印度骨肉瘤患者p53低水平突变及其与骨中氟化物水平的相关性

N. Ramesh, A. S. Vuayaraghavan, B. Desai, M. Natarajan, P. B. Murthy, K. S. Pillai
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引用次数: 9

摘要

骨肉瘤的发病机制尚不清楚。最近,慢性氟化物暴露已被认为有可能的病因作用,引起非特异性成骨细胞增殖。我们有兴趣探索氟化物骨含量和p53突变之间的可能关系。我们分析了骨肉瘤组织中各种外显子的p53突变,并将这些发现与印度患者的骨氟化物水平联系起来。我们分析了来自20名骨肉瘤患者的组织样本,以寻找可能的基因改变,包括突变,并评估了骨骼中氟化物积聚的程度。显示电泳迁移率改变的片段被证实具有突变序列。2例(10%)样本中观察到突变。18个样本显示骨骼氟化物含量在1000到27,000 ppm之间,而2个突变样本的氟化物含量分别为64,000和89,000 ppm。高水平的骨氟化物水平和氟化物诱导的DNA损伤与化学诱导的p53突变之间的作用机制的相似性使我们提出高氟化物骨含量可能是导致骨肉瘤的主要因素之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low levels of p53 mutations in Indian patients with osteosarcoma and the correlation with fluoride levels in bone.
The pathogenesis of osteogenic sarcoma is not known. Recently, chronic fluoride exposure has been incriminated as having a possible etiologic role by causing a nonspecific osteoblast proliferation. We were interested in exploring the possible relationship between fluoride bone content and p53 mutations. We analyzed p53 mutations in various exons in tissue of osteosarcoma, and correlated the findings with the bone fluoride levels in Indian patients. We analyzed tissue samples from 20 osteosarcoma patients for possible genetic alterations including mutations, and we assessed the extent of fluoride accumulation in bone. Fragments displaying an altered electrophoretic mobility were confirmed as having mutated sequences. Mutation was observed in samples of two cases (10% incidence). Eighteen samples showed bone fluoride levels between 1000 and 27,000 ppm, whereas the 2 mutated samples showed fluoride levels of 64,000 and 89,000 ppm, respectively. The high levels of bone fluoride levels and the similarity of the mechanisms of action between fluoride-induced DNA damage and chemically-induced p53 mutations lead us to propose that high fluoride bone content might have been one of the major factors causing osteosarcoma.
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