- Meeting abstract
- Open Access
Diagnostic microarray test for a genetic predisposition to hereditary nonpolyposis colorectal cancer (HNPCC)
Hereditary Cancer in Clinical Practice volume 10, Article number: A23 (2012)
Colorectal cancer (CC), due to its frequency and social costs is a subject of extensive screening programs (colonoscopy and new developments) in several countries, including Poland. Relatively common and defined genetic predispositions to different forms of CC make genetic screening an attractive alternative, not only in families with positive CC history. Optimal testing strategy should be acceptable for subjects, high-throughput and cost-effective in mutation detection.
CBDNA Ltd. Company has developed and validated prototype diagnostic microarray test for genetic predisposition to nonpolyposis colorectal cancer (HNPCC). The test includes 169 selected mutations (point mutations and short insertions/deletions) in 5 genes: MLH1, MSH2, MSH6, CHEK2 and NOD2. Total of 36 patients with CC, six of them fulfilling modified Amsterdam criteria for HNPCC, and the rest with less evident familial aggregation of cancers were included in the pilot study. Altogether 6 different mutations in 9 patients were identified (25%) within the group.
The effectiveness of genetic screening using the microarray method was similar to other molecular, but more expensive and time-consuming methods.
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Kaszuba, M., Sikorski, A., Odważna, J. et al. Diagnostic microarray test for a genetic predisposition to hereditary nonpolyposis colorectal cancer (HNPCC). Hered Cancer Clin Pract 10, A23 (2012). https://doi.org/10.1186/1897-4287-10-S4-A23
- Colorectal Cancer
- Pilot Study
- Point Mutation
- Screening Program
- Genetic Predisposition