Network Mapping of Molecular Biomarkers Influencing Radiation Response in Rectal Cancer.


Journal

Clinical colorectal cancer
ISSN: 1938-0674
Titre abrégé: Clin Colorectal Cancer
Pays: United States
ID NLM: 101120693

Informations de publication

Date de publication:
06 2019
Historique:
received: 19 06 2018
revised: 12 11 2018
accepted: 23 01 2019
pubmed: 1 4 2019
medline: 3 4 2020
entrez: 1 4 2019
Statut: ppublish

Résumé

Preoperative radiotherapy (RT) plays an important role in the management of locally advanced rectal cancer (RC). Tumor regression after RT shows marked variability, and robust molecular methods are needed to help predict likely response. The aim of this study was to review the current published literature and use Gene Ontology (GO) analysis to define key molecular biomarkers governing radiation response in RC. A systematic review of electronic bibliographic databases (Medline, Embase) was performed for original articles published between 2000 and 2015. Biomarkers were then classified according to biological function and incorporated into a hierarchical GO tree. Both significant and nonsignificant results were included in the analysis. Significance was binarized on the basis of univariate and multivariate statistics. Significance scores were calculated for each biological domain (or node), and a direct acyclic graph was generated for intuitive mapping of biological pathways and markers involved in RC radiation response. Seventy-two individual biomarkers across 74 studies were identified. On highest-order classification, molecular biomarkers falling within the domains of response to stress, cellular metabolism, and pathways inhibiting apoptosis were found to be the most influential in predicting radiosensitivity. Homogenizing biomarker data from original articles using controlled GO terminology demonstrated that cellular mechanisms of response to RT in RC-in particular the metabolic response to RT-may hold promise in developing radiotherapeutic biomarkers to help predict, and in the future modulate, radiation response.

Identifiants

pubmed: 30928329
pii: S1533-0028(18)30291-3
doi: 10.1016/j.clcc.2019.01.004
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e210-e222

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
Pays : United Kingdom

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Liam Poynter (L)

Department of Surgery & Cancer, Imperial College London, London, UK.

Dieter Galea (D)

Computational & Systems Medicine, Imperial College London, London, UK.

Kirill Veselkov (K)

Computational & Systems Medicine, Imperial College London, London, UK.

Alexander Mirnezami (A)

Department of Surgical Oncology, University of Southampton, Southampton, UK.

James Kinross (J)

Department of Surgery & Cancer, Imperial College London, London, UK.

Jeremy Nicholson (J)

Computational & Systems Medicine, Imperial College London, London, UK.

Zoltán Takáts (Z)

Computational & Systems Medicine, Imperial College London, London, UK.

Ara Darzi (A)

Department of Surgery & Cancer, Imperial College London, London, UK.

Reza Mirnezami (R)

Department of Surgery & Cancer, Imperial College London, London, UK; St Mark's Hospital and Academic Institute, Harrow, London, UK. Electronic address: r.mirnezami@imperial.ac.uk.

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Classifications MeSH