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The role of CIP2A in cancer: A review and update
Saiedeh Razi Soofiyani1, Mohammad Saeid Hejazi2, Behzad Baradaran3
1Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Molecular Medicine, Faculty of Advanced Biomedical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Abstract:
Cancerous inhibitor of protein phosphatase 2A (CIP2A) is a characterized human oncoprotein that is able to promote cancer cells proliferation, anchorage-independent cell growth and resistance to apoptosis. CIP2A inactivates protein phosphatase 2A (PP2A) which down-regulates Akt (Protein Kinase B) phosphorylation and stabilizes c-Myc (c-Myc oncogene product) in cancer cells. CIP2A has been studied in the most of human malignancies. Here we discuss the role of CIP2A in cancer and give a summary of CIP2A expression in malignancies. Also, where available we indicated the association of CIP2A with the stage of cancers and patients prognosis, explain its localization and the possibility of targeting CIP2A in different cancers.
Insights
Cancerous inhibitor of protein phosphatase 2A (CIP2A) promotes cancer growth by inactivating PP2A, stabilizing c-Myc, and upregulating Akt. Targeting CIP2A offers a potential therapeutic strategy across various human malignancies.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cancerous inhibitor of protein phosphatase 2A (CIP2A) is a human oncoprotein.
- CIP2A promotes cancer cell proliferation, anchorage-independent growth, and resistance to apoptosis.
- CIP2A functions by inactivating protein phosphatase 2A (PP2A).
Purpose of the Study:
- To discuss the role of CIP2A in human malignancies.
- To summarize CIP2A expression patterns in various cancers.
- To explore CIP2A's association with cancer stage, patient prognosis, and its therapeutic targeting potential.
Main Methods:
- Literature review and data synthesis on CIP2A.
- Analysis of CIP2A expression in human cancers.
- Examination of CIP2A's functional mechanisms and localization.
- Review of potential therapeutic strategies targeting CIP2A.
Main Results:
- CIP2A inactivates PP2A, leading to decreased Akt phosphorylation and increased c-Myc stabilization.
- CIP2A expression is observed in most human malignancies.
- CIP2A's association with cancer stage, prognosis, and localization varies across different cancer types.
- CIP2A presents a potential therapeutic target in multiple cancers.
Conclusions:
- CIP2A is a significant oncoprotein implicated in cancer progression through PP2A/Akt/c-Myc pathway.
- Understanding CIP2A expression and its correlation with clinical outcomes is crucial.
- Targeting CIP2A holds promise for novel cancer therapies.
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