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ROS signalling in the biology of cancer
Jennifer N Moloney1, Thomas G Cotter1
1Tumour Biology Laboratory, School of Biochemistry and Cell Biology, Bioscience Research Institute, University College Cork, Cork, Ireland.
Abstract:
Increased reactive oxygen species (ROS) production has been detected in various cancers and has been shown to have several roles, for example, they can activate pro-tumourigenic signalling, enhance cell survival and proliferation, and drive DNA damage and genetic instability. Counterintuitively ROS can also promote anti-tumourigenic signalling, initiating oxidative stress-induced tumour cell death. Tumour cells express elevated levels of antioxidant proteins to detoxify elevated ROS levels, establish a redox balance, while maintaining pro-tumourigenic signalling and resistance to apoptosis. Tumour cells have an altered redox balance to that of their normal counterparts and this identifies ROS manipulation as a potential target for cancer therapies. This review discusses the generation and sources of ROS within tumour cells, the regulation of ROS by antioxidant defence systems, as well as the effect of elevated ROS production on their signalling targets in cancer. It also provides an insight into how pro- and anti-tumourigenic ROS signalling pathways could be manipulated in the treatment of cancer.
Insights
Reactive oxygen species (ROS) play dual roles in cancer, promoting tumor growth and cell death. Targeting ROS offers a promising therapeutic strategy for cancer treatment by manipulating these pathways.
Area of Science:
- Oncology
- Biochemistry
- Cell Biology
Background:
- Increased reactive oxygen species (ROS) production is a hallmark of cancer, influencing tumor progression and survival.
- Tumor cells maintain altered redox balance by upregulating antioxidant systems to support pro-tumourigenic signaling and evade apoptosis.
Purpose of the Study:
- To review the generation, sources, and regulation of ROS in cancer cells.
- To explore the dual pro- and anti-tumourigenic roles of ROS signaling.
- To provide insights into manipulating ROS pathways for cancer therapy.
Main Methods:
- Literature review of ROS generation, antioxidant systems, and signaling pathways in cancer.
- Analysis of the dual role of ROS in promoting tumor growth and inducing cell death.
- Discussion of therapeutic strategies targeting ROS in cancer treatment.
Main Results:
- ROS can activate pro-tumourigenic signaling, enhance cell survival, and drive DNA damage.
- ROS also initiate anti-tumourigenic signaling, leading to oxidative stress-induced tumor cell death.
- Tumor cells' altered redox balance presents a therapeutic vulnerability.
Conclusions:
- ROS are critical mediators in cancer, with both tumor-promoting and tumor-suppressing effects.
- Targeting the redox balance in cancer cells by manipulating ROS is a viable therapeutic approach.
- Further research into ROS signaling pathways can lead to novel cancer treatment strategies.
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