原发性渗出性淋巴瘤
PI3K/AKT/mTOR通路
淋巴瘤
西罗莫司
癌症研究
mTOR抑制剂的发现与发展
细胞凋亡
医学
药理学
免疫学
化学
内科学
生物化学
作者
Carolina Caro‐Vegas,Aubrey Bailey,Riccardo Bigi,Blossom Damania,Dirk P. Dittmer
出处
期刊:MBio
[American Society for Microbiology]
日期:2019-02-18
卷期号:10 (1)
被引量:41
标识
DOI:10.1128/mbio.02871-18
摘要
Primary effusion lymphoma (PEL) is an aggressive and incurable malignancy, which is usually characterized by lymphomatous effusions in body cavities without tumor masses. PEL has no established treatment and a poor prognosis, with a median survival time shorter than 6 months. PEL usually develops in the context of immunosuppression, such as HIV infection or post-organ transplantation. The optimal treatment for PEL has not been established, as PEL is generally resistant to traditional chemotherapy. The molecular drivers for PEL are still unknown; however, PEL displays a constitutively active mammalian target of rapamycin (mTOR) pathway, which is critical for metabolic and cell survival mechanisms. Therefore, the evaluation of novel agents targeting the mTOR pathway could be clinically relevant for the treatment of PEL.
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