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Decoding PTEN: from biological functions to signaling pathways in tumors
Xueping Huang1, Dongyan Zhang2, Di Zhang2
1School of Stomatology, Shandong Second Medical University, Weifang, Shandong Province, PR China.
Abstract:
The tumor suppressor gene Phosphatase and tensin homologue deleted on chromosome 10 (PTEN), possessing both protein and lipid phosphatase activities, is frequently mutated in various human cancers. PTEN aberrations disrupt critical cellular processes like proliferation, apoptosis, migration, and invasion, thereby promoting tumor growth. In the cells, PTEN localizes to the nucleus, cytoplasm, or cell membrane, and its roles depends on the subcellular localization. PTEN is regulated at the transcriptional, post-transcriptional, and post-translational levels, implying that its functions on the tumors are complex. The relationship between PTEN abnormalities and tumors has garnered significant interest in recent years. PTEN regulates essential cellular processes involved in tumorigenesis. Mutations or deletions in the PTEN gene often correlate with unfavorable prognosis and increased cancer recurrence. Numerous studies suggest that PTEN expression levels in tumors could be a valuable biomarker for cancer diagnosis, treatment, and predicting patient outcomes. This paper provides a comprehensive review of the biological function, regulatory mechanisms, and post-translational modifications of PTEN. Furthermore, this review explores the expression and regulation of PTEN in different tumor types, as well as its interactions with environmental factors in tumorigenesis. This comprehensive analysis aims to deepen our understanding of the signaling pathways between PTEN and cancer.
Insights
The tumor suppressor gene PTEN is frequently altered in human cancers, impacting cell growth and survival. PTEN
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The tumor suppressor gene Phosphatase and tensin homologue deleted on chromosome 10 (PTEN) is crucial for regulating cell proliferation, apoptosis, migration, and invasion.
- Frequent mutations in PTEN are observed across various human cancers, disrupting essential cellular functions and promoting tumor growth.
- PTEN's subcellular localization (nucleus, cytoplasm, cell membrane) dictates its diverse roles in cellular processes.
Purpose of the Study:
- To provide a comprehensive review of the biological functions, regulatory mechanisms, and post-translational modifications of PTEN.
- To explore the expression and regulation of PTEN in different tumor types.
- To investigate the interactions between PTEN and environmental factors in tumorigenesis.
Main Methods:
- Literature review of PTEN's role in cancer.
- Analysis of PTEN regulation at transcriptional, post-transcriptional, and post-translational levels.
- Examination of PTEN expression and its correlation with tumor progression and patient outcomes.
Main Results:
- PTEN aberrations disrupt critical cellular processes, leading to uncontrolled proliferation and tumor development.
- Mutations or deletions in PTEN are associated with poor prognosis and increased cancer recurrence.
- PTEN expression levels show potential as a biomarker for cancer diagnosis, treatment selection, and outcome prediction.
Conclusions:
- Understanding PTEN's complex roles and regulatory networks is vital for cancer research.
- PTEN's intricate involvement in tumorigenesis highlights its significance as a therapeutic target.
- Further research into PTEN signaling pathways can deepen our comprehension of cancer development and progression.
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