Literature DB >> 33584808

ANKLE1 as New Hotspot Mutation for Breast Cancer in Indian Population and Has a Role in DNA Damage and Repair in Mammalian Cells.

Divya Bakshi1, Archana Katoch2,3, Souneek Chakraborty2,3, Ruchi Shah1, Bhanu Sharma1, Amrita Bhat1, Sonali Verma1, Gh Rasool Bhat1, Ashna Nagpal1, Samantha Vaishnavi4, Anindya Goswami2,3, Rakesh Kumar1.   

Abstract

Breast cancer has replaced cervical cancer as being the most common and having the highest mortality among women in India. ANKLE gene is conserved among organisms during evolutionary succession and is a member of LEM family proteins in lower metazoans and is involved in critical functions in the nuclear architecture, gene expression and cell signaling. ANKLE1 is the human orthologous of LEM-3 and is involved in DNA damage response and DNA repair. Whole Exome Sequencing (WES) of paired breast cancer samples was performed and ANKLE1 was found to be a new possible hotspot for predisposition of breast cancer. The mass array genotyping for breast cancer variant rs2363956 further confirmed the ANKLE1 association with the studied population of breast cancer. To elucidate the role of ANKLE1 in DNA damage, it was knocked down in MCF-7 breast cancer cell line and the expression of γH2AX was assessed. ANKLE1 knockdown cells displayed elevated levels of γ-H2AX foci in response to the cisplatin induced replication stress. The localization pattern of ANKLE1 further emphasized the role of ANKLE1 in DNA repair process. We observed that ANKLE1 is required for maintaining genomic stability and plays a role in DNA damage and repair process. These findings provided a molecular basis for the suspected role of ANKLE1 in human breast cancer and suggested an important role of this gene in controlling breast cancer development among women in India.
Copyright © 2021 Bakshi, Katoch, Chakraborty, Shah, Sharma, Bhat, Verma, Bhat, Nagpal, Vaishnavi, Goswami and Kumar.

Entities:  

Keywords:  ANKLE-1; DNA damage; MCF-7 cell line; breast cancer; cancer; γH2AX

Year:  2021        PMID: 33584808      PMCID: PMC7873468          DOI: 10.3389/fgene.2020.609758

Source DB:  PubMed          Journal:  Front Genet        ISSN: 1664-8021            Impact factor:   4.599


  34 in total

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