• 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

携带微小RNA-143的三重调控溶瘤腺病毒在结直肠癌中显示出强大的抗肿瘤功效。

A Triple-Regulated Oncolytic Adenovirus Carrying MicroRNA-143 Exhibits Potent Antitumor Efficacy in Colorectal Cancer.

作者信息

Luo Qifeng, Song Hongming, Deng Xiaochong, Li Jiayi, Jian Wei, Zhao Junyong, Zheng Xueyu, Basnet Shiva, Ge Haiyan, Daniel Twingle, Xu Bin, Fang Lin

机构信息

Department of General Surgery, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, P. R. China.

Breast Disease Center, The Affiliated Hospital of Qingdao University, Shandong 266000, P. R. China.

出版信息

Mol Ther Oncolytics. 2020 Jan 25;16:219-229. doi: 10.1016/j.omto.2020.01.005. eCollection 2020 Mar 27.

DOI:10.1016/j.omto.2020.01.005
PMID:32123722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7036723/
Abstract

The cancer-targeting gene virotherapy might be a useful strategy for the treatment of cancer, because it could combine the advantages of both gene therapy and virotherapy. This study aimed to construct a triple-regulated oncolytic adenovirus, Ad-RGD-Survivin-ZD55-miR-143, carrying the therapeutic gene miR-143 and evaluate its possible antitumor effect in colorectal cancer. We observed that miR-143 was lowly expressed in patients with colorectal cancer. The upregulation of miR-143 could inhibit cell proliferation and induce cell apoptosis by targeting KRAS in colorectal cancer cells. Then, Ad-RGD-Survivin-ZD55-miR-143 was successfully constructed in this study. Cells infected with Ad-RGD-Survivin-ZD55-miR-143 could inhibit cell proliferation, suppress cell migration and invasion, arrest cells at the G1 phase, and induce cellular apoptosis. At the same time, Ad-RGD-Survivin-ZD55-miR-143 decreased the expression of PARP-1 and KRAS protein . In a HCT116 xenograft model, intratumoral injection of Ad-RGD-Survivin-ZD55-miR-143 resulted in reduced tumor growth. Furthermore, Ad-RGD-Survivin-ZD55-miR-143 induced apoptosis and decreased the expression level of KRAS in HCT116 xenograft cells. Our results suggested that Ad-RGD-Survivin-ZD55-miR-143 produced a strong antitumor effect by targeting KRAS and that this strategy could broaden the therapeutic options for treating colorectal cancer.

摘要

癌症靶向基因病毒疗法可能是一种治疗癌症的有效策略,因为它可以结合基因疗法和病毒疗法的优点。本研究旨在构建一种携带治疗性基因miR-143的三重调控溶瘤腺病毒Ad-RGD-Survivin-ZD55-miR-143,并评估其在结直肠癌中的可能抗肿瘤作用。我们观察到miR-143在结直肠癌患者中低表达。miR-143的上调可通过靶向结直肠癌细胞中的KRAS来抑制细胞增殖并诱导细胞凋亡。然后,本研究成功构建了Ad-RGD-Survivin-ZD55-miR-143。感染Ad-RGD-Survivin-ZD55-miR-143的细胞可抑制细胞增殖、抑制细胞迁移和侵袭、使细胞停滞在G1期并诱导细胞凋亡。同时,Ad-RGD-Survivin-ZD55-miR-143降低了PARP-1和KRAS蛋白的表达。在HCT116异种移植模型中,瘤内注射Ad-RGD-Survivin-ZD55-miR-143导致肿瘤生长减缓。此外,Ad-RGD-Survivin-ZD55-miR-143诱导HCT116异种移植细胞凋亡并降低KRAS的表达水平。我们的结果表明,Ad-RGD-Survivin-ZD55-miR-143通过靶向KRAS产生了强大的抗肿瘤作用,并且该策略可以拓宽结直肠癌的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/cc75bf61ea42/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/38f8e45a2727/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/b55b70ebf5b0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/7a46c95da9f8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/c35854be0e76/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/cc75bf61ea42/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/38f8e45a2727/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/b55b70ebf5b0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/7a46c95da9f8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/c35854be0e76/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/7036723/cc75bf61ea42/gr5.jpg

