• 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

蛋白磷酸酶2A癌性抑制剂(CIP2A)的致癌关联:一种多面癌蛋白

Oncogenic nexus of cancerous inhibitor of protein phosphatase 2A (CIP2A): an oncoprotein with many hands.

作者信息

De Pradip, Carlson Jennifer, Leyland-Jones Brian, Dey Nandini

机构信息

Department of Molecular and Experimental Medicine, Avera Research Institute, Sioux Falls, SD; Department of Internal Medicine, SSOM, University of South Dakota, Sioux Falls, SD.

出版信息

Oncotarget. 2014 Jul 15;5(13):4581-602. doi: 10.18632/oncotarget.2127.

DOI:10.18632/oncotarget.2127
PMID:25015035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4148086/
Abstract

Oncoprotein CIP2A a Cancerous Inhibitor of PP2A forms an "oncogenic nexus" by virtue of its control on PP2A and MYC stabilization in cancer cells. The expression and prognostic function of CIP2A in different solid tumors including colorectal carcinoma, head and neck cancers, gastric cancers, lung carcinoma, cholangiocarcinoma, esophageal cancers, pancreatic carcinoma, brain cancers, breast carcinoma, bladder cancers, ovarian carcinoma, renal cell carcinomas, tongue cancers, cervical carcinoma, prostate cancers, and oral carcinoma as well as a number of hematological malignancies are just beginning to emerge. Herein, we reviewed the recent progress in our understanding of (1) how an "oncogenic nexus" of CIP2A participates in the tumorigenic transformation of cells and (2) how we can prospect/view the clinical relevance of CIP2A in the context of cancer therapy. The review will try to understand the role of CIP2A (a) as a biomarker in cancers and evaluate the prognostic value of CIP2A in different cancers (b) as a therapeutic target in cancers and (c) in drug response and developing chemo-resistance in cancers.

摘要

癌蛋白CIP2A是一种PP2A的癌性抑制剂,通过控制癌细胞中的PP2A和MYC稳定性形成“致癌关联”。CIP2A在包括结直肠癌、头颈癌、胃癌、肺癌、胆管癌、食管癌、胰腺癌、脑癌、乳腺癌、膀胱癌、卵巢癌、肾细胞癌、舌癌、宫颈癌、前列腺癌和口腔癌在内的不同实体瘤以及一些血液系统恶性肿瘤中的表达和预后功能才刚刚开始显现。在此,我们综述了近期在理解以下两方面的进展:(1)CIP2A的“致癌关联”如何参与细胞的致瘤转化;(2)在癌症治疗背景下,我们如何展望/看待CIP2A的临床相关性。该综述将试图了解CIP2A作为(a)癌症生物标志物的作用,并评估CIP2A在不同癌症中的预后价值;(b)癌症治疗靶点的作用;以及(c)在癌症药物反应和化疗耐药性发展中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/a8441442eba0/oncotarget-05-4581-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/bdd59ec24a55/oncotarget-05-4581-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/41b04f429aa0/oncotarget-05-4581-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/f2a9601676d6/oncotarget-05-4581-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/a8441442eba0/oncotarget-05-4581-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/bdd59ec24a55/oncotarget-05-4581-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/41b04f429aa0/oncotarget-05-4581-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/f2a9601676d6/oncotarget-05-4581-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/4148086/a8441442eba0/oncotarget-05-4581-g004.jpg

