A Review of mTOR Pathway Inhibitors in Gynecologic Cancer

被引:48
作者
de Melo, Andreia Cristina [1 ]
Paulino, Eduardo [1 ]
Ingles Garces, Alvaro Henrique [1 ]
机构
[1] Brazilian Natl Canc Inst INCA, Rio De Janeiro, RJ, Brazil
关键词
PHASE-II TRIAL; RECURRENT EPITHELIAL OVARIAN; ENDOMETRIAL CANCER; PI3K/AKT/MTOR PATHWAY; OPEN-LABEL; LIPOSOMAL DOXORUBICIN; HUMAN-PAPILLOMAVIRUS; THERAPEUTIC TARGET; MAMMALIAN TARGET; GROWTH-FACTOR;
D O I
10.1155/2017/4809751
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The treatment of advanced gynecologic cancers remains palliative in most of cases. Although systemic treatment has entered into the era of targeted drugs the antitumor efficacies of current therapies are still limited. In this context there is a great need for more active treatment and rationally designed targeted therapies. The PI3K/AKT/mTOR is a signaling pathway in mammal cells that coordinates important cell activities. It has a critical function in the survival, growth, and proliferation of malignant cells and was object of important research in the last two decades. The mTOR pathway emerges as an attractive therapeutic target in cancer because it serves as a convergence point formany growth stimuli and, through its downstream substrates, controls cellular processes that contribute to the initiation and maintenance of cancer. Aberrant PI3K-dependent signaling occurs frequently in a wide range of tumor types, including endometrial, cervical, and ovarian cancers. The present study reviewed the available evidence regarding the potential impact of some mTOR pathway inhibitors in the treatment of gynecological cancer. Few advances in medical management have occurred in recent years in the treatment of advanced or recurrent gynecological malignancies, and a poor prognosis remains. Rationally designed molecularly targeted therapy is an emerging and important option in this setting; then more investigation in PI3K/AKT/mTOR pathway-targeted therapies is warranted.
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页数:8
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