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用于头颈癌治疗的mTOR共靶向策略。

mTOR co-targeting strategies for head and neck cancer therapy.

作者信息

Wang Zhiyong, Valera Juan Callejas, Zhao Xuefeng, Chen Qianming, Gutkind J Silvio

机构信息

Moores Cancer Center, University of California San Diego, La Jolla, CA, USA.

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases,West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, 610041, China.

出版信息

Cancer Metastasis Rev. 2017 Sep;36(3):491-502. doi: 10.1007/s10555-017-9688-7.

DOI:10.1007/s10555-017-9688-7
PMID:28822012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5613059/
Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth most common malignancy worldwide. There is an urgent need to develop effective therapeutic approaches to prevent and treat HNSCC. Recent deep sequencing of the HNSCC genomic landscape revealed a multiplicity and diversity of genetic alterations in this malignancy. Although a large variety of specific molecules were found altered in each individual tumor, they all participate in only a handful of driver signaling pathways. Among them, the PI3K/mTOR pathway is the most frequently activated, which plays a central role in cancer initiation and progression. In turn, targeting of mTOR may represent a precision therapeutic approach for HNSCC. Indeed, mTOR inhibition exerts potent anti-tumor activity in HNSCC experimental systems, and mTOR targeting clinical trials show encouraging results. However, advanced HNSCC patients may exhibit unpredictable drug resistance, and the analysis of its molecular basis suggests that co-targeting strategies may provide a more effective option. In addition, although counterintuitive, emerging evidence suggests that mTOR inhibition may enhance the anti-tumor immune response. These new findings raise the possibility that the combination of mTOR inhibitors and immune oncology agents may provide novel precision therapeutic options for HNSCC.

摘要

头颈部鳞状细胞癌(HNSCC)是全球第六大常见恶性肿瘤。迫切需要开发有效的治疗方法来预防和治疗HNSCC。最近对头颈部鳞状细胞癌基因组图谱的深度测序揭示了这种恶性肿瘤中基因改变的多样性。尽管在每个个体肿瘤中发现了大量特定分子发生改变,但它们都仅参与少数几个驱动信号通路。其中,PI3K/mTOR通路是最常被激活的,它在癌症的发生和发展中起核心作用。反过来,靶向mTOR可能代表一种针对HNSCC的精准治疗方法。事实上,mTOR抑制在HNSCC实验系统中发挥强大的抗肿瘤活性,并且靶向mTOR的临床试验显示出令人鼓舞的结果。然而,晚期HNSCC患者可能表现出不可预测的耐药性,对其分子基础的分析表明联合靶向策略可能提供更有效的选择。此外,尽管有悖常理,但新出现的证据表明mTOR抑制可能增强抗肿瘤免疫反应。这些新发现增加了mTOR抑制剂与免疫肿瘤药物联合使用可能为HNSCC提供新型精准治疗选择的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/335f/5613059/621984deb7ab/10555_2017_9688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/335f/5613059/0c6e680a9e44/10555_2017_9688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/335f/5613059/621984deb7ab/10555_2017_9688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/335f/5613059/0c6e680a9e44/10555_2017_9688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/335f/5613059/621984deb7ab/10555_2017_9688_Fig2_HTML.jpg

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