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Alterations of ATM and CADM1 in chromosomal 11q22.3–23.2 region are associated with the development of invasive cervical carcinoma

机译:染色体11q22.3-23.2区ATM和CADM1的改变与浸润性宫颈癌的发展有关

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摘要

To understand the importance of chr11q22.3–23.2 region in the development of cervical cancer, we have studied the genetic and epigenetic alterations of the candidate genes ATM, PPP2R1B, SDHD and CADM1 in cervical intraepithelial neoplasia (CIN) and cervical carcinoma (CACX) samples. Our study revealed low expression and high alterations (methylation/deletion) (55–59%) of ATM and CADM1 genes along with poor patient outcome. The alterations of ATM and CADM1 are associated with the progression of tumor from CIN to Stage I/II, thus implying their role in early invasiveness. The two genes, PPP2R1B and SDHD, lying in between ATM and CADM1, have low frequency of alterations, and majority of the alterations are in CACX samples, indicating that their alterations might be associated with disease progression. Expressions (mRNA/protein) of the genes showed concordance with their molecular alterations. Significant co-alteration of ATM and CADM1 points to their synergic action for the development of CACX. Mutation is, however, a rare phenomenon for inactivation of ATM. Association between the alteration of ATM and CHEK1 and poor survival of the patients having co-alterations of ATM and CHEK1 points to the DNA damage response pathway disruption in development of CACX. Thus, our data suggest that inactivation of ATM–CHEK1-associated DNA damage response pathway and CADM1-associated signaling network might have an important role in the development of CACX.
机译:为了了解chr11q22.3–23.2区域在宫颈癌发展中的重要性,我们研究了宫颈上皮内瘤变(CIN)和宫颈癌(CACX)候选基因ATM,PPP2R1B,SDHD和CADM1的遗传和表观遗传学改变样品。我们的研究揭示了ATM和CADM1基因的低表达和高改变(甲基化/缺失)(55-59%)以及患者预后不良。 ATM和CADM1的改变与肿瘤从CIN到I / II期的进展有关,因此暗示它们在早期侵袭性中的作用。位于ATM和CADM1之间的两个基因PPP2R1B和SDHD发生变化的频率较低,并且大多数变化发生在CACX样本中,表明它们的变化可能与疾病进展有关。基因的表达(mRNA /蛋白质)与它们的分子变化一致。 ATM和CADM1的显着共同意义在于它们对CACX开发的协同作用。但是,突变是ATM失活的罕见现象。 ATM和CHEK1的改变与具有ATM和CHEK1共同改变的患者的不良生存之间的关联表明,CACX发育中的DNA损伤反应途径被破坏。因此,我们的数据表明,ATM–CHEK1相关的DNA损伤反应途径和CADM1相关的信号网络的失活可能在CACX的发展中起重要作用。

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