相似文献

1
A Triple-Regulated Oncolytic Adenovirus Carrying MicroRNA-143 Exhibits Potent Antitumor Efficacy in Colorectal Cancer.携带微小RNA-143的三重调控溶瘤腺病毒在结直肠癌中显示出强大的抗肿瘤功效。
Mol Ther Oncolytics. 2020 Jan 25;16:219-229. doi: 10.1016/j.omto.2020.01.005. eCollection 2020 Mar 27.
2
A dual-regulated oncolytic adenovirus carrying TAp63 gene exerts potent antitumor effect on colorectal cancer cells.携带TAp63基因的双调控溶瘤腺病毒对结肠癌细胞具有强大的抗肿瘤作用。
Am J Transl Res. 2017 Jun 15;9(6):2966-2974. eCollection 2017.
3
A novel E1B55kDa-deleted oncolytic adenovirus carrying microRNA-143 exerts specific antitumor efficacy on colorectal cancer cells.一种携带微小RNA - 143的新型E1B55kDa缺失型溶瘤腺病毒对结肠癌细胞具有特异性抗肿瘤作用。
Am J Transl Res. 2016 Sep 15;8(9):3822-3830. eCollection 2016.
4
Potent antitumor efficacy of ST13 for colorectal cancer mediated by oncolytic adenovirus via mitochondrial apoptotic cell death.溶瘤腺病毒介导的ST13通过线粒体凋亡性细胞死亡对结直肠癌具有强大的抗肿瘤功效。
Hum Gene Ther. 2008 Apr;19(4):343-53. doi: 10.1089/hum.2007.0137.
5
Oncolytic adenovirus mediated Survivin knockdown by RNA interference suppresses human colorectal carcinoma growth in vitro and in vivo.溶瘤腺病毒介导的RNA干扰沉默Survivin基因可抑制人结直肠癌的体内外生长。
J Exp Clin Cancer Res. 2009 Jun 15;28(1):81. doi: 10.1186/1756-9966-28-81.
6
Potent antitumor activity of oncolytic adenovirus expressing mda-7/IL-24 for colorectal cancer.表达mda-7/IL-24的溶瘤腺病毒对结直肠癌具有强大的抗肿瘤活性。
Hum Gene Ther. 2005 Jul;16(7):845-58. doi: 10.1089/hum.2005.16.845.
7
The antitumor activity of TRAIL and IL-24 with replicating oncolytic adenovirus in colorectal cancer.TRAIL与IL-24联合复制型溶瘤腺病毒在结直肠癌中的抗肿瘤活性。
Cancer Gene Ther. 2006 Nov;13(11):1011-22. doi: 10.1038/sj.cgt.7700969. Epub 2006 Jun 23.
8
Combination of ZD55-MnSOD therapy with 5-FU enhances antitumor efficacy in colorectal cancer.ZD55-MnSOD疗法与5-氟尿嘧啶联合使用可增强结直肠癌的抗肿瘤疗效。
J Cancer Res Clin Oncol. 2008 Feb;134(2):219-26. doi: 10.1007/s00432-007-0273-2. Epub 2007 Jul 14.
9
Oncolytic virus carrying shRNA targeting SATB1 inhibits prostate cancer growth and metastasis.携带靶向SATB1的短发夹RNA的溶瘤病毒可抑制前列腺癌的生长和转移。
Tumour Biol. 2015 Nov;36(11):9073-81. doi: 10.1007/s13277-015-3658-x. Epub 2015 Jun 19.
10
Complete elimination of colorectal tumor xenograft by combined manganese superoxide dismutase with tumor necrosis factor-related apoptosis-inducing ligand gene virotherapy.通过联合锰超氧化物歧化酶与肿瘤坏死因子相关凋亡诱导配体基因病毒疗法完全消除结直肠癌异种移植瘤
Cancer Res. 2006 Apr 15;66(8):4291-8. doi: 10.1158/0008-5472.CAN-05-1834.

引用本文的文献

1
Precision oncolytic viral therapy in colorectal cancer: Genetic targeting and immune modulation for personalized treatment (Review).结直肠癌的精准溶瘤病毒疗法:用于个性化治疗的基因靶向和免疫调节(综述)
Int J Mol Med. 2025 Jul;56(1). doi: 10.3892/ijmm.2025.5545. Epub 2025 May 9.
2
The long-term effectiveness and mechanism of oncolytic virotherapy combined with anti-PD-L1 antibody in colorectal cancer patient.溶瘤病毒疗法联合抗PD-L1抗体治疗结直肠癌患者的长期疗效及机制
Cancer Gene Ther. 2024 Sep;31(9):1412-1426. doi: 10.1038/s41417-024-00807-2. Epub 2024 Jul 27.
3
The investigation of oncolytic viruses in the field of cancer therapy.

