Genetic regressive trajectories in colorectal cancer: A new hallmark of oligo-metastatic disease?

Colorectal cancer Genetics Mutations NGS Oligo-metastases

Journal

Translational oncology
ISSN: 1936-5233
Titre abrégé: Transl Oncol
Pays: United States
ID NLM: 101472619

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 14 04 2021
revised: 17 05 2021
accepted: 19 05 2021
pubmed: 26 5 2021
medline: 26 5 2021
entrez: 25 5 2021
Statut: ppublish

Résumé

Colorectal cancer (CRC) originates as consequence of multiple genetic alterations. Some of the involved genes have been extensively studied (APC, TP53, KRAS, SMAD4, PIK3CA, MMR genes) in highly heterogeneous and poly-metastatic cohorts. However, about 10% of metastatic CRC patients presents with an indolent oligo-metastatic disease differently from other patients with poly-metastatic and aggressive clinical course. Which are the genetic dynamics underlying the differences between oligo- and poly-metastatic CRC? The understanding of the genetic trajectories (primary→metastatic) of CRC, in patients selected to represent homogenous clinical models, is crucial to make genotype/phenotype correlations and to identify the molecular events pushing the disease towards an increasing malignant phenotype. This information is crucial to plan innovative therapeutic strategies aimed to reverse or inhibit these phenomena. In the present study, we review the genetic evolution of CRC with the intent to give a developmental perspective on the border line between oligo- and poly-metastatic diseases.

Identifiants

pubmed: 34034007
pii: S1936-5233(21)00123-6
doi: 10.1016/j.tranon.2021.101131
pmc: PMC8144733
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

101131

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

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Auteurs

Alessandro Ottaiano (A)

Istituto Nazionale Tumori di Napoli, IRCCS "G. Pascale", Via M. Semmola, 80131, Naples, Italy. Electronic address: a.ottaiano@istitutotumori.na.it.

Mariachiara Santorsola (M)

Istituto Nazionale Tumori di Napoli, IRCCS "G. Pascale", Via M. Semmola, 80131, Naples, Italy.

Michele Caraglia (M)

Department of Precision Medicine, University of Campania "L. Vanvitelli", Via L. De Crecchio, 7 80138, Naples, Italy; Biogem Scarl, Institute of Genetic Research, Laboratory of Precision and Molecular Oncology, 83031, Ariano Irpino, Italy.

Luisa Circelli (L)

AMES-Centro Polidiagnostico Strumentale, 80013, Casalnuovo di Napoli, Italy.

Valerio Gigantino (V)

Innovalab scarl, Molecular Biology, Centro Direzionale, isola A2, 80143, Naples, Italy.

Gerardo Botti (G)

Istituto Nazionale Tumori di Napoli, IRCCS "G. Pascale", Via M. Semmola, 80131, Naples, Italy.

Guglielmo Nasti (G)

Istituto Nazionale Tumori di Napoli, IRCCS "G. Pascale", Via M. Semmola, 80131, Naples, Italy.

Classifications MeSH