The DOI matches its Crossref record; 109 of the 109 references it cites were found in a registry or an index.
Proline Metabolism and Microenvironmental Stress
Open accessAbstract
Proline, the only proteinogenic secondary amino acid, is metabolized by its own family of enzymes responding to metabolic stress and participating in metabolic signaling. Collagen in extracellular matrix, connective tissue, and bone is an abundant reservoir for proline. Matrix metalloproteinases degrading collagen are activated during stress to make proline available, and proline oxidase, the first enzyme in proline degradation, is induced by p53, peroxisome proliferator-activated receptor γ (PPARγ) and its ligands, and by AMP-activated protein kinase downregulating mTOR. Metabolism of proline generates electrons to produce ROS and initiates a variety of downstream effects, including blockade of the cell cycle, autophagy, and apoptosis. The electrons can also enter the electron transport chain to produce adenosine triphosphate for survival under nutrient stress. Pyrroline-5-carboxylate, the product of proline oxidation, is recycled back to proline with redox transfers or is sequentially converted to glutamate and alpha-ketoglutarate. The latter augments the prolyl hydroxylation of hypoxia-inducible factor-1α and its proteasomal degradation. These effects of proline oxidase, as well as its decreased levels in tumors, support its role as a tumor suppressor. The mechanism for its decrease is mediated by a specific microRNA. The metabolic signaling by proline oxidase between oxidized low-density lipoproteins and autophagy provides a functional link between obesity and increased cancer risk.
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Cellular Metabolic Stress: Considering How Cells Respond to Nutrient Excess
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Proline-dependent regulation of collagen metabolism
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Sex and APOE ε4 genotype modify the Alzheimer’s disease serum metabolome
Arnold, M., Nho, K., Kueider-Paisley, A., Massaro, T., Huynh, K., Brauner, B., MahmoudianDehkordi, S., Louie, G., Moseley, M. A., Thompson, J. W., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14959-w · Cited by 202
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Clavijo-Cornejo, D., Martínez-Flores, K., Silva-Luna, K., Martínez-Nava, G. A., Fernández-Torres, J., Zamudio-Cuevas, Y., Guadalupe Santamaría-Olmedo, M., Granados-Montiel, J., Pineda, C., & López-Reyes, A. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/1472567 · Cited by 65
Metadata
- Authors
- Phang, J. M., Liu, W., & Zabirnyk, O.
- Venue
- Annual Review of Nutrition
- Publisher
- Annual Reviews
- Published
- 2010-07-01
- Volume
- 30
- Issue
- 1
- Pages
- 441-463
- ISSN
- 0199-9885 (ISSN-L)
- 1545-4312
- OpenAlex
- W2133872445
- Cited by
- 304
- References
- 109
- FWCI
- 0.72
- Type
- journal article
- Language
- en
- Open access
- green
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