Familial colorectal cancer type X syndrome: two distinct molecular entities?

• Published in: Familial cancer Vol. 10; no. 4; pp. 623 - 631
• Main Authors: Francisco, Inês, Albuquerque, Cristina, Lage, Pedro, Belo, Hélio, Vitoriano, Inês, Filipe, Bruno, Claro, Isabel, Ferreira, Sara, Rodrigues, Paula, Chaves, Paula, Leitão, Carlos Nobre, Pereira, António Dias
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.12.2011; Springer Nature B.V
• Subjects: Adenoma - genetics; Adult; Aged; Biomedical and Life Sciences; Biomedicine; Cancer Research; Carcinoma - genetics; Colorectal cancer; Colorectal Neoplasms, Hereditary Nonpolyposis - classification; Colorectal Neoplasms, Hereditary Nonpolyposis - genetics; DNA Methylation; DNA Mismatch Repair - genetics; Epidemiology; Female; Genes, Tumor Suppressor; Human Genetics; Humans; Loss of Heterozygosity; Male; Middle Aged; Neoplastic Syndromes, Hereditary - classification; Neoplastic Syndromes, Hereditary - genetics; Nuclear Proteins - genetics; Portugal; Promoter Regions, Genetic - genetics; Portugal; Colorectal cancer; Familial colorectal cancer type X; Lynch syndrome
• ISSN: 1389-9600; 1573-7292
• DOI: 10.1007/s10689-011-9473-7

In a fraction of families fulfilling the Amsterdam criteria for hereditary non-polyposis colorectal cancer, colorectal cancers are microsatellite stable and DNA mismatch repair gene (MMR) mutations are not found. These families were designated as familial colorectal cancer type X (FCCTX). We aimed to characterise a group of FCCTX families defined by the Amsterdam criteria and MSS tumours at clinical and molecular level. Twenty-four tumours from 15 FCCTX families were analysed for loss of known tumour suppressor gene (TSG) loci ( APC , TP53 , SMAD4 and DCC ), MGMT and MMR genes promoter methylation, and also APC and KRAS somatic mutations. FCCTX families presented specific clinical features: absence of endometrial tumours, high adenoma/carcinoma ratio (1.91) and prevalence of rectal cancers (13/27, 48%). New molecular features were found: the majority of FCCTX tumours (13/18; 72%) presented TSG loss. TSG loss positive tumours presented frequent APC and KRAS somatic mutations and MGMT methylation [10/13 (77%), 7/13 (54%) and 6/11 (54%), respectively]. In TSG loss negative tumours (5/18; 28%), the same molecular events were found in 2/5 (40%), 2/5 (40%) and 1/3 (33%) tumours, respectively. Transition mutations in KRAS were more frequent among MGMT methylated tumours than in unmethylated [5/8 (63%) vs. 1/10 (10%), P  = 0.03]. Although sharing similar clinical features, at least two different molecular entities should exist among FCCTX families, one whose tumours present frequent TSG loss, APC and KRAS somatic mutations, and MGMT promoter methylation, and a second, lesser predominant, with no evidence of TSG loss and rarely presenting promoter methylation.