4.5 Article

Somatic targeted mutation profiling of colorectal cancer precursor lesions

期刊

BMC MEDICAL GENOMICS
卷 15, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12920-022-01294-w

关键词

Screening; Adenoma; Serrated polyps; Mutation; Molecular profiling; Brazil

资金

  1. postgraduate program of Barretos Cancer Hospital
  2. Brazilian Federal Agency for the Support and Evaluation of Graduate Education (CAPES, Brazil)
  3. Barretos Cancer Hospital
  4. National Council for Scientific and Technological Development (CNPq, Brazil)

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This study characterized the mutation profile of colorectal cancer precursor lesions in a Brazilian population, revealing differences in the frequencies of mutations in genes such as APC, KRAS, TP53, and BRAF. These findings provide important insights into the biological history of colorectal cancer and support the potential use of these biomarkers in detecting precursor lesions during CRC screening in the Brazilian population.
Background Most colorectal cancers (CRC) arise from precursor lesions. This study aimed to characterize the mutation profile of colorectal cancer precursor lesions in a Brazilian population. Methods In total, 90 formalin-fixed paraffin-embedded colorectal precursor lesions, including 67 adenomas, 7 sessile serrated lesions, and 16 hyperplastic polyps, were analyzed by next-generation sequencing using a panel of 50 oncogenes and tumor suppressor genes. The genetic ancestry of the patients was estimated. Results Somatic driver mutations were identified in 66.7% of cases, including alterations in APC (32.2%), TP53 (20.0%), KRAS (18.9%), BRAF (13.3%) and EGFR (7.8%). Adenomas displayed a higher number of mutations, mainly in APC, compared to serrated polyps (73.1% vs. 47.8%, p = 0.026). Advanced adenomas had a significantly higher frequency of mutation in KRAS and a high overall mutation rate than early adenomas (92.9% vs. 59%, p = 0.006). A high degree of ancestry admixture was observed in the population studied, with a predominance of European components (mean of 73%) followed by African (mean of 11.3%). No association between genetic ancestry and type of lesions was found. The mutation profile of Brazilian colorectal precursor lesions exhibits alteration in APC, KRAS, TP53, and BRAF at different frequencies according to lesion type. Conclusions These results bestow the knowledge of CRC's biologic history and support the potential of these biomarkers for precursor lesions detection in CRC screening of the Brazilian population.

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