Molecular genetic profiling of Filipino patients with retinoblastoma: A preliminary study
- Author:
Pia Magdalena R. Mendoza
1
;
Prospero Ma. C. Tuano
1
;
Lee G. Verzosa
1
;
Remedios Felisa S. Huerto
1
;
Ma. Luisa D. Enriquez
2
;
Emilio L. Macias
1
,
3
Author Information
- Publication Type:Journal Article
- Keywords: Gene mutation; Retinoblastoma susceptibility gene
- MeSH: Retinoblastoma; Genes, Retinoblastoma
- From: Philippine Journal of Ophthalmology 2012;37(1):39-44
- CountryPhilippines
- Language:English
-
Abstract:
Objective:To detect and characterize retinoblastoma susceptibility gene (RB1) mutations in tumor samples
collected from Filipino patients with retinoblastoma.
Methods:Six tumor samples were obtained from Filipino patients diagnosed with retinoblastoma. DNA was extracted from the tumor samples and exons 13-21 of the RB1 gene were amplified by polymerase chain reaction (PCR). PCR amplification products were subsequently purified and sequenced. Mutation detection and characterization were done by alignment of obtained sequences to the RB1 reference sequence from NCBI GenBank using Bioedit® software. The identified mutations were correlated with clinical presentation and family history. These mutations were also compared to known mutations reported in the RB1 Gene Mutation Leiden Open Variation Database (LOVD).
Results:Mutations were detected in two out of the six samples. In a patient with unilateral disease and no family history, two mutations were identified: a novel CGT>AGT (Arginine → Serine) missense mutation in position c.1861 of exon 19 and a previously reported CGA>TGA (Arginine → STOP) nonsense mutation in position c. 1735 of exon 18. A possible large exonic deletion was identified in a case of unilateral disease with no family history.
Conclusion:We were able to identify both novel and known mutations in the RB1 gene of Filipino retinoblastoma cases using DNA sequencing techniques. These techniques may be applied to further characterize the genetic mutations of Filipino retinoblastoma cases and their families in developing a rational method of genetic testing for early diagnosis and counseling. - Full text:PJO 76.pdf
