• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

头颈部鳞状细胞癌的新药研发:PI3-K抑制剂

New drug development in head and neck squamous cell carcinoma: The PI3-K inhibitors.

作者信息

De Felice Francesca, Guerrero Urbano Teresa

机构信息

Department of Radiotherapy, Policlinico Umberto I, "Sapienza" University of Rome, Rome, Italy.

Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

出版信息

Oral Oncol. 2017 Apr;67:119-123. doi: 10.1016/j.oraloncology.2017.02.020. Epub 2017 Feb 27.

DOI:10.1016/j.oraloncology.2017.02.020
PMID:28351565
Abstract

Over the last few years a number of new different compounds have been developed. They include phosphatidylinositol 3-kinase (PI3-K) inhibitors. Deregulation within the PI3-K pathway is common in head neck squamous cell carcinoma (HNSCC) and it represents a growing area of research. PI3-K inhibitors, including BKM120, PX-866 and BYL719, are being tested in several phase I and phase II studies in patients with locally advanced, recurrent or metastatic disease. This review provides an update of published clinical trials and highlights the challenges of PI3-K inhibitors in HNSCC.

摘要

在过去几年中,已经开发出了许多新型不同化合物。其中包括磷脂酰肌醇3激酶(PI3-K)抑制剂。PI3-K信号通路失调在头颈部鳞状细胞癌(HNSCC)中很常见,并且它是一个不断发展的研究领域。包括BKM120、PX-866和BYL719在内的PI3-K抑制剂正在针对局部晚期、复发或转移性疾病患者进行多项I期和II期研究测试。本综述提供了已发表临床试验的最新情况,并强调了PI3-K抑制剂在HNSCC治疗中的挑战。

相似文献

1
New drug development in head and neck squamous cell carcinoma: The PI3-K inhibitors.头颈部鳞状细胞癌的新药研发:PI3-K抑制剂
Oral Oncol. 2017 Apr;67:119-123. doi: 10.1016/j.oraloncology.2017.02.020. Epub 2017 Feb 27.
2
ERK-dependent IL-6 autocrine signaling mediates adaptive resistance to pan-PI3K inhibitor BKM120 in head and neck squamous cell carcinoma.ERK 依赖性的 IL-6 自分泌信号转导介导了头颈部鳞状细胞癌对泛 PI3K 抑制剂 BKM120 的适应性耐药。
Oncogene. 2018 Jan 18;37(3):377-388. doi: 10.1038/onc.2017.339. Epub 2017 Sep 25.
3
Dysregulations in the PI3K pathway and targeted therapies for head and neck squamous cell carcinoma.PI3K通路失调与头颈部鳞状细胞癌的靶向治疗
Oncotarget. 2017 Mar 28;8(13):22203-22217. doi: 10.18632/oncotarget.14729.
4
PI3k inhibitors (BKM120 and BYL719) as radiosensitizers for head and neck squamous cell carcinoma during radiotherapy.PI3K 抑制剂(BKM120 和 BYL719)作为放疗期间头颈部鳞状细胞癌的放射增敏剂。
PLoS One. 2021 Jan 20;16(1):e0245715. doi: 10.1371/journal.pone.0245715. eCollection 2021.
5
Current Role of Dacomitinib in Head and Neck Cancer.达可替尼在头颈癌中的当前作用
Expert Opin Investig Drugs. 2016 Jun;25(6):735-42. doi: 10.1080/13543784.2016.1177022. Epub 2016 May 3.
6
Activation of the PI3-K/AKT pathway and implications for radioresistance mechanisms in head and neck cancer.PI3-K/AKT通路的激活及其在头颈癌放射抵抗机制中的意义
Lancet Oncol. 2008 Mar;9(3):288-96. doi: 10.1016/S1470-2045(08)70073-1.
7
Molecular targeted therapies in the management of head and neck squamous cell carcinoma: recent developments and perspectives.头颈部鳞状细胞癌的分子靶向治疗:最新进展和展望。
Anticancer Agents Med Chem. 2013 Mar;13(3):389-402.
8
Deguelin Potentiates Apoptotic Activity of an EGFR Tyrosine Kinase Inhibitor (AG1478) in PIK3CA-Mutated Head and Neck Squamous Cell Carcinoma.鱼藤素增强PIK3CA突变的头颈部鳞状细胞癌中表皮生长因子受体酪氨酸激酶抑制剂(AG1478)的凋亡活性。
Int J Mol Sci. 2017 Jan 26;18(2):262. doi: 10.3390/ijms18020262.
9
Targeting EGFR-PI3K-AKT-mTOR signaling enhances radiosensitivity in head and neck squamous cell carcinoma.靶向表皮生长因子受体-磷脂酰肌醇-3-激酶-蛋白激酶B-哺乳动物雷帕霉素靶蛋白信号通路可增强头颈部鳞状细胞癌的放射敏感性。
Expert Opin Ther Targets. 2015 Jun;19(6):795-805. doi: 10.1517/14728222.2015.1012157. Epub 2015 Feb 5.
10
Phosphorylation of AKT(Ser473) serves as an independent prognostic marker for radiosensitivity in advanced head and neck squamous cell carcinoma.AKT(丝氨酸473)的磷酸化作为晚期头颈部鳞状细胞癌放射敏感性的独立预后标志物。
Int J Cancer. 2015 Jun 15;136(12):2775-85. doi: 10.1002/ijc.29328. Epub 2014 Nov 26.

