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Dicer的抑制与卵巢癌的侵袭性表型和化疗耐药性相关。

Repression of Dicer is associated with invasive phenotype and chemoresistance in ovarian cancer.

作者信息

Kuang Yan, Cai Jing, Li Donglin, Han Qin, Cao Jin, Wang Zehua

机构信息

Department of Obstetrics and Gynecology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022; ; Department of Obstetrics and Gynecology, First Affiliated Hospital, GuangXi Medical University, Nanning 530021, P.R. China.

出版信息

Oncol Lett. 2013 Apr;5(4):1149-1154. doi: 10.3892/ol.2013.1158. Epub 2013 Jan 28.

DOI:10.3892/ol.2013.1158
PMID:23599754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3629258/
Abstract

Dicer is a key enzyme that processes microRNA (miRNA) precursors into their mature form, enabling them to regulate gene expression. However, the effects of Dicer on the biological behavior of cancer cells remain largely unclear. In this study, it was demonstrated that Dicer down-regulation promoted cell proliferation, migration and cell cycle progression in A2780 and SKOV3 ovarian cancer cells. Furthermore, Dicer expression was significantly decreased in cisplatin-resistant A2780 cells (A2780/DDP) compared with parental A2780 cells. Knockdown of Dicer by RNA interference decreased the sensitivity of A2780 cells to cisplatin. Moreover, EZH2 depletion by short hairpin RNA (shRNA) increased the expression of Dicer . Our data suggest that Dicer is involved in numerous biological/pathological processes, including drug resistance in ovarian cancer, and that its expression may be regulated by EZH2.

摘要

Dicer是一种关键酶,可将微小RNA(miRNA)前体加工成成熟形式,使其能够调节基因表达。然而,Dicer对癌细胞生物学行为的影响仍 largely不清楚。在本研究中,证明了Dicer下调促进了A2780和SKOV3卵巢癌细胞的增殖、迁移和细胞周期进程。此外,与亲本A2780细胞相比,顺铂耐药的A2780细胞(A2780/DDP)中Dicer表达显著降低。通过RNA干扰敲低Dicer降低了A2780细胞对顺铂的敏感性。此外,短发夹RNA(shRNA)介导的EZH2缺失增加了Dicer的表达。我们的数据表明,Dicer参与了包括卵巢癌耐药性在内的众多生物学/病理过程,并且其表达可能受EZH2调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/843e82f1b0fe/OL-05-04-1149-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/73c78fdd5810/OL-05-04-1149-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/c081e4f8dc96/OL-05-04-1149-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/81dd4d0d96a6/OL-05-04-1149-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/843e82f1b0fe/OL-05-04-1149-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/73c78fdd5810/OL-05-04-1149-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/c081e4f8dc96/OL-05-04-1149-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/81dd4d0d96a6/OL-05-04-1149-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce7/3629258/843e82f1b0fe/OL-05-04-1149-g03.jpg

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Silencing of Kruppel-like factor 2 by the histone methyltransferase EZH2 in human cancer.EZH2 通过组蛋白甲基转移酶沉默人癌症中的 Kruppel 样因子 2。
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Impaired MicroRNA Processing Facilitates Breast Cancer Cell Invasion by Upregulating Urokinase-Type Plasminogen Activator Expression.
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Cell Oncol (Dordr). 2024 Apr;47(2):677-693. doi: 10.1007/s13402-023-00892-9. Epub 2023 Nov 9.
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EZH2 Inhibition and Cisplatin as a Combination Anticancer Therapy: An Overview of Preclinical Studies.EZH2抑制与顺铂联合作为抗癌疗法:临床前研究综述
Cancers (Basel). 2022 Sep 29;14(19):4761. doi: 10.3390/cancers14194761.
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Dicer-mediated miR-200b expression contributes to cell migratory/invasive abilities and cancer stem cells properties of breast cancer cells.Dicer介导的miR-200b表达有助于乳腺癌细胞的细胞迁移/侵袭能力和癌症干细胞特性。
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