Nonhomologous DNA end joining (NHEJ) is the major DNA double‐strand break (DSB) repair pathway in mammals. Previously, we have described a small molecule inhibitor, SCR …
U Ray, SK Raul, VK Gopinatha, D Ghosh… - Molecular …, 2020 - Wiley Online Library
Targeting DNA repair with small‐molecule inhibitors is an attractive strategy for cancer therapy. Majority of DNA double‐strand breaks in mammalian cells are repaired through …
E Pastwa, M Malinowski - Current cancer drug targets, 2007 - benthamdirect.com
Non-homologous DNA end joining (NHEJ) is the major pathway for the repair of double- strand breaks (DSBs) in human cells. Proteins involved in NHEJ pathway can become …
Aim: Mammalian DNA Ligases play pivotal role in processes such as DNA replication, recombination, and repair, which qualifies them as potent therapeutic targets to eradicate …
V Gopalakrishnan, G Radha… - Journal of Radiation …, 2018 - journals.lww.com
Aim: Diffuse large B-cell lymphoma (DLBCL) is the most common and aggressive type of non-Hodgkin's lymphoma that accounts for~ 40% of all lymphomas. DLBCL is considered to …
Background DNA double‐strand breaks (DSBs) are harmful to the cell as it could lead to genomic instability and cell death when left unrepaired. Homologous recombination and …
J Du, F Chen, J Yu, L Jiang, M Zhou - Molecular Cancer Research, 2021 - AACR
As the predominant pathway for the repair of DNA double-strand breaks (DSB), non- homologous end joining (NHEJ) attenuates the efficacy of cancer treatment which relies on …
DNA Ligase IV is responsible for sealing of double-strand breaks (DSBs) during nonhomologous end-joining (NHEJ). Inhibiting Ligase IV could result in amassing of DSBs …
U Ray, VK Gopinatha, S Sharma, L Goyary… - The FEBS …, 2023 - Wiley Online Library
Mercaptopyrimidine derivatives are heterocyclic compounds with potent biological activities including antiproliferative, antibacterial, and anti‐inflammatory properties. The present study …