Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer

Breast cancer is one of the most prevalent malignancies and the most common cancer in female patients. In recent years, the clinical utilization of a class of drugs called poly (ADP-ribose) polymerase inhibitors has been observed to be detrimental to cells that harbor defective DNA damage repair mec...

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Main Authors: Mehdi Sadeghi, Mohammad Reza Karimi, Amir Hossein Karimi
Format: Article
Language:English
Published: University of Mazandaran 2024-02-01
Series:Journal of Genetic Resources
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Online Access:https://sc.journals.umz.ac.ir/article_4890_8548169c4f0f6f16315afab81c65c22f.pdf
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author Mehdi Sadeghi
Mohammad Reza Karimi
Amir Hossein Karimi
author_facet Mehdi Sadeghi
Mohammad Reza Karimi
Amir Hossein Karimi
author_sort Mehdi Sadeghi
collection DOAJ
description Breast cancer is one of the most prevalent malignancies and the most common cancer in female patients. In recent years, the clinical utilization of a class of drugs called poly (ADP-ribose) polymerase inhibitors has been observed to be detrimental to cells that harbor defective DNA damage repair mechanisms. Implementation of these drugs entails a series of unprecedented challenges, including the development of drug resistance to this treatment strategy. Thus, it is essential to gain a better understanding of the mechanisms that regulate the DNA damage response to maximize the treatment efficacy in breast cancer patients and minimize unwanted side effects. In this study, through the utilization of single-cell- and bulk-level transcriptional data, we set out to identify molecules and molecular circuits associated with DNA damage response in breast cancer patients. By identifying differentially expressed genes in single-cell cancer cell populations inherently different in DNA damage response, further clustering bulk RNA-sequencing samples based on the expression of these genes, and performing network and enrichment analysis at the bulk level, we have characterized breast cancer samples based on their DNA damage response. Moreover, we have been able to identify a central network module whose members can serve as treatment targets and yield further insights into the mechanisms of drug resistance and DNA damage response in breast cancer. Overall, this study contributes to the characterization of the transcriptional circuits involved in the heterogeneity of DDR in breast cancer and provides candidate avenues for the investigation of potential therapeutic interventions.
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spelling doaj-art-a7df9d88ff6f49b688991b16a3de32162025-01-27T06:11:19ZengUniversity of MazandaranJournal of Genetic Resources2423-42572588-25892024-02-01101576510.22080/jgr.2024.26741.13844890Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast CancerMehdi Sadeghi0Mohammad Reza Karimi1Amir Hossein Karimi2Department of Cell and Molecular Biology, Faculty of Science, Semnan University, Semnan, IranMichael G. DeGroote School of Medicine, Department of Biochemistry and Biomedical Science, McMaster University, Hamilton, CanadaDepartment of Pathology and Laboratory Medicine, University of Western Ontario, London, Ontario, CanadaBreast cancer is one of the most prevalent malignancies and the most common cancer in female patients. In recent years, the clinical utilization of a class of drugs called poly (ADP-ribose) polymerase inhibitors has been observed to be detrimental to cells that harbor defective DNA damage repair mechanisms. Implementation of these drugs entails a series of unprecedented challenges, including the development of drug resistance to this treatment strategy. Thus, it is essential to gain a better understanding of the mechanisms that regulate the DNA damage response to maximize the treatment efficacy in breast cancer patients and minimize unwanted side effects. In this study, through the utilization of single-cell- and bulk-level transcriptional data, we set out to identify molecules and molecular circuits associated with DNA damage response in breast cancer patients. By identifying differentially expressed genes in single-cell cancer cell populations inherently different in DNA damage response, further clustering bulk RNA-sequencing samples based on the expression of these genes, and performing network and enrichment analysis at the bulk level, we have characterized breast cancer samples based on their DNA damage response. Moreover, we have been able to identify a central network module whose members can serve as treatment targets and yield further insights into the mechanisms of drug resistance and DNA damage response in breast cancer. Overall, this study contributes to the characterization of the transcriptional circuits involved in the heterogeneity of DDR in breast cancer and provides candidate avenues for the investigation of potential therapeutic interventions.https://sc.journals.umz.ac.ir/article_4890_8548169c4f0f6f16315afab81c65c22f.pdfbreast cancerdna damage responsesingle-cell sequencinggenomicstranscriptomics
spellingShingle Mehdi Sadeghi
Mohammad Reza Karimi
Amir Hossein Karimi
Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer
Journal of Genetic Resources
breast cancer
dna damage response
single-cell sequencing
genomics
transcriptomics
title Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer
title_full Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer
title_fullStr Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer
title_full_unstemmed Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer
title_short Identification of the Genomics and Transcriptomics Regulators of the DNA Damage Response in Breast Cancer
title_sort identification of the genomics and transcriptomics regulators of the dna damage response in breast cancer
topic breast cancer
dna damage response
single-cell sequencing
genomics
transcriptomics
url https://sc.journals.umz.ac.ir/article_4890_8548169c4f0f6f16315afab81c65c22f.pdf
work_keys_str_mv AT mehdisadeghi identificationofthegenomicsandtranscriptomicsregulatorsofthednadamageresponseinbreastcancer
AT mohammadrezakarimi identificationofthegenomicsandtranscriptomicsregulatorsofthednadamageresponseinbreastcancer
AT amirhosseinkarimi identificationofthegenomicsandtranscriptomicsregulatorsofthednadamageresponseinbreastcancer