• 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

PI3K/Akt/mTOR信号通路及其在癌症治疗中的作用:我们有进展吗?

PI3K/Akt/mTOR Pathway and Its Role in Cancer Therapeutics: Are We Making Headway?

作者信息

Peng Yan, Wang Yuanyuan, Zhou Cheng, Mei Wuxuan, Zeng Changchun

机构信息

Department of Obstetrics, Longhua District Central Hospital, Shenzhen, China.

Xianning Medical College, Hubei University of Science and Technology, Xianning, China.

出版信息

Front Oncol. 2022 Mar 24;12:819128. doi: 10.3389/fonc.2022.819128. eCollection 2022.

DOI:10.3389/fonc.2022.819128
PMID:35402264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8987494/
Abstract

Cancer is a severe public health issue that is a leading cause of mortality globally. It is also an impediment to improving life expectancy worldwide. Furthermore, the global burden of cancer incidence and death is continuously growing. Current therapeutic options are insufficient for patients, and tumor complexity and heterogeneity necessitate customized medicine or targeted therapy. It is critical to identify potential cancer therapeutic targets. Aberrant activation of the PI3K/AKT/mTOR pathway has a significant role in carcinogenesis. This review summarized oncogenic PI3K/Akt/mTOR pathway alterations in cancer and various cancer hallmarks associated with the PI3K/AKT/mTOR pathway, such as cell proliferation, autophagy, apoptosis, angiogenesis, epithelial-to-mesenchymal transition (EMT), and chemoresistance. Importantly, this review provided recent advances in PI3K/AKT/mTOR inhibitor research. Overall, an in-depth understanding of the association between the PI3K/AKT/mTOR pathway and tumorigenesis and the development of therapies targeting the PI3K/AKT/mTOR pathway will help make clinical decisions.

摘要

癌症是一个严重的公共卫生问题,是全球主要的死亡原因。它也是提高全球预期寿命的一个障碍。此外,全球癌症发病率和死亡负担在持续增加。目前的治疗选择对患者来说并不充分,而且肿瘤的复杂性和异质性需要定制药物或靶向治疗。识别潜在的癌症治疗靶点至关重要。PI3K/AKT/mTOR通路的异常激活在致癌过程中起重要作用。本综述总结了癌症中致癌性PI3K/Akt/mTOR通路的改变以及与PI3K/AKT/mTOR通路相关的各种癌症特征,如细胞增殖、自噬、凋亡、血管生成、上皮-间质转化(EMT)和化疗耐药性。重要的是,本综述介绍了PI3K/AKT/mTOR抑制剂研究的最新进展。总体而言,深入了解PI3K/AKT/mTOR通路与肿瘤发生之间的关联以及开发针对PI3K/AKT/mTOR通路的疗法将有助于做出临床决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/1de21dcbb494/fonc-12-819128-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/a57f31199d43/fonc-12-819128-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/64c42aa72d3e/fonc-12-819128-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/1de21dcbb494/fonc-12-819128-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/a57f31199d43/fonc-12-819128-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/64c42aa72d3e/fonc-12-819128-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b1/8987494/1de21dcbb494/fonc-12-819128-g003.jpg

