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Localization of tumor suppressor gene candidates by cytogenetic and short tandem repeat analyses in tumorigenic human bronchial epithelial cells.
Weaver, D A; Hei, T K; Hukku, B; Demuth, J P; Crawford, E L; McRaven, J A; Girgis, S; Willey, J C.
Afiliación
  • Weaver DA; Department of Medicine, Medical College of Ohio, 3120 Glendale Avenue, Rupert Health Center, Room 0012, Toledo, OH 43614, USA.
Carcinogenesis ; 21(2): 205-11, 2000 Feb.
Article en En | MEDLINE | ID: mdl-10657959
Radon exposure is associated with increased risk for bronchogenic carcinoma. Mutagenesis analyses have revealed that radon induces mostly multi-locus chromosome deletions. Based on these findings, it was hypothesized that deletion analysis of multiple radon-induced malignant transformants would reveal common mutations in chromosomal regions containing tumor suppressor genes responsible for malignant transformation. This hypothesis was supported by a previous study in which tumorigenic derivatives of the human papillomavirus 18-immortalized human bronchial epithelial cell line BEP2D were established following irradiation with 30 cGy of high linear energy transfer radon-simulated alpha-particles. Herein, we describe the analyses of 10 additional tumorigenic derivative cell lines resulting from the irradiation of five additional independent BEP2D populations. The new transformants have common cytogenetic changes, including the loss of chromosome (ch)Y, one of three copies of ch8, one of two copies of ch11p15-pter and one of three copies of ch14. These changes are the same as those reported previously. Analysis of PCR-amplified short tandem repeats of informative loci confirmed the loss of heterozygosity (LOH) at 12 loci spanning the length of ch8 in cell lines from four of the total of eight irradiation treatments to date and the loss of chY in all cell lines (8 of 8). LOH analysis with a total of 17 informative loci confirmed loss on ch14 in transformants from seven of eight irradiation treatments and indicated a 0.5-1.7 cM region of common involvement centered around locus D14S306. No LOH was detected at any of the informative loci on ch11. The overall results support our stated hypothesis. Further studies are currently in progress to determine whether the ch8 and ch14 regions contain genes with tumor suppressor function in bronchial epithelial cells.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 8 / Cromosomas Humanos Par 14 / Bronquios / Secuencias Repetitivas de Ácidos Nucleicos / Genes Supresores de Tumor / Cocarcinogénesis / Neoplasias Pulmonares / Neoplasias Inducidas por Radiación Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Carcinogenesis Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 8 / Cromosomas Humanos Par 14 / Bronquios / Secuencias Repetitivas de Ácidos Nucleicos / Genes Supresores de Tumor / Cocarcinogénesis / Neoplasias Pulmonares / Neoplasias Inducidas por Radiación Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Carcinogenesis Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido