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DNA–Protein Cross-Links: Formation, Structural Identities, and Biological Outcomes

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TLDR
The chemistry of DPC formation in cells is outlined, recent efforts to identify the cross-linked proteins by mass spectrometry are described, and various methodologies for preparing DNA strands containing structurally defined, site specific DPC lesions are discussed.

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Modulating ROS to overcome multidrug resistance in cancer.

TL;DR: The critical and targetable redox-regulating enzymes, including mitochondrial electron transport chain complexes, NADPH oxidases (NOXs), enzymes related to glutathione metabolism, glutamate/cystine antiporter xCT, thioredoxin reductases (TrxRs), nuclear factor erythroid 2-related factor 2 (Nrf2), and their roles in regulating cellular ROS levels, drug resistance as well as their clinical significance are discussed.
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Reactive Oxygen Species-Related Nanoparticle Toxicity in the Biomedical Field

TL;DR: A summary of the mechanisms and responsible for ROS generation by nanoparticles at the cellular level are given and insights into the mechanics of ROS-mediated biotoxicity are provided.
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DNA damage repair: historical perspectives, mechanistic pathways and clinical translation for targeted cancer therapy.

TL;DR: Zhang et al. as discussed by the authors summarized the mechanisms regarding DNA damage repair associated with targeted cancer therapy, highlighting the specific proteins behind targeting DNA repair that initiate functioning abnormally and lead to extrinsic harm by environmental DNA damage factors, also, the DNA damage baseline drift leads to the harmful intrinsic targeted cancer therapies.
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What is the DNA repair defect underlying Fanconi anemia

TL;DR: New developments in the understanding of DPC and ICL repair are discussed, and how these findings bear on the question of which DNA lesion underlies FA are discussed.
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