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Mutational analysis of p53 and RB2/p130 genes in Malaysian nasopharyngeal carcinoma samples: a preliminary report

Hoe, Susan Ling Ling, and Sam, CK, (2006) Mutational analysis of p53 and RB2/p130 genes in Malaysian nasopharyngeal carcinoma samples: a preliminary report. Malaysian Journal of Pathology, 28 (1). pp. 35-39. ISSN 0126-8635

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Official URL: http://www.mjpath.org.my

Affiliations

Institute for Medical Research. Cancer Research Centre
University of Malaya. Institute of Biological Sciences

Abstract

This study reports the results of mutation detection of tumour suppressor genes, p53 and RB2/p130 genes in Malaysian nasopharyngeal carcinoma (NPC) studied by PCR-CSGE analysis and direct DNA sequencing method. Frequent sites of mutation in both genes (exons 5-8 of p53 and exons 19-21 of RB2/p130) were examined. Thirty-six NPC blood samples and three NPC cell lines were investigated for the presence of mutations. No mutation of p53 and RB2/p130 genes was identified in any of the blood samples. Nonetheless, there was an identical G → C nucleotide change at codon 280 of p53 gene in all the cell lines. A larger study that includes biopsy tissues should be carried out to provide a more in-depth look into the pathogenesis of NPC in Malaysia.

Item Type:Journal
Keywords:PCR-CSGE assay, mutation, nasopharyngeal carcinoma
Subjects:R Medicine
ID Code:1778

Lo KW, To KF, Huang DP. Focus on nasopharyngeal carcinoma. Cancer Cell 2004; 5: 423-8.

GCC Lim, Y Halimah (Eds). Second report of the National Cancer Registry. Cancer incidence in Malaysia 2003. National Cancer Registry. Kuala Lumpur 2004.

Spano JP, Busson P, Atlan D, Bourhis J, Pignon JP, Esteban C, Armand JP. Nasopharyngeal carcinomas: An update. Eur J Cancer 2003; 39: 2121-35.

Chakrani F, Armand JP, Lenoir G, Ju LY, Liang JP, May E, May P. Mutations clustered in exon 5 of the p53 gene in primary nasopharyngeal carcinomas from South-Eastern Asia. Int J Cancer 1995; 61: 316-20.

Sun Y, Hegamyer G, Cheng YJ, Hildesheim A, Chen JY, Chen IH, Cao Y, Yao KT, Colburn NH. An infrequent point mutation of p53 gene in human nasopharyngeal carcinoma. Proc Natl Acad Sci USA 1992; 89: 6516-20.

Niedobitek G, Agathanggelou A, Barber P, Smallman LA, Jones EL, Young LS. p53 expression and EBV infection in undifferentiated and squamous cell 457-61.

Agaoglu FY, Dizdar Y, Dogan O, Alatli C, Ayau I, Savci N, Tas S, Dalay N, Altun M. p53 overexpression in nasopharyngeal carcinoma. In Vivo 2004; 18: 555-60.

Lo KW, Mok CH, Huang DP, Liu YX, Choi PH, Lee JC, Tsao SW. p53 mutation in human nasopharyngeal carcinoma. Anticancer Res 1992; 12: 1957-63.

Burgos JS. Absence of p53 alterations in NPC Spanish patients with Epstein-Barr infection. Virus Genes 2003; 27: 263-68.

Sun Y, Hegamyer G, Colburn NH. Nasopharyngeal carcinoma shows no detectable retinoblastoma susceptibility gene alterations. Oncogene 1993; 8: 791-5.

Claudio PP, Howard CM, Fu Y, Cinti C, Califano L, Micheli P, Mercer EW, Caputi M, Giordano A. Mutations in the RB-related gene RB2/p130 in primary nasopharyngeal carcinoma. Cancer Res 2000; 60: 8-12.

