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Relationship: 3094
Title
Alteration, lipid metabolism leads to General Apoptosis
Upstream event
Downstream event
Key Event Relationship Overview
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| Reactive Oxygen (ROS) formation leads to cancer via Peroxisome proliferation-activated receptor (PPAR) pathway | adjacent | High | Not Specified | John Frisch (send email) | Under development: Not open for comment. Do not cite |
Taxonomic Applicability
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | High |
Life Stage Applicability
| Term | Evidence |
|---|---|
| All life stages | High |
Key Event Relationship Description
Alteration of lipid metabolism leads to changes in cell lipid levels, structural changes in membranes (lipids are key components), and changes in signaling pathways affecting gene and protein expression (Huang and Freter, 2015). Loss of plasma membrane integrity due to disruptions to lipid metabolism results in cellular processes identifying cells as damaged, triggering apoptosis pathways. Oxidation of fatty acids can lead to increases of reactive oxygen species (ROS), creating an additional stress disrupting the cellular environment. As lipids represent a diverse class of molecules, and the basic building blocks for many biologically important compounds, disruption of lipid function will eventually lead to damaged cells and cell death via apoptosis.
Evidence Collection Strategy
This KER was identified as part of an Environmental Protection Agency effort to represent putative AOPs from peer-reviewed literature which were heretofore unrepresented in the AOP-Wiki. Support for this KER is referenced in publications cited in the originating work of Jeong and Choi (2020).
Evidence Supporting this KER
Biological Plausibility
The biological plausibility linking alterations in lipid metabolism to apoptosis is moderate. Disruption of lipid metabolism via stressors has been shown to lead to apoptosis, particularly through resulting loss of plasma membrane integrity.
Empirical Evidence
See Huang and Freter (2015) for review of the relationship between lipid metabolism and apoptosis.
|
Species |
Duration |
Dose |
Alteration lipid metabolism? |
General Apoptosis? |
Summary |
Citation |
|
Lab rats (Rattus norvegicus) |
4 hours |
Injection exposure of methamphetamine. |
Yes |
Yes |
In rats, methamphetamine exposure induced expression genes that control lipid metabolism and apoptosis. |
Cadet et al. (2010) |
|
Human (Homo sapiens) |
48 hours |
In vitro exposure of 50-300 uM CPI-613. |
Yes |
Yes |
Human pancreatic cells exposed to PPAR antagonist compounds repressed lipid metabolism and triggered apoptosis. |
Gao et al. (2020) |
|
Mussel (Mytilus galloprovincialis) |
7 days |
Aquatic exposure of 0.5, 5, 50 ug/L of <100, 100-1000 um polyethylene and polystyrene microplastics |
Yes |
Yes |
Mussels showed altered gene expression of genes associated with lipid metabolism and apoptosis. |
Avio et al. (2015) |
Uncertainties and Inconsistencies
Known modulating factors
Quantitative Understanding of the Linkage
Response-response Relationship
Time-scale
Known Feedforward/Feedback loops influencing this KER
Domain of Applicability
Life Stage: The life stage applicable to this key event relationship is all life stages.
Sex: This key event relationship applies to both males and females.
Taxonomic: This key event relationship appears to be present broadly, with representative studies on mammals (humans, lab mice, lab rats).
References
Avio, C.G., Gorbi, S., Milan, M., Benedetti, M., Fattorini, D., D’Errico, G., Pauletto, M., Bargelloni, L., and Regoli, F. 2015. Pollutants bioavailability and toxicological risk from microplastics to marine mussels. Environmental Pollutants 198: 211-222.
Cadet, J.L., Jayanthi, S., McCoy, M.T., Beauvais, G., and Cai, N.S. 2010. Dopamine D1 receptors, regulation of gene expression in the brain, and neurogeneration. CNS Neurological Disorders - Drug Targets 9: 526-538.
Gao, L., Xu, Z., Huang, Z., Tang, Y., Yang, D., Huang, J., He, L., Liu, M., Chen, Z., and Teng, Y. 2020. CPI-613 rewires lipid metabolism to enhance pancreatic cancer apoptosis via the AMPK-ACC signaling. 39: 73.
Huang, C. and Freter, C. 2015. Lipid metabolism, apoptosis and cancer therapy. International Journal of Molecular Sciences 16: 924-949.