引用本文的文献

1
Effect of deubiquitinases in head and neck squamous cell carcinoma (Review).去泛素化酶在头颈部鳞状细胞癌中的作用(综述)
Oncol Lett. 2025 Apr 23;29(6):307. doi: 10.3892/ol.2025.15053. eCollection 2025 Jun.
2
Radiotherapy and Systemic Therapies: Focus on Head and Neck Cancer.放射治疗与全身治疗:聚焦头颈癌
Cancers (Basel). 2023 Aug 24;15(17):4232. doi: 10.3390/cancers15174232.
3
Prognostic value of the , , and mutations in oral squamous cell carcinoma: literature review.口腔鳞状细胞癌中 、 和 突变的预后价值:文献综述
Arch Med Sci. 2020 Nov 13;17(1):207-217. doi: 10.5114/aoms.2020.100780. eCollection 2021.
4
Repression of AXL expression by AP-1/JNK blockage overcomes resistance to PI3Ka therapy.阻断 AP-1/JNK 抑制 AXL 的表达可克服对 PI3Ka 治疗的耐药性。
JCI Insight. 2019 Mar 12;5(8):125341. doi: 10.1172/jci.insight.125341.
5
Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets.头颈部鳞状细胞癌中表皮生长因子受体(EGFR)靶向治疗之外:血管生成、磷脂酰肌醇-3激酶(PI3K)及其他分子靶点
Front Oncol. 2019 Feb 13;9:74. doi: 10.3389/fonc.2019.00074. eCollection 2019.
6
Evidence mapping and quality assessment of systematic reviews on therapeutic interventions for oral cancer.口腔癌治疗干预系统评价的证据图谱与质量评估
Cancer Manag Res. 2018 Dec 24;11:117-130. doi: 10.2147/CMAR.S186700. eCollection 2019.
7
An update: emerging drugs to treat squamous cell carcinomas of the head and neck.更新:治疗头颈部鳞状细胞癌的新兴药物。
Expert Opin Emerg Drugs. 2018 Dec;23(4):283-299. doi: 10.1080/14728214.2018.1543400. Epub 2018 Nov 16.
8
Primary Epithelioid Angiosarcoma of the Thyroid in a Patient Occupationally Exposed to Radiations.一名职业性接触辐射的患者的甲状腺原发性上皮样血管肉瘤
Front Endocrinol (Lausanne). 2018 Oct 1;9:577. doi: 10.3389/fendo.2018.00577. eCollection 2018.
9
Synthesis and PI3 Kinase Inhibition Activity of Some Novel Trisubstituted Morpholinopyrimidines.一些新型三取代吗啉嘧啶的合成及对 PI3 激酶的抑制活性。
Molecules. 2018 Jul 10;23(7):1675. doi: 10.3390/molecules23071675.
10
Synthesis and PI 3-Kinase Inhibition Activity of Some Novel 2,4,6-Trisubstituted 1,3,5-Triazines.一些新型 2,4,6-三取代-1,3,5-三嗪的合成及对 PI3K 的抑制活性。
Molecules. 2018 Jul 4;23(7):1628. doi: 10.3390/molecules23071628.