Chang KP, Hao SP, Lin SY, Tsao KC, Kuo TT, Tsai MH, Tseng CK, Tsang NM. A lack of association between p53 mutations and recurrent nasopharyngeal carcinomas refractory to radiotherapy. Laryngoscope 2002; 112: 2015-9.

Ganguly A, Rock MJ, Prockop DJ. Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments. Proc Natl Acad Sci USA 1993; 90: 10325-9.

Levine AJ, Momand J, Finlay CA. The p53 tumor suppressor gene. Nature 1991; 351: 453-6.

Paggi MG, Giordano A. Who is the boss in the retinoblastoma family? The point of view of RB2/p130, the little brother. Cancer Res 2001; 61: 4651-4.

Alvi AJ, Hogg R, Rader JS, Kuo MJ, Maher ER, Latif F. Mutation screening analysis of the retinoblastoma-related gene RB2/p130 in sporadic ovarian cancer and head and neck squamous cell cancer. Mol Pathol 2002; 55: 153-5.

Chang YS, Lin YJ, Tsai CN, Shu CH, Tsai MS, Choo KB, Lin ST. Detection of mutations in the p53 gene in human head and neck carcinomas by single strand conformation polymorphism analysis. Cancer Lett 1992; 67: 167-74.

Van Tornout JM, Spruck CH 3rd, Shibata A, Schmutte C, Gonzalez-Zulueta M, Nichols PW, Chandrasoma PT, Yu MC, Jones PA. Presence of p53 mutations in primary nasopharyngeal carcinoma (NPC) in non-Asians of Los Angeles, California, a low-risk population for NPC. Cancer Epidemiol Biomarkers Prev 1997; 6: 493-7.

Effert P, McCoy R, Abdel-Hamid M, Flynn K, Zhang Q, Busson P, Tursz T, Lin E, Raab-Traub N. Alterations of the p53 gene in nasopharyngeal carcinoma. J Virol 1992; 66: 3768-75.

Helin K, Holm K, Niebuhr A, Eiberg H, Tommerup N, Hougaard S, Poulsen HS, Spang-Thomsen M, Norgaard P. Loss of the retinoblastoma protein-related p130 protein in small cell lung carcinoma. Proc Natl Acad Sci USA 1997; 94: 6933-8.

Cinti C, Leoncini L, Nyongo A, Ferrari F, Lazzi S, Bellan C, Vatti R, Zamparelli A, Cevenini G, Tosi GM, Claudio PP, Maraldi NM, Tosi P, Giordano A. Genetic alterations of the retinoblastoma-related gene RB2/p130 identify different pathogenetic mechanisms in and among Burkitt’s lymphoma subtypes. Am J Pathol 2000; 156: 751-60.

Körkkö J, Annunen S, Pihlajamaa T, Prockop DJ, Ala-Kokko L. Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: Comparison with denaturing gradient gel electrophoresis and nucleotide sequencing. Proc Natl Acad Sci USA 1998; 95: 1681-5.

Ganguly A, Prockop DJ. Detection of mismatched bases in double-stranded DNA by gel electrophoresis. Electrophoresis 1995; 16: 1830-5.

Markoff A, Sormbroen H, Bogdanova N, Preisler-Adams S, Ganev V, Dworniczak B, Horst J. Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols. Eur J Hum Genet 1998; 6: 145-50.

Boardman LA, Schmidt S, Lindor NM, Burgart LJ, Cunningham JM, Price-Troska T, Snow K, Ahlquist DA, Thibodeau SN. A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair. Genes, Chromosomes & Cancer 2001; 30: 181-6.

Rapakko K, Kokkonen H, Leisti J. UBE3A gene mutations in Finnish Angelman syndrome patients detected by conformation sensitive gel electrophoresis. Am J Med Genet 2004; 126A: 248-52.

Uyeda T. Takahashi T, Eto S, Sato T, Xu G, Kanezaki R, Toki T, Yonesaka S, Ito E. Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients. J Hum Genet 2004; 49: 404-7.

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