Personalised medicine based on host genetics and microbiota applied to colorectal cancer.

Biomarker Colorectal cancer (CRC) Diagnostic Gut microbiota Host genetics Precision medicine Predictive Prognostic Treatment

Journal

Advances in genetics
ISSN: 0065-2660
Titre abrégé: Adv Genet
Pays: United States
ID NLM: 0370421

Informations de publication

Date de publication:
2024
Historique:
medline: 14 10 2024
pubmed: 14 10 2024
entrez: 13 10 2024
Statut: ppublish

Résumé

Colorectal cancer (CRC) ranks second in incidence and third in cancer mortality worldwide. This situation, together with the understanding of the heterogeneity of the disease, has highlighted the need to develop a more individualised approach to its prevention, diagnosis and treatment through personalised medicine. This approach aims to stratify patients according to risk, predict disease progression and determine the most appropriate treatment. It is essential to identify patients who may respond adequately to treatment and those who may be resistant to treatment to avoid unnecessary therapies and minimise adverse side effects. Current research is focused on identifying biomarkers such as specific mutated genes, the type of mutations and molecular profiles critical for the individualisation of CRC diagnosis, prognosis and treatment guidance. In addition, the study of the intestinal microbiota as biomarkers is being incorporated due to the growing scientific evidence supporting its influence on this disease. This article comprehensively addresses the use of current and emerging diagnostic, prognostic and predictive biomarkers in precision medicine against CRC. The effects of host genetics and gut microbiota composition on new approaches to treating this disease are discussed. How the gut microbiota could mitigate the side effects of treatment is reviewed. In addition, strategies to modulate the gut microbiota, such as dietary interventions, antibiotics, and transplantation of faecal microbiota and phages, are discussed to improve CRC prevention and treatment. These findings provide a solid foundation for future research and improving the care of CRC patients.

Identifiants

pubmed: 39396842
pii: S0065-2660(24)00025-7
doi: 10.1016/bs.adgen.2024.08.004
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

411-485

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Adriana González (A)

Hologenomics Research Group, Department of Genetics, Physical Anthropology, and Animal Physiology, University of the Basque Country, Spain.

Iker Badiola (I)

Department of Cell Biology and Histology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.

Asier Fullaondo (A)

Hologenomics Research Group, Department of Genetics, Physical Anthropology, and Animal Physiology, University of the Basque Country, Spain.

Javier Rodríguez (J)

Department of Oncology, Clínica Universidad de Navarra, Spain.

Adrian Odriozola (A)

Hologenomics Research Group, Department of Genetics, Physical Anthropology, and Animal Physiology, University of the Basque Country, Spain. Electronic address: adrian.odriozola@ehu.eus.

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Classifications MeSH