International Journal of Cancer Management
The Official Journal of Cancer Research Center (CRC), Shahid Beheshti University of Medical Sciences
Mutations in the PTEN/MMAC1 Gene Associated with Cowden Disease and Juvenile Polyposis Syndrome
Abstract
Objective: In this study, we evaluated PTEN mutations in Cowden Disease and Juvenile Polyposis syndrome. PTEN mutations were detected, cancer and other phenotypes associated with each of these mutations were characterized and loss of wild type PTEN allele in the associated tumors was demonstrated.
Methods: Out of 9 patients included in this study, 8 had Juvenile polyposis and 1 had Cowden syndrome. PTEN gene was evaluated by means of polymerase chain reaction, single strand conformation polymorphism (SSCP), Heteroduplex mobility assay (HMA) and direct DNA sequencing.
Results: According to the results of this research, nucleotide substitutions in PTEN gene were found in 22٪ (9.2) of patients. The samples were found to be heterozygote for the c.341 T>G and c.389G>A mutations. One novel mutation c.341 T>G in Iranian patients with Cowden syndrome was found in this study.
Conclusions: The study of these rare patients could provide insight into PTEN driven tumorgenesis.
Copyright
© 2008, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Similar Articles
Heteroduplex Analysis of Causative APC Mutations in FAP Patients Referred for Genetic Counseling in Mashhad Ghaem Hospital, Iran
Hamzehloei T, A S. Heteroduplex Analysis of Causative APC Mutations in FAP Patients Referred for Genetic Counseling in Mashhad Ghaem Hospital, Iran. Shiraz E-Med J. 2013;14(4):e18537. doi: https://doi.org/10.17795/semj18537
Mutational Analysis of the PTEN/MMAC1 Tumor Suppressor Gene in Sporadic Glioblastoma Multiforme
Heshmatpour N, Tavassoli R, Mahzouni P. Mutational Analysis of the PTEN/MMAC1 Tumor Suppressor Gene in Sporadic Glioblastoma Multiforme. Int J Cancer Manag. 2011;4(2):e80730. doi:
Analysis of Hotspot PIK3CA Mutations (E542K and E545K) in Iranian Colorectal Cancer Patients
Behmanesh MA, Masouri Z, Abyaz MR, Habibimoghadam H, Moridnia A. Analysis of Hotspot PIK3CA Mutations (E542K and E545K) in Iranian Colorectal Cancer Patients. J Adv Immunopharmacol. 2024;4(4):e162972. doi: https://doi.org/10.5812/jai-162972
Clinical and Laboratory Characteristics of a Large Iranian Kindred Afflicted with Von Hippel Lindau Disease
Mir Saeid Ghazi AA, Amouzegar A, Zadeh-Vakili A, Sheikh Rezaei A, Amirbaigloo A, et al. Clinical and Laboratory Characteristics of a Large Iranian Kindred Afflicted with Von Hippel Lindau Disease. Int J Endocrinol Metab. 2021;19(2):e105189. doi: https://doi.org/10.5812/ijem.105189
A Novel Mutation of SLC26A4 Gene In an Iranian Family with Pendred Syndrome
Kahrizi K, Nishimura C, Naghavi A, Riazalhosseini Y, Smith R, et al. A Novel Mutation of SLC26A4 Gene In an Iranian Family with Pendred Syndrome. Int J Endocrinol Metab. 2005;3(2):. doi:
- Scopus by DOI: 0
Last Update: 3 weeks ago
- Scopus by Title: 0
Last Update: 3 weeks ago
- Scopus by Title (Ref): 1
Last Update: 3 weeks ago
- CrossRef: 0
Last Update: 15 hours ago
Ordering Reprints
Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC
Author(s):