Correlation between tumor stage and presence or absence of germline RB1 mutation.

<p>Correlation between tumor stage and presence or absence of germline RB1 mutation.</p

Frequency of somatic RB1 mutations in RB Tunisian patients (not including LOH).

<p>Frequency of somatic RB1 mutations in RB Tunisian patients (not including LOH).</p

Mutation Spectrum of <i>RB1</i> Gene in Unilateral Retinoblastoma Cases from Tunisia and Correlations with Clinical Features

<div><p>Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common primary intraocular malignancy in children. Somatic inactivation of both alleles of the <i>RB1</i> tumor suppressor gene in a retinal progenitor cell through diverse mechanisms including genetic and epigenetic modifications, is the crucial event in initiation of tumorigenesis in most cases of isolated unilateral retinoblastoma. We analyzed DNA from tumor tissue and from peripheral blood to determine the <i>RB1</i> mutation status and seek correlations with clinical features of 37 unrelated cases of Tunisian origin with sporadic retinoblastoma. All cases were unilateral except one who presented with bilateral disease, in whom no germline coding sequence alteration was identified. A multi-step mutation scanning protocol identified bi-allelic inactivation of <i>RB1</i> gene in 30 (81%) of the samples tested. A total of 7 novel mutations were identified. There were three tumors without any detectable mutation while a subset contained multiple mutations in <i>RB1</i> gene. The latter group included tumors collected after treatment with chemotherapy. There were seven individuals with germline mutations and all presented with advanced stage of tumor. There was no difference in age of onset of RB based on the germline mutation status. Thus 20% of the individuals with sporadic unilateral RB in this series carried germline mutations and indicate the importance of genetic testing all children with sporadic retinoblastoma. These findings help to characterize the spectrum of mutations present in the Tunisian population and can improve genetic diagnosis of retinoblastoma.</p></div

Somatic variations of unknown signficance identified within <i>RB1</i> gene.

<p>Nucleotide numbering for genomic DNA and cDNA are according to GenBank accession numbers L11910.1 and NM_000321.2, respectively. Amino acid numbering refers to the reference sequence for pRB protein, NP_000312.2.</p><p>Somatic variations of unknown signficance identified within <i>RB1</i> gene.</p