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1
Signaling of miRNAs-FOXM1 in cancer and potential targeted therapy.miRNAs-FOXM1 信号在癌症中的作用及潜在的靶向治疗。
Curr Drug Targets. 2013 Sep;14(10):1192-202. doi: 10.2174/13894501113149990192.
2
Targeting miRNAs for pancreatic cancer therapy.靶向微小RNA用于胰腺癌治疗
Curr Pharm Des. 2014;20(33):5279-86. doi: 10.2174/1381612820666140128210443.
3
MicroRNA-370 directly targets FOXM1 to inhibit cell growth and metastasis in osteosarcoma cells.微小RNA-370直接靶向叉头框蛋白M1以抑制骨肉瘤细胞的生长和转移。
Int J Clin Exp Pathol. 2015 Sep 1;8(9):10250-60. eCollection 2015.
4
Targeting FOXM1 in cancer.靶向癌症中的 FOXM1。
Biochem Pharmacol. 2013 Mar 1;85(5):644-652. doi: 10.1016/j.bcp.2012.10.013. Epub 2012 Oct 24.
5
FOXM1 and its oncogenic signaling in pancreatic cancer pathogenesis.FOXM1及其在胰腺癌发病机制中的致癌信号传导。
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FOXM1 (Forkhead box M1) in tumorigenesis: overexpression in human cancer, implication in tumorigenesis, oncogenic functions, tumor-suppressive properties, and target of anticancer therapy.FOXM1(叉头框蛋白 M1)在肿瘤发生中的作用:在人类癌症中的过表达、在肿瘤发生中的作用、致癌功能、肿瘤抑制特性以及抗癌治疗的靶点。
Adv Cancer Res. 2013;119:191-419. doi: 10.1016/B978-0-12-407190-2.00016-2.
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FOXM1: From cancer initiation to progression and treatment.叉头框蛋白M1:从癌症起始到进展及治疗
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MicroRNAs as the critical regulators of Forkhead box protein family during gynecological and breast tumor progression and metastasis.MicroRNAs 作为 Forkhead box 蛋白家族在妇科和乳腺肿瘤进展及转移中的关键调控因子。
Eur J Med Res. 2023 Sep 9;28(1):330. doi: 10.1186/s40001-023-01329-7.
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A lignan from Alnus japonica inhibits glioblastoma tumorspheres by suppression of FOXM1.日本桤木中的一种木脂素通过抑制 FOXM1 来抑制神经胶质瘤肿瘤球。
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FOXM1-induced miR-552 expression contributes to pancreatic cancer progression by targeting multiple tumor suppressor genes.FOXM1 诱导的 miR-552 表达通过靶向多个肿瘤抑制基因促进胰腺癌的进展。
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FOXM1 and Cancer: Faulty Cellular Signaling Derails Homeostasis.叉头框蛋白M1(FOXM1)与癌症:细胞信号传导异常破坏体内平衡。
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A cytoskeleton regulator AVIL drives tumorigenesis in glioblastoma.细胞骨架调节剂 AVIL 驱动脑胶质母细胞瘤的肿瘤发生。
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Lentiviral RNA interference-mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma .慢病毒RNA干扰介导的叉头框蛋白M1表达下调抑制口腔鳞状细胞癌生长
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Inhibition of Wnt3a/FOXM1/β-Catenin Axis and Activation of GSK3β and Caspases are Critically Involved in Apoptotic Effect of Moracin D in Breast Cancers.莫诺苷 D 通过抑制 Wnt3a/FOXM1/β-连环蛋白轴和激活 GSK3β 及半胱天冬酶诱导乳腺癌细胞凋亡。
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Downregulation of FoxM1 inhibits cell growth and migration and invasion in bladder cancer cells.FoxM1的下调抑制膀胱癌细胞的生长、迁移和侵袭。
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Sophoridine suppresses cell growth in human medulloblastoma through FoxM1, NF-κB and AP-1.槐定碱通过FoxM1、NF-κB和AP-1抑制人髓母细胞瘤细胞生长。
Oncol Lett. 2017 Dec;14(6):7941-7946. doi: 10.3892/ol.2017.7224. Epub 2017 Oct 19.

