The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Oxidative Stress and Lipid Peroxidation Products in Cancer Progression and Therapy
Open accessAbstract
The generation of reactive oxygen species (ROS) and an altered redox status are common biochemical aspects in cancer cells. ROS can react with the polyunsaturated fatty acids of lipid membranes and induce lipid peroxidation. The end products of lipid peroxidation, 4-hydroxynonenal (HNE), have been considered to be a second messenger of oxidative stress. Beyond ROS involvement in carcinogenesis, increased ROS level can inhibit tumor cell growth. Indeed, in tumors in advanced stages, a further increase of oxidative stress, such as that occurs when using several anticancer drugs and radiation therapy, can overcome the antioxidant defenses of cancer cells and drive them to apoptosis. High concentrations of HNE can also induce apoptosis in cancer cells. However, some cells escape the apoptosis induced by chemical or radiation therapy through the adaptation to intrinsic oxidative stress which confers drug resistance. This paper is focused on recent advances in the studies of the relation between oxidative stress, lipid peroxidation products, and cancer progression with particular attention to the pro-oxidant anticancer agents and the drug-resistant mechanisms, which could be modulated to obtain a better response to cancer therapy.
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Cites
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Cited by
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“Predominantly, these aggregates are made from proteins, with the remainder consisting of various lipids (Barrera, 2012; Takalo et al., 2013; Tsoukalas et al., 2019b).”
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Cell death and diseases related to oxidative stress: 4-hydroxynonenal (HNE) in the balance
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Metadata
- Authors
- Barrera, G.
- Venue
- ISRN Oncology
- Publisher
- Wiley
- Published
- 2012-10-17
- Volume
- 2012
- Pages
- 1-21
- ISSN
- 2090-5661 (ISSN-L)
- 2090-567X
- OpenAlex
- W1992782534
- Cited by
- 820
- References
- 17
- FWCI
- 19.22
- Type
- journal article
- Language
- en
- Open access
- diamond
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