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
Hlavní autori: Nebbioso, Angela, Tambaro, Francesco Paolo, Dell’Aversana, Carmela, Altucci, Lucia
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States Public Library of Science 07.06.2018
Public Library of Science (PLoS)
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ISSN:1553-7404, 1553-7390, 1553-7404
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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.
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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Snippet Defects in chromatin modifiers and remodelers have been described both for hematological and solid malignancies, corroborating and strengthening the role of...
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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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Volume 14
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