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微小RNA在胰腺癌进展中的作用

The Roles of MicroRNA in Pancreatic Cancer Progression.

作者信息

Kt Ramya Devi, Karthick Dharshene, Saravanaraj Kirtikesav Salem, Jaganathan M K, Ghorai Suvankar, Hemdev Sanjana Prakash

机构信息

Department of Biotechnology, School of Bioengineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Tamil Nadu, India.

Department of Microbiology, Raiganj University, Uttar Dinajpur, India.

出版信息

Cancer Invest. 2022 Sep;40(8):700-709. doi: 10.1080/07357907.2022.2057526. Epub 2022 May 12.

DOI:10.1080/07357907.2022.2057526
PMID:35333689
Abstract

Pancreatic Ductal Adenocarcinoma (PDAC) has a poor patient survival rate in comparison with other cancer types, even after targeted therapy, chemotherapy, and immunotherapy. Therefore, a great deal needs to be done to gain a better understanding of the biology and identification of prognostic and predictive markers for the development of superior therapies. The microRNAs (miRNAs) belong to small non-coding RNAs that regulate post-transcriptional gene expression. Several shreds of evidence indicate that miRNAs play an important role in the pathogenesis of pancreatic cancer. Here we review the recent developments in miRNAs and their target role in the development, metastasis, migration, and invasion.

摘要

与其他癌症类型相比,胰腺导管腺癌(PDAC)患者的生存率较低,即使在接受靶向治疗、化疗和免疫治疗后也是如此。因此,需要做大量工作来更好地了解其生物学特性,并确定用于开发更优疗法的预后和预测标志物。微小RNA(miRNA)属于调控转录后基因表达的小型非编码RNA。有多项证据表明,miRNA在胰腺癌的发病机制中起重要作用。在此,我们综述了miRNA的最新研究进展及其在胰腺癌发生、转移、迁移和侵袭中的靶向作用。

相似文献

1
The Roles of MicroRNA in Pancreatic Cancer Progression.微小RNA在胰腺癌进展中的作用
Cancer Invest. 2022 Sep;40(8):700-709. doi: 10.1080/07357907.2022.2057526. Epub 2022 May 12.
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miRNA and Gene Expression in Pancreatic Ductal Adenocarcinoma.miRNA 和胰腺导管腺癌中的基因表达。
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Identification of candidate miRNA biomarkers for pancreatic ductal adenocarcinoma by weighted gene co-expression network analysis.通过加权基因共表达网络分析鉴定胰腺导管腺癌的候选 miRNA 生物标志物
Cell Oncol (Dordr). 2017 Apr;40(2):181-192. doi: 10.1007/s13402-017-0315-y. Epub 2017 Feb 15.
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MicroRNA in pancreatic adenocarcinoma: predictive/prognostic biomarkers or therapeutic targets?胰腺癌中的微小RNA:预测/预后生物标志物还是治疗靶点?
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Analysis of Blood Plasma MicroRNAs to Enable Identification of Patients with Pancreatic Ductal Adenocarcinoma Who Will Benefit from Surgical Resection.分析血浆微小RNA以鉴别能从手术切除中获益的胰腺导管腺癌患者。
Klin Onkol. 2019 Spring;32(Suppl 1):174-176.
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MiR-10b inhibits migration and invasion of pancreatic ductal adenocarcinoma via regulating E2F7.miR-10b 通过调控 E2F7 抑制胰腺导管腺癌的迁移和侵袭
J Clin Lab Anal. 2020 Oct;34(10):e23442. doi: 10.1002/jcla.23442. Epub 2020 Jun 26.
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Acta Biochim Pol. 2022 Jun 8;69(2):327-333. doi: 10.18388/abp.2020_5758.
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MicroRNA-891b is an independent prognostic factor of pancreatic cancer by targeting Cbl-b to suppress the growth of pancreatic cancer cells.微小RNA-891b通过靶向Cbl-b抑制胰腺癌细胞生长,是胰腺癌的独立预后因素。
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Clinical value of circular RNAs and autophagy-related miRNAs in the diagnosis and treatment of pancreatic cancer.环状 RNAs 和自噬相关 miRNAs 在胰腺癌诊断和治疗中的临床价值。
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引用本文的文献

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Analysis of Candidate miRNAs' Expression in Pancreatic Cancer.胰腺癌候选 miRNA 表达分析。
Cancer Med. 2024 Nov;13(21):e70400. doi: 10.1002/cam4.70400.
2
[Tumor-associated fibroblasts promotes proliferation and migration of prostate cancer cells by suppressing FBXL3 upregulating hsa-miR-18b-5p].肿瘤相关成纤维细胞通过抑制FBXL3上调hsa-miR-18b-5p促进前列腺癌细胞的增殖和迁移。
Nan Fang Yi Ke Da Xue Xue Bao. 2024 Jul 20;44(7):1284-1296. doi: 10.12122/j.issn.1673-4254.2024.07.08.
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MicroRNAs in Pancreatic Cancer: Advances in Biomarker Discovery and Therapeutic Implications.
胰腺癌细胞中的 microRNAs:生物标志物发现的新进展及其治疗意义。
Int J Mol Sci. 2024 Mar 31;25(7):3914. doi: 10.3390/ijms25073914.
4
Clinical value of the expression levels of tumor protein D52 and miR-133a on prognosis assessment of pancreatic cancer surgery.肿瘤蛋白D52和miR-133a表达水平对胰腺癌手术预后评估的临床价值
Pak J Med Sci. 2024 Mar-Apr;40(4):723-729. doi: 10.12669/pjms.40.4.8389.
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Identification and validation of the microRNAs and hub genes for pancreatic ductal adenocarcinoma by an integrated bioinformatic analysis.通过综合生物信息学分析鉴定和验证胰腺导管腺癌的微小RNA和枢纽基因
J Gastrointest Oncol. 2023 Apr 29;14(2):719-732. doi: 10.21037/jgo-23-192.