相似文献

1
PI3K/Akt/mTOR Pathway and Its Role in Cancer Therapeutics: Are We Making Headway?PI3K/Akt/mTOR信号通路及其在癌症治疗中的作用:我们有进展吗?
Front Oncol. 2022 Mar 24;12:819128. doi: 10.3389/fonc.2022.819128. eCollection 2022.
2
Inhibition of PI3K/Akt/mTOR signaling pathway alleviates ovarian cancer chemoresistance through reversing epithelial-mesenchymal transition and decreasing cancer stem cell marker expression.抑制 PI3K/Akt/mTOR 信号通路通过逆转上皮-间充质转化和降低癌症干细胞标志物表达来减轻卵巢癌的化疗耐药性。
BMC Cancer. 2019 Jun 24;19(1):618. doi: 10.1186/s12885-019-5824-9.
3
ARHGAP9 inhibits colorectal cancer cell proliferation, invasion and EMT via targeting PI3K/AKT/mTOR signaling pathway.ARHGAP9 通过靶向 PI3K/AKT/mTOR 信号通路抑制结直肠癌细胞增殖、侵袭和 EMT。
Tissue Cell. 2022 Aug;77:101817. doi: 10.1016/j.tice.2022.101817. Epub 2022 May 7.
4
The PI3K/Akt/mTOR axis in colorectal cancer: Oncogenic alterations, non-coding RNAs, therapeutic opportunities, and the emerging role of nanoparticles.结直肠癌中的PI3K/Akt/mTOR轴:致癌改变、非编码RNA、治疗机会及纳米颗粒的新作用
J Cell Physiol. 2022 Mar;237(3):1720-1752. doi: 10.1002/jcp.30655. Epub 2021 Dec 12.
5
Targeting AKT/mTOR in Oral Cancer: Mechanisms and Advances in Clinical Trials.靶向口腔癌中的 AKT/mTOR:机制与临床试验进展。
Int J Mol Sci. 2020 May 6;21(9):3285. doi: 10.3390/ijms21093285.
6
Effects of miR-202-5p silencing PIK3CA gene expression on proliferation, invasion, and epithelial-mesenchymal transition of cervical cancer SiHa cells through inhibiting PI3K/Akt/mTOR signaling pathway activation.沉默 miR-202-5p 对 PIK3CA 基因表达的影响通过抑制 PI3K/Akt/mTOR 信号通路的激活对宫颈癌 SiHa 细胞的增殖、侵袭和上皮间质转化的作用。
Mol Cell Biochem. 2021 Nov;476(11):4031-4044. doi: 10.1007/s11010-021-04211-4. Epub 2021 Jul 9.
7
Attacking the PI3K/Akt/mTOR signaling pathway for targeted therapeutic treatment in human cancer.针对人类癌症的靶向治疗,攻击 PI3K/Akt/mTOR 信号通路。
Semin Cancer Biol. 2022 Oct;85:69-94. doi: 10.1016/j.semcancer.2021.06.019. Epub 2021 Jun 25.
8
MicroRNA‑22 mediates the cisplatin resistance of osteosarcoma cells by inhibiting autophagy via the PI3K/Akt/mTOR pathway.微小 RNA-22 通过抑制自噬来介导骨肉瘤细胞对顺铂的耐药性,其作用机制是通过 PI3K/Akt/mTOR 通路。
Oncol Rep. 2020 Apr;43(4):1169-1186. doi: 10.3892/or.2020.7492. Epub 2020 Feb 7.
9
High Sensitivity of Circulating Tumor Cells Derived from a Colorectal Cancer Patient for Dual Inhibition with AKT and mTOR Inhibitors.循环肿瘤细胞衍生自结直肠癌患者,对 AKT 和 mTOR 抑制剂的双重抑制具有高敏感性。
Cells. 2020 Sep 20;9(9):2129. doi: 10.3390/cells9092129.
10
Novel approaches for molecular targeted therapy of breast cancer: interfering with PI3K/AKT/mTOR signaling.乳腺癌分子靶向治疗的新方法:干扰 PI3K/AKT/mTOR 信号通路。
Curr Cancer Drug Targets. 2013 Feb;13(2):188-204. doi: 10.2174/1568009611313020008.

引用本文的文献

1
Changes in Melanoma Cell Morphology Following Inhibition of Cell Invasion by Third-Generation mTOR Kinase Inhibitors.第三代mTOR激酶抑制剂抑制细胞侵袭后黑色素瘤细胞形态的变化
Int J Mol Sci. 2025 Aug 12;26(16):7770. doi: 10.3390/ijms26167770.
2
The Good, the Bad, or Both? Unveiling the Molecular Functions of LINC01133 in Tumors.是好、是坏,还是兼而有之?揭示LINC01133在肿瘤中的分子功能。
Noncoding RNA. 2025 Jul 30;11(4):58. doi: 10.3390/ncrna11040058.
3
Latest Advancements of Natural Products in Combating Ovarian Cancer.天然产物在对抗卵巢癌方面的最新进展

