Target intelligence / Profile preview

Cellular DNA Double-Strand Break Induction (DSB Induction)

Target
DSB Induction
Molecular classification
DNA Damage, Cellular Process
01

Overview

Cellular DNA double-strand break (DSB) induction refers to the creation of breaks in both strands of the DNA helix. These breaks can arise from exogenous sources like radiation and chemicals, or endogenously during DNA replication, meiosis, and immune system development. DSBs are highly cytotoxic and can lead to chromosomal instability, cell death, or tumorigenesis if not properly repaired. The DNA Damage Response (DDR) network detects and orchestrates repair through pathways like homologous recombination (HRR) and non-homologous end joining (NHEJ). Unrepaired or misrepaired DSBs can result in chromosomal rearrangements, mutations, and oncogenic translocations.

Other names
DNA Double-Strand BreaksDSBsDNA Damage Response (DDR)
02

Mechanism of action

Various mechanisms depending on the inducing agent, including direct DNA cleavage, generation of reactive oxygen species, and interference with DNA replication/repair.

03

Biological functions

DNA repairGenome maintenanceCell cycle arrestApoptosisSenescenceHomologous Recombination Repair (HRR)Non-Homologous End Joining (NHEJ)DNA Damage Response (DDR) signaling
04

Disease associations

CancerAgingImmunodeficiencyGenetic disorders
05

Safety considerations

GenotoxicityCarcinogenesisOff-target DNA damage
06

Interacting drugs

Chemotherapeutic agents (e.g., bleomycin, etoposide)

2 more in the full profile.

07

Biomarkers

γH2AX foci53BP1 fociMRE11 foci

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