Eight-Hit Evolutionary Pattern in ATM Gene of a Breast Carcinoma Patient: A Personalized Approach

P. Mehdipour, Asaad Azarnezha
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引用次数: 1

Abstract

: Background : Different genetic variants in the ATM gene have been reported to be associated with breast carcinoma (BC). Purpose of the study was to consider the multi-insights experiments and explorations through the molecular, cellular and structural aspects of ATM. Methods and Results : D1853N polymorphism was traced in a proband with BC. DNA extracted from blood and tumor tissue was PCR-amplified and cloned to allelic localization of characterized variants. Protein expression and In silico analysis based on three different profiles involved in cell cycle were also performed to confirm mutational events. Findings revealed the molecular based sequential events as an eight-hit evolutionary pattern (8- Hit E.P) including D1853N as the first predisposing hit (inherited), pre-differentiation stage hits including IVS 36-8 T>C as the 2 nd hit, V1833M as the 3 rd hit, L1888L as the 4 th , and somatic variants including IVS 36-46 C>T, L1842L, H1864H, and S1872R were considered as the 5-8 th hits. Low protein expression of ATM in the majority of cells was observed, but the expression of cyclin E, CDC25A, P53, and Ki-67 was more diverse. Conclusions : Observations were reflective of the sequential molecular and cellular events through the entire patient’s life from the pre-differentiation embryonic stage and all through the post-birth periods. Mentioned hits seem to be effective on expression and function of ATM which confirmed by the expression and in silico analysis.
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乳腺癌患者ATM基因的八击进化模式:一种个性化的方法
背景:ATM基因的不同遗传变异已被报道与乳腺癌(BC)相关。本研究的目的是考虑从分子、细胞和结构方面对ATM的多视角实验和探索。方法与结果:1例BC先证者检测到D1853N多态性。从血液和肿瘤组织中提取的DNA进行pcr扩增并克隆到特征变异的等位基因定位。蛋白质表达和基于三种不同谱参与细胞周期的硅分析也进行了确认突变事件。结果表明,分子序列事件为8 Hit进化模式(8- Hit E.P),其中D1853N为第一个易感点(遗传),分化前阶段的IVS 36- 8t b> C为第2个易感点,V1833M为第3个易感点,L1888L为第4个易感点,体细胞变异包括IVS 36- 46c b> T、L1842L、H1864H和S1872R为第5-8个易感点。ATM蛋白在大多数细胞中低表达,但cyclin E、CDC25A、P53和Ki-67的表达更为多样化。结论:观察结果反映了患者从分化前胚胎期到出生后整个生命过程中连续发生的分子和细胞事件。通过表达和芯片分析证实,上述撞击似乎对ATM的表达和功能都有影响。
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