Clinical and Molecular Comparative Study of Colorectal Cancer Based on Age-of-onset and Tumor Location: Two Main Criteria for Subclassifying Colorectal Cancer

• Published in: International journal of molecular sciences Vol. 20; no. 4; p. 968
• Main Authors: Álvaro, Edurne, Cano, Juana M, García, Juan L, Brandáriz, Lorena, Olmedillas-López, Susana, Arriba, María, Rueda, Daniel, Rodríguez, Yolanda, Cañete, Ángel, Arribas, Julia, Inglada-Pérez, Lucía, Pérez, Jessica, Gómez, Carlos, García-Arranz, Mariano, García-Olmo, Damián, Goel, Ajay, Urioste, Miguel, González-Sarmiento, Rogelio, Perea, José
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 22.02.2019; MDPI
• Subjects: Age; chromosomal instability; Chromosomes; Colon; Colorectal cancer; Colorectal carcinoma; Comparative studies; CpG island methylator phenotype; early-onset colorectal cancer; late-onset colorectal cancer; microsatellite instability; Mutation; Polyps; Rectum; tumor location; Tumors; late-onset colorectal cancer; microsatellite instability; CpG island methylator phenotype; chromosomal instability; tumor location; early-onset colorectal cancer
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms20040968

Our aim was to characterize and validate that the location and age of onset of the tumor are both important criteria to classify colorectal cancer (CRC). We analyzed clinical and molecular characteristics of early-onset CRC (EOCRC) and late-onset CRC (LOCRC), and we compared each tumor location between both ages-of-onset. In right-sided colon tumors, early-onset cases showed extensive Lynch syndrome (LS) features, with a relatively low frequency of chromosomal instability (CIN), but a high CpG island methylation phenotype. Nevertheless, late-onset cases showed predominantly sporadic features and microsatellite instability cases due to mutations. In left colon cancers, the most reliable clinical features were the tendency to develop polyps as well as multiple primary CRC associated with the late-onset subset. Apart from the higher degree of CIN in left-sided early-onset cancers, differential copy number alterations were also observed. Differences among rectal cancers showed that early-onset rectal cancers were diagnosed at later stages, had less association with polyps, and more than half of them were associated with a familial LS component. Stratifying CRC according to both location and age-of-onset criteria is meaningful, not only because it correlates the resulting categories with certain molecular bases, but with the confirmation across larger studies, new therapeutical algorithms could be defined according to this subclassification.