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miRNAs 在黑色素瘤及其对治疗的抵抗中的作用。

The miRNAs Role in Melanoma and in Its Resistance to Therapy.

机构信息

IRBM S.p.A., Via Pontina Km 30,600, I-00071 Pomezia, Italy.

Institute of Genetics and Biophysics -I.G.B., Adriano Buzzati-Traverso, Consiglio Nazionale delle Ricerche (CNR), Via Pietro Castellino, 111, I-80131 Naples, Italy.

出版信息

Int J Mol Sci. 2020 Jan 29;21(3):878. doi: 10.3390/ijms21030878.

DOI:10.3390/ijms21030878
PMID:32013263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7037367/
Abstract

Melanoma is the less common but the most malignant skin cancer. Since the survival rate of melanoma metastasis is about 10-15%, many different studies have been carried out in order to find a more effective treatment. Although the development of target-based therapies and immunotherapeutic strategies has improved chances for patient survival, melanoma treatment still remains a big challenge for oncologists. Here, we collect recent data about the emerging role of melanoma-associated microRNAs (miRNAs) currently available treatments, and their involvement in drug resistance. We also reviewed miRNAs as prognostic factors, because of their chemical stability and resistance to RNase activity, in melanoma progression. Moreover, despite miRNAs being considered small conserved regulators with the limitation of target specificity, we outline the dual role of melanoma-associated miRNAs, as oncogenic and/or tumor suppressive factors, compared to other tumors.

摘要

黑色素瘤是一种不太常见但恶性程度最高的皮肤癌。由于黑色素瘤转移的存活率约为 10-15%,因此进行了许多不同的研究,以寻找更有效的治疗方法。尽管基于靶点的治疗方法和免疫治疗策略的发展提高了患者的生存机会,但黑色素瘤的治疗仍然是肿瘤学家面临的一个巨大挑战。在这里,我们收集了有关黑色素瘤相关 microRNAs (miRNAs) 目前可用治疗方法的最新数据及其在耐药性中的作用。我们还回顾了 miRNAs 作为预后因素,因为它们具有化学稳定性和对核糖核酸酶活性的抗性,在黑色素瘤的进展中。此外,尽管 miRNAs 被认为是具有靶向特异性限制的小保守调节因子,但我们概述了与其他肿瘤相比,黑色素瘤相关 miRNAs 作为致癌和/或肿瘤抑制因子的双重作用。

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本文引用的文献

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Leveraging transcriptional dynamics to improve BRAF inhibitor responses in melanoma.利用转录动态变化提高黑色素瘤对 BRAF 抑制剂的反应。
EBioMedicine. 2019 Oct;48:178-190. doi: 10.1016/j.ebiom.2019.09.023. Epub 2019 Oct 5.
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MicroRNA Ratios Distinguish Melanomas from Nevi.miRNA 比值可区分黑素瘤与痣。
J Invest Dermatol. 2020 Jan;140(1):164-173.e7. doi: 10.1016/j.jid.2019.06.126. Epub 2019 Sep 30.
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Sensitive Detection and Analysis of Neoantigen-Specific T Cell Populations from Tumors and Blood.从肿瘤和血液中检测和分析新抗原特异性 T 细胞群体
miRNA亚型在黑色素瘤中的预后意义:一项生存分析及与各患者阶段治疗反应的相关性
Biomedicines. 2024 Dec 11;12(12):2809. doi: 10.3390/biomedicines12122809.
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Evaluation of the Anti-Cancer Potential of Extracellular Vesicles Derived from Human Amniotic Fluid Stem Cells: Focus on Effective miRNAs in the Treatment of Melanoma Progression.评估人羊水干细胞来源的细胞外囊泡的抗癌潜力:聚焦于治疗黑色素瘤进展中的有效微小RNA
Int J Mol Sci. 2024 Nov 21;25(23):12502. doi: 10.3390/ijms252312502.
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Melanoma Metabolism: Molecular Mechanisms and Therapeutic Implications in Cutaneous Oncology.黑色素瘤代谢:皮肤肿瘤学中的分子机制与治疗意义。
Cancer Med. 2024 Nov;13(21):e70386. doi: 10.1002/cam4.70386.
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miR-876-3p is a tumor suppressor on 9p21 that is inactivated in melanoma and targets ERK.miR-876-3p 是位于 9p21 上的肿瘤抑制因子,在黑色素瘤中失活,靶向 ERK。
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Transcriptome-Wide Association Study Reveals New Molecular Interactions Associated with Melanoma Pathogenesis.全转录组关联研究揭示与黑色素瘤发病机制相关的新分子相互作用。
Cancers (Basel). 2024 Jul 11;16(14):2517. doi: 10.3390/cancers16142517.
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Front Oncol. 2024 May 17;14:1385632. doi: 10.3389/fonc.2024.1385632. eCollection 2024.
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Curr Oncol. 2024 May 17;31(5):2881-2894. doi: 10.3390/curroncol31050220.
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Cell Rep. 2019 Sep 3;28(10):2728-2738.e7. doi: 10.1016/j.celrep.2019.07.106.
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