Human genetics · 2011
Alterations of ATM and CADM1 in chromosomal 11q22.3-23.2 region are associated with the development of invasive cervical carcinoma.
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Mazumder Indra Dipanjana, Mitra Sraboni, Roy Anup, Mondal Ranajit Kumar, Basu Partha Sarathi, Roychoudhury Susanta, Chakravarty Runu, Panda Chinmay Kumar
Аннотация
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.
Предметные рубрики MeSH
Ataxia Telangiectasia Mutated ProteinsCell Adhesion Molecule-1Cell Adhesion MoleculesCell Cycle ProteinsCell Line, TumorCheckpoint Kinase 1Chromosome AberrationsChromosomes, Human, Pair 11DNA DamageDNA MethylationDNA-Binding ProteinsDisease ProgressionEpigenomicsFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansImmunoglobulinsMutationNeoplasm StagingPapillomavirus InfectionsPromoter Regions, GeneticProtein KinasesProtein Phosphatase 2Protein Serine-Threonine KinasesSignal TransductionTumor Suppressor ProteinsUterine Cervical NeoplasmsUterine Cervical Dysplasia