相似文献

1
Oncogenic nexus of cancerous inhibitor of protein phosphatase 2A (CIP2A): an oncoprotein with many hands.蛋白磷酸酶2A癌性抑制剂(CIP2A)的致癌关联:一种多面癌蛋白
Oncotarget. 2014 Jul 15;5(13):4581-602. doi: 10.18632/oncotarget.2127.
2
CIP2A inhibits PP2A in human malignancies.CIP2A在人类恶性肿瘤中抑制蛋白磷酸酶2A(PP2A)。
Cell. 2007 Jul 13;130(1):51-62. doi: 10.1016/j.cell.2007.04.044.
3
Erlotinib derivative inhibits hepatocellular carcinoma by targeting CIP2A to reactivate protein phosphatase 2A.厄洛替尼衍生物通过靶向CIP2A重新激活蛋白磷酸酶2A来抑制肝细胞癌。
Cell Death Dis. 2014 Jul 31;5(7):e1359. doi: 10.1038/cddis.2014.325.
4
The concept of the okadaic acid class of tumor promoters is revived in endogenous protein inhibitors of protein phosphatase 2A, SET and CIP2A, in human cancers.在人类癌症中,OKADAIC 酸类肿瘤促进剂的概念在蛋白磷酸酶 2A、SET 和 CIP2A 的内源性蛋白抑制剂中得到了重现。
J Cancer Res Clin Oncol. 2018 Dec;144(12):2339-2349. doi: 10.1007/s00432-018-2765-7. Epub 2018 Oct 20.
5
Chk1 targeting reactivates PP2A tumor suppressor activity in cancer cells.chk1 靶向作用可恢复肿瘤细胞中 pp2a 肿瘤抑制子的活性。
Cancer Res. 2013 Nov 15;73(22):6757-69. doi: 10.1158/0008-5472.CAN-13-1002. Epub 2013 Sep 26.
6
Targeting SET to restore PP2A activity disrupts an oncogenic CIP2A-feedforward loop and impairs triple negative breast cancer progression.靶向 SET 以恢复 PP2A 活性会破坏致癌性 CIP2A 的正反馈回路,并损害三阴性乳腺癌的进展。
EBioMedicine. 2019 Feb;40:263-275. doi: 10.1016/j.ebiom.2018.12.032. Epub 2019 Jan 14.
7
Cucurbitacin B induces autophagy and apoptosis by suppressing CIP2A/PP2A/mTORC1 signaling axis in human cisplatin resistant gastric cancer cells.葫芦素 B 通过抑制人顺铂耐药胃癌细胞中的 CIP2A/PP2A/mTORC1 信号轴诱导自噬和细胞凋亡。
Oncol Rep. 2017 Jul;38(1):271-278. doi: 10.3892/or.2017.5648. Epub 2017 May 18.
8
Cancerous inhibitor of protein phosphatase 2A, an emerging human oncoprotein and a potential cancer therapy target.癌性蛋白磷酸酶 2A 抑制剂,一种新兴的人类癌蛋白和潜在的癌症治疗靶点。
Cancer Res. 2013 Nov 15;73(22):6548-53. doi: 10.1158/0008-5472.CAN-13-1994. Epub 2013 Nov 7.
9
Ets1 and Elk1 transcription factors regulate cancerous inhibitor of protein phosphatase 2A expression in cervical and endometrial carcinoma cells.Ets1和Elk1转录因子调控子宫颈癌和子宫内膜癌细胞中蛋白磷酸酶2A的癌性抑制剂表达。
Transcription. 2012 Nov-Dec;3(6):323-35. doi: 10.4161/trns.22518. Epub 2012 Nov 1.
10
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.靶向乳腺癌中的 c-MYC 通过拮抗 PP2A 抑制剂。
Proc Natl Acad Sci U S A. 2014 Jun 24;111(25):9157-62. doi: 10.1073/pnas.1317630111. Epub 2014 Jun 9.

引用本文的文献

1
Emerging roles of the cancerous inhibitor of protein phosphatase 2A (CIP2A) in ovarian cancer.蛋白磷酸酶2A癌性抑制剂(CIP2A)在卵巢癌中的新作用。
Sci Rep. 2025 Jul 1;15(1):22382. doi: 10.1038/s41598-025-05013-0.
2
The mechanism of action and therapeutic potential of tumor-associated macrophages in tumor immune evasion.肿瘤相关巨噬细胞在肿瘤免疫逃逸中的作用机制及治疗潜力
Front Immunol. 2025 Apr 22;16:1545928. doi: 10.3389/fimmu.2025.1545928. eCollection 2025.
3
From Basic Science to Clinical Practice: The Role of Cancerous Inhibitor of Protein Phosphatase 2A (CIP2A)/p90 in Cancer.

