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Protein Phosphorylation in Cancer: Role of Nitric Oxide Signaling Pathway
Xinran Liu1,2, Yiping Zhang1,2, Yijie Wang1,2
1Department of Physiology, College of Medicine, Nanchang University, Nanchang 330006, China.
Abstract:
Nitric oxide (NO), a free radical, plays a critical role in a wide range of physiological and pathological processes. Due to its pleiotropic function, it has been widely investigated in various types of cancers and is strongly associated with cancer development. Mounting pieces of evidence show that NO regulates various cancer-related events, which mainly depends on phosphorylating the key proteins in several signaling pathways. However, phosphorylation of proteins modulated by NO signaling pathway may lead to different effects in different types of cancer, which is complex and remains unclear. Therefore, in this review, we focus on the effect of protein phosphorylation modulated by NO signaling pathway in different types of cancers including breast cancer, lung cancer, prostate cancer, colon cancer, gastric cancer, pancreatic cancer, ovarian cancer, and neuroblastoma. Phosphorylation of key proteins, including p38 MAPK, ERK, PI3K, STAT3, and p53, modified by NO in various signaling pathways affects different cancer-related processes including cell apoptosis, proliferation, angiogenesis, metastasis, and several cancer therapies. Our review links the NO signaling pathway to protein phosphorylation in cancer development and provides new insight into potential targets and cancer therapy.
Insights
Nitric oxide (NO) influences cancer by altering protein phosphorylation in key signaling pathways. This review explores NO
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Nitric oxide (NO) is a crucial free radical involved in numerous physiological and pathological processes.
- Its diverse functions have led to extensive research in various cancers, highlighting its strong association with cancer development.
- NO's regulation of cancer-related events primarily occurs through the phosphorylation of key proteins in signaling pathways.
Purpose of the Study:
- To review the complex role of protein phosphorylation modulated by the nitric oxide (NO) signaling pathway in diverse cancer types.
- To elucidate how NO-mediated phosphorylation impacts cancer development and progression across different malignancies.
- To provide insights into potential therapeutic targets and strategies for cancer treatment.
Main Methods:
- Literature review focusing on studies investigating nitric oxide (NO) signaling.
- Analysis of research on protein phosphorylation in various cancers (breast, lung, prostate, colon, gastric, pancreatic, ovarian, neuroblastoma).
- Examination of the effects of NO-modulated phosphorylation on key proteins (p38 MAPK, ERK, PI3K, STAT3, p53) and cancer processes.
Main Results:
- Nitric oxide (NO) signaling modulates the phosphorylation of key proteins such as p38 MAPK, ERK, PI3K, STAT3, and p53.
- These phosphorylation events influence critical cancer-related processes including apoptosis, proliferation, angiogenesis, and metastasis.
- The effects of NO-mediated protein phosphorylation can vary significantly across different cancer types, indicating complexity.
Conclusions:
- The nitric oxide (NO) signaling pathway is intricately linked to protein phosphorylation in cancer development.
- Understanding these NO-modulated phosphorylation events offers new perspectives on cancer biology.
- This review highlights potential therapeutic targets and strategies for novel cancer therapies.
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