Alterations of transforming growth factor beta receptor II, insulin growth factor receptor II genes in microsatellite unstable prostate carcinomas.

Abstract

DNA from 45 primary prostate tumors and corresponding normal tissues were analyzed to detect whether the alterations of transforming growth factor beta receptor II (TGFbetaRII) and insulin growth factor receptor II (IGFRII) are associated with microsatellite instability (MSI). We identified that 25 tumors were microsatellite unstable (55%). The remaining 20 tumors are found to be microsatellite stable. Loss of heterozygosity (LOH) was also tested at various loci. Results indicate that in case of TGFbetaRII, the rate of frame-shift mutation depends on the number of polyadenine [poly(A)] tracts. Twelve percent of the tumors had frame-shift alteration at BAT-RII locus which has 10 poly(A) repeats. Twenty percent of the tumors had frame-shift at BAT-25 locus which has 25 poly(A) repeats. In addition, IGFRII gene was examined for the presence of mutation in the repetitive sequences. Seven of the 25 tumors showed deletion of a G within eight poly(G) repeats. Besides these changes there were two tumors which showed a novel insertion of A within this poly(G) repeat making a change in 9 samples (R4, 36%). On the other hand, 4 tumors showed changes within the 5CT repeats. In addition, 3 tumors showed another novel insertion of C within the CT repeats.

• Authors: Nandan Bhattacharyya, Jianming Tao, Eric A Klein, Sipra Banerjee
• Journal: Oncology reports (Oncol Rep) Vol. 11 Issue 1 Pg. 231-6 (Jan 2004) ISSN: 1021-335X [Print] Greece
• PMID: 14654931 (Publication Type: Journal Article)

Chemical References

• DNA, Neoplasm
• Receptor, IGF Type 2
• Receptors, Transforming Growth Factor beta
• Protein Serine-Threonine Kinases
• Receptor, Transforming Growth Factor-beta Type II

Topics

• Base Sequence
• DNA Mutational Analysis
• DNA, Neoplasm (chemistry, genetics)
• Humans
• Loss of Heterozygosity
• Male
• Microsatellite Repeats (genetics)
• Mutagenesis, Insertional
• Polymerase Chain Reaction
• Prostatic Neoplasms (genetics, pathology)
• Protein Serine-Threonine Kinases
• Receptor, IGF Type 2 (genetics)
• Receptor, Transforming Growth Factor-beta Type II
• Receptors, Transforming Growth Factor beta (genetics)
• Sequence Deletion