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本文引用的文献

1
Deregulated miRNAs in bone health: Epigenetic roles in osteoporosis.骨健康中失调的 miRNAs:骨质疏松症中的表观遗传作用。
Bone. 2019 May;122:52-75. doi: 10.1016/j.bone.2019.02.013. Epub 2019 Feb 14.
2
Increased serum levels of miR-214 in patients with PCa with bone metastasis may serve as a potential biomarker by targeting PTEN.前列腺癌骨转移患者血清中miR-214水平升高可能通过靶向PTEN作为一种潜在的生物标志物。
Oncol Lett. 2019 Jan;17(1):398-405. doi: 10.3892/ol.2018.9522. Epub 2018 Sep 28.
3
Promoter hypomethylation mediated upregulation of MicroRNA-10b-3p targets FOXO3 to promote the progression of esophageal squamous cell carcinoma (ESCC).启动子低甲基化介导 MicroRNA-10b-3p 的上调,靶向 FOXO3 促进食管鳞状细胞癌(ESCC)的进展。
J Exp Clin Cancer Res. 2018 Dec 4;37(1):301. doi: 10.1186/s13046-018-0966-1.
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miRNA-seq analysis of human vertebrae provides insight into the mechanism underlying GIOP.对人类椎骨的 miRNA-seq 分析为 GIOP 的发病机制提供了新的见解。
Bone. 2019 Mar;120:371-386. doi: 10.1016/j.bone.2018.11.013. Epub 2018 Nov 29.
5
Five microRNAs in serum as potential biomarkers for prostate cancer risk assessment and therapeutic intervention.血清中的五种微小RNA作为前列腺癌风险评估和治疗干预的潜在生物标志物。
Int Urol Nephrol. 2018 Dec;50(12):2193-2200. doi: 10.1007/s11255-018-2009-4. Epub 2018 Oct 15.
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miR-219a-5p Regulates Rorβ During Osteoblast Differentiation and in Age-related Bone Loss.miR-219a-5p 在成骨细胞分化和与年龄相关的骨丢失中调节 Rorβ。
J Bone Miner Res. 2019 Jan;34(1):135-144. doi: 10.1002/jbmr.3586. Epub 2018 Oct 15.
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Osteoblastic Factors in Prostate Cancer Bone Metastasis.成骨细胞因子在前列腺癌骨转移中的作用。
Curr Osteoporos Rep. 2018 Dec;16(6):642-647. doi: 10.1007/s11914-018-0480-6.
8
Serum miRNAs miR-140-3p and miR-23b-3p as potential biomarkers for osteoporosis and osteoporotic fracture in postmenopausal Mexican-Mestizo women.血清 microRNA miR-140-3p 和 miR-23b-3p 作为绝经后墨西哥裔妇女骨质疏松症和骨质疏松性骨折的潜在生物标志物。
Gene. 2018 Dec 30;679:19-27. doi: 10.1016/j.gene.2018.08.074. Epub 2018 Aug 30.
9
Expression of miR-30c and miR-29b in prostate cancer and its diagnostic significance.miR-30c和miR-29b在前列腺癌中的表达及其诊断意义。
Oncol Lett. 2018 Sep;16(3):3140-3144. doi: 10.3892/ol.2018.9007. Epub 2018 Jun 21.
10
miRNA-30 Family Members Inhibit Breast Cancer Invasion, Osteomimicry, and Bone Destruction by Directly Targeting Multiple Bone Metastasis-Associated Genes.miRNA-30 家族成员通过直接靶向多个骨转移相关基因抑制乳腺癌的侵袭、成骨样表型和骨质破坏。
Cancer Res. 2018 Sep 15;78(18):5259-5273. doi: 10.1158/0008-5472.CAN-17-3058. Epub 2018 Jul 24.

骨质疏松症中失调的 miRNA:在骨转移中的作用。

Deregulated miRNAs in osteoporosis: effects in bone metastasis.

机构信息

IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

Laboratory of Preclinical and Surgical Studies, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

出版信息

Cell Mol Life Sci. 2019 Oct;76(19):3723-3744. doi: 10.1007/s00018-019-03162-w. Epub 2019 May 30.

DOI:10.1007/s00018-019-03162-w
PMID:31147752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11105262/
Abstract

Starting from their role exerted on osteoblast and osteoclast differentiation and activity pathways, microRNAs (miRNAs) have been recently identified as regulators of different processes in bone homeostasis. For this purpose, in a recent review, we highlighted, as deregulated miRNAs could be involved in different bone diseases such as osteoporosis. In addition, recent studies supported the concept that osteoporosis-induced bone alterations might offer a receptive site for cancer cells to form bone metastases, However, to date, no data on specific-shared miRNAs between osteoporosis and bone metastases have been considered and described to clarify the evidence of this link. The main goal of this review is to underline as deregulated miRNAs in osteoporosis may have specific roles in the development of bone metastases. The review showed that several circulating osteoporotic miRNAs could facilitate tumor progression and bone-metastasis formation in several tumor types, i.e., breast cancer, prostate cancer, non-small-cell lung cancer, esophageal squamous cell carcinoma, and multiple myeloma. In detail, serum up-regulation of pro-osteoporotic miRNAs, as well as serum down-regulation of anti-osteoporotic miRNAs are common features of all these tumors and are able to promote bone metastasis. These results are of key importance and could help researcher and clinicians to establish new therapeutic strategies connected with deregulation of circulating miRNAs and able to interfere with pathogenic processes of osteoporosis, tumor progressions, and bone-metastasis formation.

摘要

从它们在成骨细胞和破骨细胞分化和活性途径中发挥的作用来看,微小 RNA(miRNA)最近被确定为骨稳态中不同过程的调节剂。为此,在最近的一篇综述中,我们强调了失调的 miRNA 可能参与了不同的骨骼疾病,如骨质疏松症。此外,最近的研究支持了这样一种观点,即骨质疏松症引起的骨骼改变可能为癌细胞形成骨转移提供了一个接受部位。然而,迄今为止,尚未考虑和描述骨质疏松症和骨转移之间特定共享 miRNA 的具体数据,以阐明这一联系的证据。本综述的主要目的是强调骨质疏松症中失调的 miRNA 可能在骨转移的发展中具有特定作用。该综述表明,几种循环骨质疏松症 miRNA 可能促进多种肿瘤类型(如乳腺癌、前列腺癌、非小细胞肺癌、食管鳞状细胞癌和多发性骨髓瘤)的肿瘤进展和骨转移形成。具体而言,促骨质疏松症 miRNA 的血清上调以及抗骨质疏松症 miRNA 的血清下调是所有这些肿瘤的共同特征,能够促进骨转移。这些结果至关重要,有助于研究人员和临床医生建立与循环 miRNA 失调相关的新治疗策略,并能够干扰骨质疏松症、肿瘤进展和骨转移形成的致病过程。