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Relationship: 2813
Title
Energy Deposition leads to Increase, Oxidative DNA damage
Upstream event
Downstream event
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| Deposition of energy leading to occurrence of cataracts | non-adjacent | Moderate | Moderate | Arthur Author (send email) | Open for citation & comment |
Taxonomic Applicability
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | Moderate |
Life Stage Applicability
| Term | Evidence |
|---|---|
| All life stages | Low |
Energy can be deposited onto biomolecules stochastically from various forms of radiation. As radiation passes through an organism, it loses energy; potentially causing direct and indirect molecular-level damage in the process. The extent of damage occurs at various levels depending on ionization and non-ionization events (excitation of molecules). Reaction with water molecules can produce reactive oxygen species (ROS). Additionally, enzymes involved in reactive oxygen and nitrogen species (RONS) production can be directly upregulated (de Jager, Cockrell & Plessis, 2017). When one ROS interacts with the DNA, it produces DNA-protein cross-links, inter and intra-strand links, and tandem base lesions. When at least two ROS associate with DNA it produces oxidatively generated clustered DNA lesions (OCDLs), more complex damage. This can include single and double strand breaks, abasic sites, and oxidized bases (Cadet et al., 2012), which can lead to chromosomal aberrations, cytotoxicity, and oncogenic transformations (Stohs, 1995) as well as structural changes to the DNA, blocking polymerases (Zhang et al., 2010). Cells contain DNA repair mechanisms that help lessen the damage, but they are not perfect and can lead to insufficient repair , resulting in sustained damage (Eaton, 1995; Ainsbury et al., 2016; Markkanen, 2017).
The strategy for collating the evidence to support the relationship is described in Kozbenko et al 2022. Briefly, a scoping review methodology was used to prioritize studies based on a population, exposure, outcome, endpoint statement.
| ID | Experimental Design | Species | Upstream Observation | Downstream Observation | Citation (first author, year) | Notes |
|---|
| Title | First Author | Biological Plausibility |
Dose Concordance |
Temporal Concordance |
Incidence Concordance |
|---|
Biological Plausibility
Dose Concordance Evidence
Temporal Concordance Evidence
Incidence Concordance Evidence
Uncertainties and Inconsistencies
There are several uncertainties for this KER.
- Some of the data indicates that oxidative DNA damage increases as the time since exposure (Pendergrass et al., 2010; Mesa and Bassnett, 2013). However, other data found a very slight decrease (Mesa and Bassnett, 2013).
- Certain studies found that doses less than 0.5 Gy decrease ROS levels in a non-significant manner. This is thought to be due to radio-tolerance, where low doses induce defense mechanisms, such as glutathione or superoxide dismutase. As the dose is low, these defenses can overcome the effects of radiation, but as doses increase, they become overwhelmed, leading to increases in ROS levels (Bahia et al., 2018). These changes subsequently cause a similar pattern in DNA oxidative damage that dips between 0 and 0.5 Gy, where it begins to slowly increase (Bahia et al., 2018; Cheng et al., 2019).
| Modulating Factor (MF) | MF Specification | Effect(s) on the KER | Reference(s) |
|---|---|---|---|
| Antioxidants | Increased concentration, examples of antioxidants studied include glutathione and superoxide dismutase | Antioxidants scavenge ROS, resulting in a decrease in oxidative DNA damage. | Pendergrass et al., 2010; Bahia et al., 2018 |
| UV absorbing contact lenses | Examples include senofilcon A | Helps to protect the eye against high doses of UVA, therefore decreasing oxidative DNA damage. | Giblin et al., 2012 |
| Xeroderma pigmentosum | Presence of the genetic condition | Increases sensitivity to UV-induced oxidative DNA damage by affecting the nucleotide excision repair system. | Di Girolamo, 2010 |
| lncRNA H19 | Knockdown of lncRNA H19 | Increases sensitivity to UVB-induced oxidative DNA damage by affecting the nucleotide excision repair system. | Cheng et al., 2019 |
| Low radiation doses | Radiotolerance | Cells may display radio-tolerance by activating ROS scavenger defense mechanisms at low doses, resulting in a decrease in ROS levels and therefore a decrease in oxidative DNA damage, compared to the control. However, at higher doses these defenses are overwhelmed, and ROS levels rise. | Bahia et al., 2018 |
| Replication rate | Increased replication | Cells that are actively replicating have increased rates of photolesion repair, and therefore, lower rates of oxidative DNA damage, as opposed to quiescent cells. | Mesa & Bassnett, 2013 |
The following tables provide representative examples of the relationship, unless otherwise indicated, all data is statistically significant.
Dose Concordance
|
Reference |
Experiment Description |
Result |
|
Bahia et al., 2018 |
In vitro. Human lens epithelial cells were exposed to X rays at either 1.62 cGy/min or 38.2 cGy/min. 20 min HPLC-CoulArray analysis was used to determine 8-hydroxy deoxyguanosine (8-OH-DG) concentration. |
Human LECs exposed to 0 – 5 Gy X-rays displayed a gradual increase in 8-OH-DG concentration, reaching 2.25x control at the maximum dose. |
|
Cheng et al., 2019 |
In vitro. Human SRA01/04 lens epithelial cells exposed to UVB (312 nm peak, 280-320 nm range), the 8-OHdG ELISA assay was used to measure the amount of 8-OHdG present. |
In cells exposed to UVB, the addition of siRNA2, a type of H19-siRNA, caused a 1.2x increase in 8-OHdG relative to control. Similarly, the addition of H19 into a pcDNA vector caused a 1.25x decrease in 8-OHdG relative to control. |
Incidence Concordance
No data found.
Time Concordance
|
Reference |
Experiment Description |
Result |
|
Pendergrass et al., 2010 |
In vivo. Female, adult, C57BL/6 mouse lenses received whole-body irradiation with 11 Gy X-rays at 2 Gy/min. Immunofluorescence was then used to determine the number of 8-OH-dG positive cortical nuclear fragments beneath the central zone. |
In mice lenses immediately exposed in vivo to 11 Gy X-rays the level of 8-OH G positive DNA fragments increased to 3.5x control 9.5 months post-irradiation. |
Response-response Relationship
As the time since irradiation increases, damage levels slowly increase during the first few months, but begin to rise more quickly as time passes (Pendergrass et al., 2010; Mesa and Bassnett, 2013).
Time-scale
Known Feedforward/Feedback loops influencing this KER
N/A
This KER is plausible in all life stages, sexes, and organisms with DNA. The majority of the evidence is from in vivo female mice and rabbits, and female human and mice in vitro models.