The multifaceted functions of homologous recombination in dealing with replication-associated DNA damages
DNA Repair, ISSN: 1568-7864, Vol: 129, Page: 103548
2023
- 9Citations
- 39Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations9
- Citation Indexes9
- CrossRef9
- Captures39
- Readers39
- 39
Article Description
The perturbation of DNA replication, a phenomena termed “replication stress”, is a driving force of genome instability and a hallmark of cancer cells. Among the DNA repair mechanisms that contribute to tolerating replication stress, the homologous recombination pathway is central to the alteration of replication fork progression. In many organisms, defects in the homologous recombination machinery result in increased cell sensitivity to replication-blocking agents and a higher risk of cancer in humans. Moreover, the status of homologous recombination in cancer cells often correlates with the efficacy of anti-cancer treatment. In this review, we discuss our current understanding of the different functions of homologous recombination in fixing replication-associated DNA damage and contributing to complete genome duplication. We also examine which functions are pivotal in preventing cancer and genome instability.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1568786423001027; http://dx.doi.org/10.1016/j.dnarep.2023.103548; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85166633579&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37541027; https://linkinghub.elsevier.com/retrieve/pii/S1568786423001027; https://dx.doi.org/10.1016/j.dnarep.2023.103548
Elsevier BV
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