |
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