## Background: In hong kong, lung carcinomas contribute to the majority of cancer deaths among chinese. point mutational activation of ras oncogenes has been observed in several populations. the incidence of these mutations in hong kong lung carcinomas was investigated. ## Methods: Lung resection
Detection and evaluation of p53 intron 2 polymorphism in lung carcinomas in Hong Kong
β Scribed by Hong Ge; Wah K. Lam; Joseph Lee; Maria P. Wong; Kin H. Fu; Wing W. Yew; Maria L. Lung
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- French
- Weight
- 618 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
A polymorphism in intron 2 of the p53 gene, which gives rise to 2 alleles, A l and A2, was analyzed by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and direct DNA-sequencing techniques. The distribution of this allele in the peripheral blood in the Chinese population comprising 27 healthy individuals, 30 bronchiectasis patients, 34 non-small-cell lung cancer (NSCLC) patients and 27 SCLC patients was analyzed. The genotypic distributions for this marker were significantly different between the blood of healthy individuals and SCLC patients. There was no significant difference between genotypes of Caucasians and Chinese. Tumors, normal lungs and peripheral blood of 83 adenocarcinoma and I0 squamous cell carcinoma patients were also studied. There was a significant difference in the distribution of the genotypes detected in tumor tissues vf. blood of adenocarcinoma patients. The frequency of detection of the A / / A / genotype in the tumor tissues was increased in adenocarcinoma patients as compared with the blood of adenocarcinoma patients and was decreased in the blood of SCLC patients as compared with the blood of healthy individuals. Survival rates in Hong Kong adenocarcinoma patients with the A / / A / genotype were lower than those in patients with A / /A2 and A2/A2 genotypes up to 30 months post-operation. Point mutations were detected at the p53 intron 2 polymorphic locus in NSCLC specimens, with a mutation rate of 15.4% (8/52). All mutations were GC transversions.
The significance of this instability in p53 intron 2 remains to be elucidated.
π SIMILAR VOLUMES
## Abstract The etiology of lung cancer in population with little or no tobacco exposure is not well understood. Individual genetic susceptibility factors have been suggested to contribute to lung cancer risk in this population. Mutations in the p53 tumor suppressor gene are implicated in the devel
Ninety-four patients with transitional cell carcinoma (TCC) of the renal pelvis and ureter, including dysplastic lesions, were studied for p53 and bcl-2 protein expression by immunohistochemistry. Twenty-one patients were also studied for p53 gene mutations by direct sequencing and for bcl-2 gene re
## Abstract ## BACKGROUND Investigation of the relation between primary tumor and metastatic disease is necessary for the identification of predictive factors for postrecurrence survival (PRS) in patients with recurrent osteosarcoma. ## METHODS Cellular levels of Pβglycoprotein, ErbBβ2, p53, and