When Overgrowth Bumps Into Cancer: The PTEN-Opathies

被引:101
作者
Mester, Jessica [1 ]
Eng, Charis [1 ]
机构
[1] Cleveland Clin, PTEN Cowden Multidisciplinary Clin, Cleveland, OH USA
关键词
PTEN; Cowden syndrome; AKT; PIK3CA; PI3K; mTOR; RILEY-RUVALCABA-SYNDROME; TUMOR-SUPPRESSOR GENE; AUTISM SPECTRUM DISORDERS; TUBEROUS SCLEROSIS COMPLEX; LHERMITTE-DUCLOS DISEASE; BANNAYAN-ZONANA-SYNDROME; ATP-BINDING MOTIFS; PROTEUS-SYNDROME; COWDEN-SYNDROME; MAMMALIAN TARGET;
D O I
10.1002/ajmg.c.31364
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
PTEN is a dual-specificity phosphatase and well-known tumor suppressor gene. When functioning properly, it works in its canonical pathway to inhibit AKT/mTOR and MAPK signaling, leading to cell death and growth regulation. PTEN mutations cause dysregulation of these pathways, resulting in cellular proliferation and overgrowth. When germline mutations are present as in patients with PTEN Hamartoma Tumor Syndrome (PHTS), benign and malignant neoplasias occur as well as cerebral overgrowth and neurodevelopmental abnormalities. This review article will summarize recent laboratory and clinical investigations relating to PTEN, highlighting the overgrowth aspects of this syndrome and the molecular drivers behind these key phenotypes. Finally, therapies developed targeted the PI3K/AKT/mTOR pathway for other tumor predisposition syndromes will be discussed. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:114 / 121
页数:8
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