本文引用的文献

1
Heterologous Immunity between Adenoviruses and Hepatitis C Virus (HCV): Recombinant Adenovirus Vaccine Vectors Containing Antigens from Unrelated Pathogens Induce Cross-Reactive Immunity Against HCV Antigens.腺病毒与丙型肝炎病毒(HCV)之间的异源免疫:含有来自无关病原体抗原的重组腺病毒疫苗载体诱导针对 HCV 抗原的交叉反应性免疫。
Cells. 2019 May 26;8(5):507. doi: 10.3390/cells8050507.
2
MicroRNA-143-3p inhibits colorectal cancer metastases by targeting ITGA6 and ASAP3.microRNA-143-3p 通过靶向 ITGA6 和 ASAP3 抑制结直肠癌细胞转移。
Cancer Sci. 2019 Feb;110(2):805-816. doi: 10.1111/cas.13910. Epub 2019 Jan 4.
3
The Current Status and Future Prospects of Oncolytic Viruses in Clinical Trials against Melanoma, Glioma, Pancreatic, and Breast Cancers.
溶瘤病毒在癌症治疗领域的研究。
Front Oncol. 2024 Jul 10;14:1423143. doi: 10.3389/fonc.2024.1423143. eCollection 2024.
4
Optimal delivery of RNA interference by viral vectors for cancer therapy.病毒载体介导的 RNA 干扰在癌症治疗中的最佳传递。
Mol Ther. 2023 Nov 1;31(11):3127-3145. doi: 10.1016/j.ymthe.2023.09.012. Epub 2023 Sep 20.
5
Application of Peptides in Construction of Nonviral Vectors for Gene Delivery.肽在构建用于基因递送的非病毒载体中的应用。
Nanomaterials (Basel). 2022 Nov 19;12(22):4076. doi: 10.3390/nano12224076.
6
Immunovirotherapy: The role of antibody based therapeutics combination with oncolytic viruses.免疫病毒疗法:抗体药物与溶瘤病毒联合治疗的作用。
Front Immunol. 2022 Oct 13;13:1012806. doi: 10.3389/fimmu.2022.1012806. eCollection 2022.
7
MicroRNAs Are Key Molecules Involved in the Gene Regulation Network of Colorectal Cancer.微小RNA是参与结直肠癌基因调控网络的关键分子。
Front Cell Dev Biol. 2022 Apr 8;10:828128. doi: 10.3389/fcell.2022.828128. eCollection 2022.
8
Engineering strategies to enhance oncolytic viruses in cancer immunotherapy.工程策略增强溶瘤病毒在癌症免疫治疗中的作用。
Signal Transduct Target Ther. 2022 Apr 6;7(1):117. doi: 10.1038/s41392-022-00951-x.
9
Combination of oncolytic adenovirus ZD55 harboring TRAIL-IETD-MnSOD and cytokine-induced killer cells against lung cancer.携带TRAIL-IETD-MnSOD的溶瘤腺病毒ZD55与细胞因子诱导的杀伤细胞联合治疗肺癌。
Ann Transl Med. 2021 Oct;9(20):1527. doi: 10.21037/atm-21-4479.
10
MiR-9-1 Suppresses Cell Proliferation and Promotes Apoptosis by Targeting UHRF1 in Lung Cancer.miR-9-1 通过靶向 UHRF1 抑制肺癌细胞增殖并促进细胞凋亡。
Technol Cancer Res Treat. 2021 Jan-Dec;20:15330338211041191. doi: 10.1177/15330338211041191.
溶瘤病毒在针对黑色素瘤、神经胶质瘤、胰腺癌和乳腺癌的临床试验中的现状与未来前景
Cancers (Basel). 2018 Sep 26;10(10):356. doi: 10.3390/cancers10100356.
4
Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.全球癌症统计数据 2018:GLOBOCAN 对全球 185 个国家/地区 36 种癌症的发病率和死亡率的估计。
CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
5
The Impact of Primary Tumor Location on Long-Term Survival in Patients Undergoing Hepatic Resection for Metastatic Colon Cancer.原发肿瘤位置对转移性结肠癌患者肝切除术后长期生存的影响。
Ann Surg Oncol. 2018 Feb;25(2):431-438. doi: 10.1245/s10434-017-6264-x. Epub 2017 Nov 27.
6
Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer.鉴定一种十六种微小RNA特征作为II期和III期结肠癌的预后生物标志物。
Oncotarget. 2017 Sep 23;8(50):87837-87847. doi: 10.18632/oncotarget.21237. eCollection 2017 Oct 20.
7
miR-143 and miR-145 inhibit gastric cancer cell migration and metastasis by suppressing MYO6.miR-143 和 miR-145 通过抑制 MYO6 抑制胃癌细胞迁移和转移。
Cell Death Dis. 2017 Oct 12;8(10):e3101. doi: 10.1038/cddis.2017.493.
8
Oncolytic viral therapy for pancreatic cancer.胰腺癌的溶瘤病毒疗法。
J Surg Oncol. 2017 Jul;116(1):94-103. doi: 10.1002/jso.24626. Epub 2017 Apr 13.
9
Current status of clinical trials assessing oncolytic virus therapy for urological cancers.评估溶瘤病毒疗法用于泌尿系统癌症的临床试验现状
Int J Urol. 2017 May;24(5):342-351. doi: 10.1111/iju.13325. Epub 2017 Mar 21.
10
Oncolytic Virotherapy for the Treatment of Malignant Glioma.溶瘤病毒疗法治疗恶性胶质瘤
Neurotherapeutics. 2017 Apr;14(2):333-344. doi: 10.1007/s13311-017-0516-0.