Perea José, Cano Juana M, Rueda Daniel, García Juan L, Inglada Lucía, Osorio Irene, Arriba María, Pérez Jessica, Gaspar Miriam, Fernández-Miguel Tamara, Rodríguez Yolanda, Benítez Javier, González-Sarmiento Rogelio, Urioste Miguel
Department of Surgery, Hospital Universitario 12 de Octubre Madrid, Spain ; Digestive Cancer Research Group, Hospital 12 de Octubre Research Institute Madrid, Spain.
Department of Medical Oncology, Ciudad Real General Hospital Ciudad Real, Spain.
Am J Cancer Res. 2015 Jun 15;5(7):2308-13. eCollection 2015.
Early-onset Colorectal Cancer (ECRC) represents a significant and increasing proportion of Colorectal Cancer (CRC), but it is a heterogeneous entity that probably encompasses specific subclasses. On the premise that the carcinogenetic mechanism and progression of CRC may differ with location, we analyzed molecular and clinical characteristics of ECRC according to tumor location in order to identify more homogeneous subgroups of CRC. Right-sided ECRC is a subset in which most Lynch Syndrome cases are found, with earlier stages at diagnosis and better prognosis. At this location the CpG Island Methylator Phenotype (CIMP) is predominant and Chromosomal Instability (CI) is rare. Left-sided ECRC appears as a transitional or intermediate location, except for CI tumors, that seem to predominate at this location. Finally, rectal ECRC shows Microsatellite Stability, CIMP low-0 and low CI - with recurrent altered chromosomal regions in common with left-sided ECRC-, possibly in relation with Microsatellite And Chromosomal Stable tumors, but with an unexpected familial component and worse prognosis. All this suggest that the molecular basis of ECRC varies with tumor location, which could affect the clinical management of patients.
早发性结直肠癌(ECRC)在结直肠癌(CRC)中所占比例显著且呈上升趋势,但它是一个异质性实体,可能包含特定的亚类。基于CRC的致癌机制和进展可能因部位而异这一前提,我们根据肿瘤部位分析了ECRC的分子和临床特征,以确定CRC更具同质性的亚组。右侧ECRC是一个亚组,其中大多数林奇综合征病例在此被发现,诊断时分期较早且预后较好。在这个部位,CpG岛甲基化表型(CIMP)占主导,染色体不稳定(CI)罕见。左侧ECRC表现为一个过渡或中间部位,除了CI肿瘤似乎在该部位占主导外。最后,直肠ECRC表现为微卫星稳定、CIMP低和CI低,与左侧ECRC有共同的反复改变的染色体区域,可能与微卫星和染色体稳定肿瘤有关,但有意外的家族成分且预后较差。所有这些表明,ECRC的分子基础因肿瘤部位而异,这可能会影响患者的临床管理。