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. 2018 Jun;15(6):9413-9419.
doi: 10.3892/ol.2018.8504. Epub 2018 Apr 16.

Screening for susceptibility genes in hereditary non-polyposis colorectal cancer

Affiliations

Screening for susceptibility genes in hereditary non-polyposis colorectal cancer

Li Yu et al. Oncol Lett. 2018 Jun.

Abstract

In the present study, hereditary non-polyposis colorectal cancer (HNPCC) susceptibility genes were screened for using whole exome sequencing in 3 HNPCC patients from 1 family and using single nucleotide polymorphism (SNP) genotyping assays in 96 other colorectal cancer and control samples. Peripheral blood was obtained from 3 HNPCC patients from 1 family; the proband and the proband's brother and cousin. High-throughput sequencing was performed using whole exome capture technology. Sequences were aligned against the HAPMAP, dbSNP130 and 1,000 Genome Project databases. Reported common variations and synonymous mutations were filtered out. Non-synonymous single nucleotide variants in the 3 HNPCC patients were integrated and the candidate genes were identified. Finally, SNP genotyping was performed for the genes in 96 peripheral blood samples. In total, 60.4 Gb of data was retrieved from the 3 HNPCC patients using whole exome capture technology. Subsequently, according to certain screening criteria, 15 candidate genes were identified. Among the 96 samples that had been SNP genotyped, 92 were successfully genotyped for 15 gene loci, while genotyping for HTRA1 failed in 4 sporadic colorectal cancer patient samples. In 12 control subjects and 81 sporadic colorectal cancer patients, genotypes at 13 loci were wild-type, namely DDX20, ZFYVE26, PIK3R3, SLC26A8, ZEB2, TP53INP1, SLC11A1, LRBA, CEBPZ, ETAA1, SEMA3G, IFRD2 and FAT1. The CEP290 genotype was mutant in 1 sporadic colorectal cancer patient and was wild-type in all other subjects. A total of 5 of the 12 control subjects and 30 of the 81 sporadic colorectal cancer patients had a mutant HTRA1 genotype. In all 3 HNPCC patients, the same mutant genotypes were identified at all 15 gene loci. Overall, 13 potential susceptibility genes for HNPCC were identified, namely DDX20, ZFYVE26, PIK3R3, SLC26A8, ZEB2, TP53INP1, SLC11A1, LRBA, CEBPZ, ETAA1, SEMA3G, IFRD2 and FAT1.

Keywords: DDX20; hereditary non-polyposis colorectal cancer; single nucleotide polymorphism; susceptibility gene; whole exome sequencing.

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Figures

Figure 1.
Figure 1.
Pedigree of the HNPCC family. HNPCC, hereditary non-polyposis colorectal cancer.
Figure 2.
Figure 2.
DNA spectrums of (A) CEP290 and (B) HTRA1. b, T-base dissociation absorption peak; d, C-base dissociation absorption peak.
Figure 3.
Figure 3.
DNA spectrums of (A) DDX20 and (B) SLC26A8. a, G-base dissociation absorption peak; b, T-base dissociation absorption peak; c, A-base dissociation absorption peak.

References

    1. Kastrinos F, Stoffel EM. History, genetics, and strategies for cancer prevention in Lynch syndrome. Clin Gastroenterol Hepatol. 2014;12:715–727. doi: 10.1016/j.cgh.2013.06.031. quiz e41-43. - DOI - PMC - PubMed
    1. Watson P, Riley B. The tumor spectrum in the Lynch syndrome. Fam Cancer. 2005;4:245–248. doi: 10.1007/s10689-004-7994-z. - DOI - PubMed
    1. Fishel R, Lescoe MK, Rao MR, Copeland NG, Jenkins NA, Garber J, Kane M, Kolodner R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell. 1993;75:1027–1038. doi: 10.1016/0092-8674(93)90546-3. - DOI - PubMed
    1. Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A, et al. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature. 1994;368:258–261. doi: 10.1038/368258a0. - DOI - PubMed
    1. Whitehouse A, Meredith DM, Markham AF. DNA mismatch repair genes and their association with colorectal cancer (Review) Int J Mol Med. 1998;1:469–474. - PubMed