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Detection of microsatellite instability in sporadic cardiac myxomas

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Autore
Sourvinos, G.; Parissis, J.; Sotsiou, F.; Arvanitis, D. L.; Spandidos, D. A.
Data
1999
DOI
10.1016/s0008-6363(98)00339-3
Soggetto
cardiac myxomas
heart tumours
microsatellite instability
molecular
biology
polymerase chain reaction
experimental
heart
GENETIC INSTABILITY
COLORECTAL-CANCER
CARCINOMA
SEQUENCES
HETEROZYGOSITY
MECHANISM
REPEAT
TUMORS
Cardiac & Cardiovascular Systems
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Abstract
Objective: Microsatellite instability (MIN) is an early event in DNA repair-deficient associated diseases and reflects an elevated mutation rate in the genome of neoplastic cells. Sporadic cardiac myxomas are the most common primary heart tumours and their aetiopathology remains obscure. This study investigates the incidence of MIN in sporadic cardiac myxomas as a possible genetic mechanism of tumour pathogenesis. Methods: Eleven surgically excised sporadic cardiac myxomas were assessed for MI using twenty-two highly polymorphic microsatellite markers, located on a wide range of chromosomal arms. DNA was extracted from myxoma tissue specimens as well as the respective normal tissue and subjected to polymerase chain reaction. Results: The microsatellite analysis revealed that seven myxoma specimens (64%) exhibited MIN in at least one marker. One tumour specimen exhibited evidence of MIN in four microsatellite markers, while the most frequently affected marker was D17S855 (27%), located on chromosome 17q. Discussion: We have detected a considerable incidence of MIN in sporadic cardiac myxomas indicating that decreased fidelity in DNA replication and repair is common in these tumours. To the best of our knowledge this is the first report describing MIN in sporadic cardiac myxomas, as a possible pathogenetic mechanism of these rare neoplasms. (C) 1999 Elsevier Science B.V. All rights reserved.
URI
http://hdl.handle.net/11615/33227
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