Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD)

Publication date

2018-10-01

Authors

Leenders, Erika K S M
Westdorp, Harm
Brüggemann, Roger J
Loeffen, Jan L.C.ISNI 0000000140730874
Kratz, Christian
Burn, John
Hoogerbrugge, Nicoline
Jongmans, Marjolijn C JISNI 0000000388139965

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Advisors

Supervisors

Document Type

Article

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License

taverne

Abstract

Constitutional MisMatch Repair Deficiency (CMMRD) is caused by homozygous or compound heterozygous germline variants in one of the mismatch repair (MMR) genes (MSH2, MSH6, PMS2, MLH1). This syndrome results in early onset colorectal cancer, leukemia and lymphoma, brain tumors and other malignancies. Children with CMMRD are at high risk of developing multiple cancers and cancer surveillance does not guarantee detection of cancer at a curable stage. The development of a preventive treatment strategy would be a major step forward. Long-term daily use of acetylsalicylic acid (ASA) has been shown to reduce cancer risk in individuals with Lynch syndrome (LS). LS is caused by heterozygous germline variants of MSH2, MSH6, PMS2 and MLH1 and characterized by an increased risk of developing colorectal and endometrial cancer at adult age. Here we discuss the potential use of ASA for cancer prevention in patients with CMMRD.

Keywords

Journal Article, Review, Colorectal Neoplasms/complications, Humans, Aspirin/therapeutic use, Neoplastic Syndromes, Hereditary/complications, Brain Neoplasms/complications, Mismatch Repair Endonuclease PMS2/genetics, Colorectal Neoplasms, Hereditary Nonpolyposis/complications, DNA-Binding Proteins/genetics, MutS Homolog 2 Protein/genetics, Germ-Line Mutation/genetics, Neoplasms/complications, MutL Protein Homolog 1/genetics, Child, Taverne, Genetics(clinical), Genetics, Review, Journal Article

Citation

Leenders, E K S M, Westdorp, H, Brüggemann, R J, Loeffen, J, Kratz, C, Burn, J, Hoogerbrugge, N & Jongmans, M C J 2018, 'Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD)', European Journal of Human Genetics, vol. 26, no. 10, pp. 1417-1423. https://doi.org/10.1038/s41431-018-0197-0