DETECTION AND SEQUENCING OF P53 GENE-MUTATIONS IN BRONCHIAL BIOPSY SAMPLES IN PATIENTS WITH LUNG-CANCER

被引:24
|
作者
MITSUDOMI, T
LAM, S
SHIRAKUSA, T
GAZDAR, AF
机构
[1] NCI, NAVY MED ONCOL BRANCH, BETHESDA, MD 20892 USA
[2] NATL NAVAL MED CTR, BETHESDA, MD 20814 USA
[3] UNIV OCCUPAT & ENVIRONM HLTH, SCH MED, DEPT SURG 2, KITAKYUSHU, FUKUOKA 807, JAPAN
[4] VANCOUVER GEN HOSP, VANCOUVER V5Z 1M9, BC, CANADA
[5] UNIV TEXAS, SW MED CTR, SIMMONS CANC CTR, DALLAS, TX 75230 USA
[6] UNIV TEXAS, SW MED CTR, DEPT PATHOL, DALLAS, TX 75230 USA
关键词
D O I
10.1378/chest.104.2.362
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
We demonstrated the feasibility of detection of p53 gene mutations in bronchial biopsy samples from patients with lung cancer. Following DNA extraction from two to three pieces of bronchial tissue obtained by fiberoptic bronchoscopy, p53 gene mutations were screened using polymerase chain reaction/single-strand conformation polymorphism technique. We examined four bronchial biopsy specimens from patients with squamous cell carcinoma of the lung and detected one point mutation at codon 130 (C to G, Leu to Val). This technique will be very useful for studies on early detection of lung cancers or for an analysis of a suspected premalignant lesion. Furthermore, this technique enables us to know the status of oncogene or tumor suppressor gene at the time of diagnosis, which may be very useful for a treatment of patients with cancer in the not too distant future.
引用
收藏
页码:362 / 365
页数:4
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