本文引用的文献

1
FoxM1 is overexpressed in Helicobacter pylori-induced gastric carcinogenesis and is negatively regulated by miR-370.FoxM1 在幽门螺杆菌诱导的胃癌发生中过表达,并受 miR-370 的负调控。
Mol Cancer Res. 2013 Aug;11(8):834-44. doi: 10.1158/1541-7786.MCR-13-0007. Epub 2013 Apr 10.
2
FOX(M1) news--it is cancer.福克斯新闻(M1)——这是癌症。
Mol Cancer Ther. 2013 Mar;12(3):245-54. doi: 10.1158/1535-7163.MCT-12-0712. Epub 2013 Feb 26.
3
Targeting FOXM1 in cancer.靶向癌症中的 FOXM1。
Biochem Pharmacol. 2013 Mar 1;85(5):644-652. doi: 10.1016/j.bcp.2012.10.013. Epub 2012 Oct 24.
4
miR-134 inhibits epithelial to mesenchymal transition by targeting FOXM1 in non-small cell lung cancer cells.miR-134 通过靶向 FOXM1 抑制非小细胞肺癌细胞的上皮间质转化。
FEBS Lett. 2012 Oct 19;586(20):3761-5. doi: 10.1016/j.febslet.2012.09.016. Epub 2012 Sep 23.
5
The tumor suppressive role of miRNA-370 by targeting FoxM1 in acute myeloid leukemia.miRNA-370 通过靶向 FoxM1 在急性髓系白血病中发挥肿瘤抑制作用。
Mol Cancer. 2012 Aug 17;11:56. doi: 10.1186/1476-4598-11-56.
6
A review on the role of microRNA in biology, diagnosis, and treatment of pancreatic adenocarcinoma.关于 microRNA 在胰腺腺癌的生物学、诊断和治疗中的作用的综述。
Pancreas. 2012 Jul;41(5):671-7. doi: 10.1097/MPA.0b013e31823c9d21.
7
Suppression of FOXM1 sensitizes human cancer cells to cell death induced by DNA-damage.抑制 FOXM1 可使人类癌细胞对 DNA 损伤诱导的细胞死亡敏感。
PLoS One. 2012;7(2):e31761. doi: 10.1371/journal.pone.0031761. Epub 2012 Feb 29.
8
The microcosmos of cancer.癌症的微观世界。
Nature. 2012 Feb 15;482(7385):347-55. doi: 10.1038/nature10888.
9
A novel FoxM1-caveolin signaling pathway promotes pancreatic cancer invasion and metastasis.一种新型的 FoxM1-小窝蛋白信号通路促进胰腺癌的侵袭和转移。
Cancer Res. 2012 Feb 1;72(3):655-65. doi: 10.1158/0008-5472.CAN-11-3102. Epub 2011 Dec 22.
10
Competitive interactions of cancer cells and normal cells via secretory microRNAs.癌细胞与正常细胞通过分泌 microRNAs 发生竞争相互作用。
J Biol Chem. 2012 Jan 6;287(2):1397-405. doi: 10.1074/jbc.M111.288662. Epub 2011 Nov 28.

miRNAs-FOXM1 信号在癌症中的作用及潜在的靶向治疗。

Signaling of miRNAs-FOXM1 in cancer and potential targeted therapy.

机构信息

Department of Surgery, Shanghai Jiaotong University Affiliated Ruijin Hospital, Shanghai, People’s Republic of China.

出版信息

Curr Drug Targets. 2013 Sep;14(10):1192-202. doi: 10.2174/13894501113149990192.

DOI:10.2174/13894501113149990192
PMID:23834153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4081534/
Abstract

The transcription factor Forkhead box protein M1 (FOXM1) is overexpressed in the majority of cancer patients. This overexpression is implicated to play a role in the pathogenesis, progression, and metastasis of cancer. This important role of FOXM1 demonstrates its significance to cancer therapy. MicroRNAs (miRNAs) are small noncoding, endogenous, single-stranded RNAs that are pivotal posttranscriptional gene expression regulators. MiRNAs aberrantly expressed in cancer cells have important roles in tumorigenesis and progression. Currently, miRNAs are being studied as diagnostic and prognostic biomarkers and therapeutic tools for cancer. The rapid discovery of many target miRNAs and their relevant pathways has contributed to the development of miRNA-based therapeutics for cancer. In this review, we summarize the latest and most significant findings on FOXM1 and miRNA involvement in cancer development and describe the role/roles of miRNA/FOXM1 signaling pathways in cancer initiation and progression. Targeting FOXM1 via regulation of miRNA expression may have a role in cancer treatment, although the miRNA delivery method remains the key challenge to the establishment of this novel therapy.

摘要

转录因子叉头框蛋白 M1(FOXM1)在大多数癌症患者中过度表达。这种过表达被认为在癌症的发病机制、进展和转移中起作用。FOXM1 的重要作用表明其对癌症治疗的重要性。微小 RNA(miRNA)是小的非编码、内源性、单链 RNA,是转录后基因表达调控的关键。在癌细胞中异常表达的 miRNA 在肿瘤发生和进展中具有重要作用。目前,miRNA 被作为癌症的诊断和预后生物标志物以及治疗工具进行研究。许多靶 miRNA 及其相关途径的快速发现促进了 miRNA 为基础的癌症治疗方法的发展。在这篇综述中,我们总结了关于 FOXM1 和 miRNA 参与癌症发生和发展的最新和最重要的发现,并描述了 miRNA/FOXM1 信号通路在癌症起始和进展中的作用。通过调节 miRNA 表达靶向 FOXM1 可能在癌症治疗中发挥作用,尽管 miRNA 递送方法仍然是建立这种新疗法的关键挑战。