Essence of PTEN: a Broad-Spectrum Therapeutic Target in Cancer

被引:1
|
作者
Raghav, Mukta [1 ]
Sharma, Varruchi [2 ]
Chaudhary, Mayank [1 ]
Tuli, Hardeep Singh [1 ]
Saini, Adesh K. [1 ,3 ]
Sharma, Anil K. [1 ]
机构
[1] Maharishi Markandeshwar Deemed Be Univ, Dept Biotechnol, Mullana Ambala, Haryana, India
[2] Maharishi Markandeshwar Univ, Dept Biotechnol, Chandigarh, UT, India
[3] Maharishi Markandeshwar Univ, Kumarhatti Solan, Himachal Prades, India
来源
关键词
PTEN; Cancer; cell proliferation; Cell Cycle regulation; intracellular; cytotoxic; tumor suppression; Phosphorylation; CELL-CYCLE CONTROL; TUMOR-SUPPRESSOR; TENSIN HOMOLOG; NEGATIVE REGULATION; BREAST-CANCER; PROTEIN STABILITY; UBIQUITIN LIGASE; DOWN-REGULATION; PI3K PATHWAY; PHOSPHORYLATION;
D O I
10.33263/BRIAC112.95879603
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The levels of protein tyrosine phosphorylation within a cell is regulated by protein tyrosine kinases and protein tyrosine phosphatases. These protein tyrosine phosphatases (PTP) can act both as positive and negative regulators during cell cycle progression and signal transduction. Phosphatase activity is shown by Phosphatase and Tensin homolog (PTEN) protein encoded by PTEN gene localized on human chromosome 10. Earlier findings established the role of PTEN as a tumor suppressor in Cowden's disease, where PTEN mutations resulted in disease outcomes. Subsequent studies found the role of PTEN mutations in various human cancers, making it one of the vastly studied tumor suppressor genes. The current review has been planned to get a deeper insight into the potential role of PTEN in a variety of physiological processes involved in normal development like cell growth, migration, and differentiation along with the factors, regulation, and underlying mechanism.
引用
收藏
页码:9587 / 9603
页数:17
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