Chromatin Remodeling and DNA Repair Pathways in Cancer

A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Human Genomics and Genetic Diseases".

Deadline for manuscript submissions: 25 October 2025 | Viewed by 69

Special Issue Editor


E-Mail Website
Guest Editor
Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA
Interests: DNA break repair; replication fork repair; alternative homologous end joining (alt-NHEJ); BRCA1-mutant cancers

Special Issue Information

Dear Colleagues,

Chromatin remodeling is a dynamic process critically regulating many cellular events such as DNA transcription, replication, and repair through facilitating the binding of regulatory factors to specific DNA sequences. The mechanism of chromatin remodeling is dependent upon three dynamic characteristics of nucleosomes consisting of (1) reconstruction, (2) enzyme-induced covalent modification, and (3) repositioning. Chromatin remodelers, which are large chromatin-remodeling complexes, utilize ATP hydrolysis to alter nucleosome composition and chromatin packaging; this creates open chromatin structures that allow access to DNA repair proteins, which necessitate DNA damage repairs (DDRs) and DNA repair pathway choice. For instance, chromatin remodelers, typically ATPase-dependent complexes, can collaborate with epigenetic readers or modifying enzymes in an acetylation- or poly(ADP-ribosyl)ation (PARylation)-dependent manner to regulate DSB repair by contributing to chromatin decompaction. On the other hand, increasing evidence suggests that DSBs can induce nucleosome remodeling. For example, following DSBs, ADP-ribosylation (ADPr) is transiently induced to augment chromatin relaxation, which enhances accessibility for DNA repair factors.

Although the functional interaction between DDRs and chromatin remodeling has been extensively studied, it is not fully elucidated. Therefore, this Special Issue aims to further explore the novel mechanisms underlying how chromatin remodeling regulates DDRs and how DDRs regulate chromatin remodeling.

We welcome original research papers, comprehensive reviews, and/or letters that shed light on the mechanisms elucidating the functional interactions between chromatin remodeling and DDRs.  

Dr. Manh Tien Tran
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Genes is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • chromatin remodeling
  • chromatin remodelers
  • nucleosome
  • histone modification
  • DNA damage responses

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue policies can be found here.

Published Papers

This special issue is now open for submission.
Back to TopTop