Nederlands tijdschrift voor geneeskunde · 1999
[Genetics of colorectal cancer. II. Hereditary background of sporadic and familial colorectal cancer].
Аннотация на английскомСтатьяОбзорНазвание и аннотация: Перевод в очереди
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Menko F H, Griffioen G, Wijnen J T, Tops C M, Fodde R, Vasen H F
Аннотация
About 15% of patients with colorectal cancer have a positive family history: 5% have hereditary colorectal cancer (hereditary non-polyposis colorectal carcinoma (HNPCC), familial adenomatous polyposis (FAP) or some other hereditary syndrome), while in 10% no clear hereditary pattern can be recognized ('familial colorectal cancer'). In sporadic and in familial intestinal cancer, a demonstrable hereditary predisposition may undoubtedly exist. HNPCC is often characterized by microsatellite instability, i.e. an increased number of short DNA sequences in the DNA indicating a disorder in DNA repair and a mutation in a DNA 'mismatch repair' (MMR) gene. Indicative of hereditary bowel cancer on the basis of such an MMR gene mutation are: (a) presence of bowel cancer in > or = 3 relatives, (b) early age at the time of the diagnosis of 'bowel cancer', (c) multiple primary bowel tumours, (d) uterine cancer in the family and (e) bowel and uterine cancer in a woman. Recent data demand a new subdivision of hereditary bowel cancer, based upon both the clinical picture and the results of DNA-tests. The genetic alterations in colonic adenomas and carcinomas are known to a large extent. In future these insights may be important in clinical practice, such as a more individual determination of the patient's prognosis and accordingly, of the treatment and follow-up.
Предметные рубрики MeSH
AdenomaAdolescentAdultAgedBase Pair MismatchCarcinomaChildChild, PreschoolColorectal NeoplasmsDNA Mutational AnalysisDNA RepairFemaleGenes, MCCGenetic Predisposition to DiseaseGerm-Line MutationHumansMaleMicrosatellite RepeatsMiddle AgedNeoplasms, Multiple PrimaryNetherlandsSyndromeUterine Neoplasms