Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome

Ali, O. Hasan; Yurchenko, A. A.; Pavlova, O.; Sartori, A.; Bomze, D.; Higgins, R.; Ring, S. S.; Hartmann, F.; Buehler, D.; Fritzsche, F. R.; Jochum, W.; Navarini, A. A.; Kim, A.; French, L. E.; Dermitzakis, E.; Christiano, A. M.; Hohl, D.; Bickers, D. R.; Nikolaev, S. und Flatz, L. (2020): Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome. In: Journal of the European Academy of Dermatology and Venereology, Bd. 35, Nr. 2: S. 396-402

Abstract

Background: Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant genetic disorder. It is commonly caused by mutations inPTCH1and chiefly characterized by multiple basal cell carcinomas (BCCs) developing prior to the age of 30 years. In rare cases, NBCCS presents with a late onset of BCC development. Objective: To investigate BCC tumorigenesis in two brothers, who showed characteristic features of NBCCS but developed their first BCCs only after the age of 40 years. Two other siblings did not show signs of NBCCS. Results We obtained blood samples from four siblings and nine BCCs from the two brothers with NBCCS. Whole exome sequencing and RNA sequencing revealed loss of heterozygosity (LOH) ofPTCH1in eight out of nine tumours that consistently involved the same haplotype on chromosome 9. This haplotype contained a germinal splice site mutation inPTCH1(NM_001083605:exon9:c.763-6C>A). Analysis of germline DNA confirmed segregation of this mutation with the disease. All BCCs harboured additional somatic loss-of-function (LoF) mutations in the remainingPTCH1allele which are not typically seen in other cases of NBCCS. This suggests a hypomorphic nature of the germinalPTCH1mutation in this family. Furthermore, all BCCs had a similar tumour mutational burden compared to BCCs of unrelated NBCCS patients while harbouring a higher number of damagingPTCH1mutations. Conclusions: Our data suggest that a sequence of three genetic hits leads to the late development of BCCs in two brothers with NBCCS: a hypomorphic germline mutation, followed by somatic LOH and additional mutations that completePTCH1inactivation. These genetic events are in line with the late occurrence of the first BCC and with the higher number of damagingPTCH1mutations compared to usual cases of NBCCS.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• ISSN: 0926-9959
• Sprache: Englisch