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Published on: May 1, 2020
Role of RONS and eIFs in Cancer Progression
Yasmeen Ahmed Salaheldin1,2, Salma Sayed Mohamed Mahmoud2,3, Ebenezeri Erasto Ngowi2,4
1Department of Pathology, Faculty of Medicine, Ain Shams University, Cairo 11517, Egypt.
Oxidative stress from reactive oxygen and nitrogen species (RONS) and dysregulated eukaryotic translation initiation factors (eIFs) have dual roles in cancer. This review explores their complex links to cancer signaling pathways like MAPK and PI3K.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Conflicting evidence exists regarding the role of oxidative stress in cancer.
- Reactive oxygen and nitrogen species (RONS) can promote or inhibit cancer progression.
- Eukaryotic translation initiation factors (eIFs) are crucial in cellular transformation and tumorigenesis, with their dysregulation linked to cancer progression.
Purpose of the Study:
- To review and summarize recent findings on the link between oxidative stress, RONS, and eIFs in cancer.
- To explore the connection between these factors and cancer-related signaling pathways.
- To highlight potential therapeutic molecular targets for improved cancer treatment.
Main Methods:
- Literature review of recent scientific findings.
- Analysis of studies linking RONS and eIFs to cancer development.
- Examination of connections to signaling pathways such as MAPK and PI3K.
Main Results:
- RONS exhibit a dual role, potentially promoting cancer initiation or mitigating progression.
- Dysregulated eIFs are associated with altered cancer cell survival, metastasis, and angiogenesis.
- Evidence increasingly links oxidative stress and eIFs to cancer-related signaling pathways.
Conclusions:
- Oxidative stress and eIFs are intricately involved in cancer development.
- Targeting RONS and eIFs presents a promising avenue for novel cancer therapies.
- Further research is needed to harness these factors for improved anticancer drug efficacy and reduced side effects.
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