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Unravelling the Complexity and Functions of MTA Coregulators in Human Cancer
1Fudan University Shanghai Cancer Center and Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, China; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China; Key Laboratory of Breast Cancer in Shanghai, Shanghai Medical College, Fudan University, Shanghai, China; Key Laboratory of Epigenetics in Shanghai, Shanghai Medical College, Fudan University, Shanghai, China.
Abstract:
Since the initial recognition of the metastasis-associated protein 1 (MTA1) as a metastasis-relevant gene approximately 20 years ago, our appreciation for the complex role of the MTA family of coregulatory proteins in human cancer has profoundly grown. MTA proteins consist of six family members with similar structural units and act as central signaling nodes for integrating upstream signals into regulatory chromatin-remodeling networks, leading to regulation of gene expression in cancer cells. Substantial experimental and clinical evidence demonstrates that MTA proteins, particularly MTA1, are frequently deregulated in a wide range of human cancers. The MTA family governs cell survival, the invasive and metastatic phenotypes of cancer cells, and the aggressiveness of cancer and the prognosis of patients with MTA1 overexpressing cancers. Our discussion here highlights our current understanding of the regulatory mechanisms and functional roles of MTA proteins in cancer progression and expands upon the potential implications of MTA proteins in cancer biology and cancer therapeutics.
Insights
Metastasis-associated protein 1 (MTA1) and its family members are key regulators of gene expression in cancer. Deregulation of MTA proteins impacts cancer progression, survival, and patient prognosis, offering therapeutic potential.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Metastasis-associated protein 1 (MTA1) identified ~20 years ago.
- MTA family proteins (six members) are coregulators involved in chromatin remodeling and gene expression.
- MTA proteins are frequently deregulated in various human cancers.
Purpose of the Study:
- To review current understanding of MTA protein regulatory mechanisms in cancer.
- To discuss the functional roles of MTA proteins in cancer progression.
- To explore potential implications of MTA proteins in cancer biology and therapeutics.
Main Methods:
- Review of experimental and clinical evidence.
- Analysis of MTA protein deregulation in human cancers.
- Discussion of MTA protein functions in cell survival and metastasis.
Main Results:
- MTA proteins, especially MTA1, are frequently deregulated in diverse cancers.
- MTA family proteins regulate cell survival, invasion, and metastasis.
- MTA1 overexpression correlates with cancer aggressiveness and poorer patient prognosis.
Conclusions:
- MTA proteins are critical signaling nodes in cancer progression.
- Understanding MTA protein regulation is crucial for cancer biology.
- MTA proteins represent potential targets for novel cancer therapeutics.
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