Loss of heterozygosity on chromosome 9q22.3 in microdissected basal cell carcinomas around the Semipalatinsk Nuclear Testing Site, Kazakhstan |
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Authors: | Iwata Kenji Takamura Noboru Nakashima Masahiro Alipov Gabit Mine Mariko Matsumoto Naomichi Yoshiura Koichiro Prouglo Yuriy Sekine Ichiro Katayama Ichiro Yamashita Shunichi |
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Affiliation: | Atomic Bomb Disease Institute, Nagasaki University School of Medicine, Department of Dermatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan. |
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Abstract: | A high incidence of skin cancers has been noted around the Semipalatinsk Nuclear Testing Site (SNTS) in Kazakhstan. Recently, basal cell carcinoma (BCC) susceptibility genes, human homolog of the Drosophila pathed gene (PTCH), and the xeroderma pigmentosa group A-complementing gene (XPA), have been cloned and localized on chromosome 9q22.3. To clarify the effect of low-dose irradiation on the occurrence of BCC, we used microdissection and polymerase chain reaction to identify loss of heterozygosity (LOH) at 9q22.3 using BCC samples obtained from this region. Ten Japanese samples were analyzed as controls. LOH with at least 1 marker was identified in 5 of 14 cases from around SNTS, whereas only 1 case with 1 marker was identified among the 10 Nagasaki cases. The total number of LOH alleles from SNTS (8 of 45) was significantly higher than the number from Nagasaki (1 of 26) (P = 0.03). The higher incidence of LOH on 9q22.3 in BCC from around SNTS suggests involvement of chronic low-dose irradiation by fallout from the test site as a factor in the cancers. |
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Keywords: | basal cell carcinoma 9q22.3 loss of heterozygosity Semipalatinsk Nuclear Testing Site |
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