本文引用的文献

1
Role of Akt isoforms in neuronal insulin signaling and resistance.Akt 同工型在神经元胰岛素信号转导和抵抗中的作用。
Cell Mol Life Sci. 2021 Dec;78(23):7873-7898. doi: 10.1007/s00018-021-03993-6. Epub 2021 Nov 1.
2
Role of PI3K-AKT-mTOR Pathway as a Pro-Survival Signaling and Resistance-Mediating Mechanism to Therapy of Prostate Cancer.PI3K-AKT-mTOR 通路作为前列腺癌治疗中促生存信号和耐药性调节机制的作用。
Int J Mol Sci. 2021 Oct 14;22(20):11088. doi: 10.3390/ijms222011088.
3
First-in-child phase I/II study of the dual mTORC1/2 inhibitor vistusertib (AZD2014) as monotherapy and in combination with topotecan-temozolomide in children with advanced malignancies: arms E and F of the AcSé-ESMART trial.
J Cancer. 2025 Jul 28;16(11):3497-3512. doi: 10.7150/jca.118209. eCollection 2025.
4
COL1A1 drives tumor progression in kidney renal clear cell carcinoma by regulating EMT through the PI3K/Akt pathway.COL1A1通过PI3K/Akt途径调节上皮-间质转化,从而驱动肾透明细胞癌的肿瘤进展。
Cancer Cell Int. 2025 Aug 25;25(1):314. doi: 10.1186/s12935-025-03956-y.
5
Lactylation: a novel driver of drug resistance in the tumor microenvironment.乳酰化:肿瘤微环境中耐药性的新型驱动因素。
Cancer Drug Resist. 2025 Aug 4;8:39. doi: 10.20517/cdr.2025.90. eCollection 2025.
6
PI3K/Akt pathway and neuroinflammation in sepsis-associated encephalopathy.PI3K/Akt信号通路与脓毒症相关性脑病中的神经炎症
Open Med (Wars). 2025 Aug 7;20(1):20251248. doi: 10.1515/med-2025-1248. eCollection 2025.
7
Flavonoids as Promising Akt1 Inhibitors in Cancer Medicine: Insights From Molecular Docking, Dynamics, DFT Calculations, and In Vitro Validation.黄酮类化合物作为癌症医学中颇具潜力的Akt1抑制剂:来自分子对接、动力学、密度泛函理论计算及体外验证的见解
Cancer Rep (Hoboken). 2025 Aug;8(8):e70315. doi: 10.1002/cnr2.70315.
8
miRNA-204-5p acts as a tumor suppressor in gastric cancer by inhibiting cell migration, invasion, and glycolysis via the RAB22A/PI3K/AKT axis.微小RNA-204-5p通过RAB22A/PI3K/AKT轴抑制细胞迁移、侵袭和糖酵解,从而在胃癌中发挥肿瘤抑制作用。
Sci Rep. 2025 Aug 12;15(1):29536. doi: 10.1038/s41598-025-02139-z.
9
LncRNAs signatures in gynecological cancers: ovarian and endometrial cancers.妇科癌症中的长链非编码RNA特征:卵巢癌和子宫内膜癌
Clin Transl Oncol. 2025 Aug 11. doi: 10.1007/s12094-025-04020-x.
10
Impact of gastrointestinal dysbiosis on tryptophan metabolism and neurological cancer progression.胃肠道生态失调对色氨酸代谢及神经肿瘤进展的影响。
Med Oncol. 2025 Aug 6;42(9):412. doi: 10.1007/s12032-025-02972-2.
儿童晚期恶性肿瘤单药及联合拓扑替康-替莫唑胺治疗的 mTORC1/2 双重抑制剂 vistusertib(AZD2014)的首次儿童 I/II 期研究:AcSé-ESMART 试验的 E 组和 F 组。
Eur J Cancer. 2021 Nov;157:268-277. doi: 10.1016/j.ejca.2021.08.010. Epub 2021 Sep 17.
4
The Pathogenic Role of PI3K/AKT Pathway in Cancer Onset and Drug Resistance: An Updated Review.PI3K/AKT信号通路在癌症发生和耐药中的致病作用:最新综述
Cancers (Basel). 2021 Aug 5;13(16):3949. doi: 10.3390/cancers13163949.
5
Effectiveness of Adding Everolimus to the First-line Treatment of Advanced Breast Cancer in Premenopausal Women Who Experienced Disease Progression While Receiving Selective Estrogen Receptor Modulators: A Phase 2 Randomized Clinical Trial.依维莫司联合选择性雌激素受体调节剂治疗进展期绝经前女性乳腺癌的有效性:一项 2 期随机临床试验
JAMA Oncol. 2021 Oct 1;7(10):e213428. doi: 10.1001/jamaoncol.2021.3428. Epub 2021 Oct 21.
6
Targeting Akt in cancer for precision therapy.针对癌症中的 Akt 进行精准治疗。
J Hematol Oncol. 2021 Aug 21;14(1):128. doi: 10.1186/s13045-021-01137-8.
7
Phase I or II Study of Ribociclib in Combination With Topotecan-Temozolomide or Everolimus in Children With Advanced Malignancies: Arms A and B of the AcSé-ESMART Trial.Ribociclib 联合拓扑替康-替莫唑胺或依维莫司治疗晚期恶性肿瘤儿童的 I 期或 II 期研究:AcSé-ESMART 试验的 A 臂和 B 臂。
J Clin Oncol. 2021 Nov 10;39(32):3546-3560. doi: 10.1200/JCO.21.01152. Epub 2021 Aug 4.
8
Gαq activation modulates autophagy by promoting mTORC1 signaling.Gαq 的激活通过促进 mTORC1 信号来调节自噬。
Nat Commun. 2021 Jul 27;12(1):4540. doi: 10.1038/s41467-021-24811-4.
9
Targeting PI3K/AKT/mTOR Signaling Pathway in Breast Cancer.靶向乳腺癌中的PI3K/AKT/mTOR信号通路
Cancers (Basel). 2021 Jul 14;13(14):3517. doi: 10.3390/cancers13143517.
10
Targeting the PI3K/AKT/mTOR Signaling Pathway in Lung Cancer: An Update Regarding Potential Drugs and Natural Products.针对肺癌中的 PI3K/AKT/mTOR 信号通路:关于潜在药物和天然产物的最新研究。
Molecules. 2021 Jul 5;26(13):4100. doi: 10.3390/molecules26134100.