本文引用的文献

1
Ethoxysanguinarine Induces Inhibitory Effects and Downregulates CIP2A in Lung Cancer Cells.乙氧基血根碱对肺癌细胞具有抑制作用并下调CIP2A表达。
ACS Med Chem Lett. 2013 Dec 20;5(2):113-8. doi: 10.1021/ml400341k. eCollection 2014 Feb 13.
2
Expression patterns of microRNA-218 and its potential functions by targeting CIP2A and BMI1 genes in melanoma.微小RNA-218在黑色素瘤中通过靶向CIP2A和BMI1基因的表达模式及其潜在功能
Tumour Biol. 2014 Aug;35(8):8007-15. doi: 10.1007/s13277-014-2079-6. Epub 2014 May 18.
3
Molecular pathways: harnessing E2F1 regulation for prosenescence therapy in p53-defective cancer cells.
从基础科学到临床实践:蛋白磷酸酶2A癌性抑制剂(CIP2A)/p90在癌症中的作用
Front Genet. 2023 Feb 24;14:1110656. doi: 10.3389/fgene.2023.1110656. eCollection 2023.
4
Cancerous inhibitor of protein phosphatase 2A enhances chemoresistance of gastric cancer cells to oxaliplatin.蛋白磷酸酶2A的癌性抑制剂增强胃癌细胞对奥沙利铂的化疗耐药性。
World J Gastrointest Oncol. 2023 Feb 15;15(2):286-302. doi: 10.4251/wjgo.v15.i2.286.
5
The Pivotal Role of Protein Phosphatase 2A (PP2A) in Brain Tumors.蛋白磷酸酶 2A(PP2A)在脑肿瘤中的关键作用。
Int J Mol Sci. 2022 Dec 11;23(24):15717. doi: 10.3390/ijms232415717.
6
Fusicoccin-A Targets Cancerous Inhibitor of Protein Phosphatase 2A by Stabilizing a C-Terminal Interaction with 14-3-3.福司可林 A 通过稳定与 14-3-3 的 C 端相互作用来靶向蛋白磷酸酶 2A 的致癌抑制剂。
ACS Chem Biol. 2022 Nov 18;17(11):2972-2978. doi: 10.1021/acschembio.2c00299. Epub 2022 Oct 18.
7
Oct4 facilitates chondrogenic differentiation of mesenchymal stem cells by mediating CIP2A expression.Oct4 通过介导 CIP2A 的表达促进间充质干细胞的软骨分化。
Cell Tissue Res. 2022 Jul;389(1):11-21. doi: 10.1007/s00441-022-03619-8. Epub 2022 Apr 18.
8
CIP2A as a Key Regulator for AKT Phosphorylation Has Partial Impact Determining Clinical Outcome in Breast Cancer.CIP2A作为AKT磷酸化的关键调节因子,在决定乳腺癌临床结果方面具有部分影响。
J Clin Med. 2022 Mar 14;11(6):1610. doi: 10.3390/jcm11061610.
9
MHC Phosphopeptides: Promising Targets for Immunotherapy of Cancer and Other Chronic Diseases.MHC 磷酸肽:癌症和其他慢性疾病免疫治疗的有前途的靶点。
Mol Cell Proteomics. 2021;20:100112. doi: 10.1016/j.mcpro.2021.100112. Epub 2021 Jun 12.
10
Association of the Epithelial-Mesenchymal Transition (EMT) with Cisplatin Resistance.上皮-间充质转化(EMT)与顺铂耐药的关系。
Int J Mol Sci. 2020 Jun 3;21(11):4002. doi: 10.3390/ijms21114002.
分子途径:利用 E2F1 调控治疗 p53 缺陷型癌细胞的衰老。
Clin Cancer Res. 2014 Jul 15;20(14):3644-50. doi: 10.1158/1078-0432.CCR-13-1942. Epub 2014 May 1.
4
Effect of FTY720 on the SET-PP2A complex in acute myeloid leukemia; SET binding drugs have antagonistic activity.FTY720对急性髓系白血病中SET-PP2A复合物的影响;SET结合药物具有拮抗活性。
Leukemia. 2014 Sep;28(9):1915-8. doi: 10.1038/leu.2014.141. Epub 2014 Apr 30.
5
miR-375 activates p21 and suppresses telomerase activity by coordinately regulating HPV E6/E7, E6AP, CIP2A, and 14-3-3ζ.微小RNA-375通过协同调节人乳头瘤病毒E6/E7、E6相关蛋白、癌抑制蛋白2A和14-3-3ζ激活p21并抑制端粒酶活性。
Mol Cancer. 2014 Apr 8;13:80. doi: 10.1186/1476-4598-13-80.
6
Targeting inhibitors of the tumor suppressor PP2A for the treatment of pancreatic cancer.靶向肿瘤抑制因子PP2A的抑制剂用于治疗胰腺癌。
Mol Cancer Res. 2014 Jun;12(6):924-39. doi: 10.1158/1541-7786.MCR-13-0542. Epub 2014 Mar 25.
7
A diverse array of cancer-associated MTOR mutations are hyperactivating and can predict rapamycin sensitivity.各种各样与癌症相关的MTOR突变具有超激活作用,并且能够预测雷帕霉素敏感性。
Cancer Discov. 2014 May;4(5):554-63. doi: 10.1158/2159-8290.CD-13-0929. Epub 2014 Mar 14.
8
CIP2A oncoprotein controls cell growth and autophagy through mTORC1 activation.CIP2A 癌蛋白通过激活 mTORC1 来控制细胞生长和自噬。
J Cell Biol. 2014 Mar 3;204(5):713-27. doi: 10.1083/jcb.201304012.
9
Doubling down on the PI3K-AKT-mTOR pathway enhances the antitumor efficacy of PARP inhibitor in triple negative breast cancer model beyond BRCA-ness.双重抑制 PI3K-AKT-mTOR 通路可增强 PARP 抑制剂在三阴性乳腺癌模型中的抗肿瘤疗效,超越 BRCA 状态。
Neoplasia. 2014 Jan;16(1):43-72. doi: 10.1593/neo.131694.
10
Opposing role of Notch1 and Notch2 in a Kras(G12D)-driven murine non-small cell lung cancer model.Notch1 和 Notch2 在 Kras(G12D)驱动的小鼠非小细胞肺癌模型中的拮抗作用。
Oncogene. 2015 Jan 29;34(5):578-88. doi: 10.1038/onc.2013.592. Epub 2014 Feb 10.