• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人毛细血管扩张性骨肉瘤癌细胞系中微小RNA表达特征的初步分析

Analysis of a Preliminary microRNA Expression Signature in a Human Telangiectatic Osteogenic Sarcoma Cancer Cell Line.

作者信息

Palmini Gaia, Romagnoli Cecilia, Donati Simone, Zonefrati Roberto, Galli Gianna, Marini Francesca, Iantomasi Teresa, Aldinucci Alessandra, Leoncini Gigliola, Franchi Alessandro, Beltrami Giovanni, Campanacci Domenico Andrea, Capanna Rodolfo, Brandi Maria Luisa

机构信息

Department of Experimental and Clinical Biomedical Sciences, University of Florence, 50134 Florence, Italy.

Central Laboratory, Azienda Ospedaliero-Universitaria Careggi, 50134 Florence, Italy.

出版信息

Int J Mol Sci. 2021 Jan 25;22(3):1163. doi: 10.3390/ijms22031163.

DOI:10.3390/ijms22031163
PMID:33503899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7866083/
Abstract

Telangiectatic osteosarcoma (TOS) is an aggressive variant of osteosarcoma (OS) with distinctive radiographic, gross, microscopic features, and prognostic implications. Despite several studies on OS, we are still far from understanding the molecular mechanisms of TOS. In recent years, many studies have demonstrated not only that microRNAs (miRNAs) are involved in OS tumorigenesis, development, and metastasis, but also that the presence in high-grade types of OS of cancer stem cells (CSCs) plays an important role in tumor progression. Despite these findings, nothing has been described previously about the expression of miRNAs and the presence of CSCs in human TOS. Therefore, we have isolated/characterized a putative CSC cell line from human TOS (TOS-CSCs) and evaluated the expression levels of several miRNAs in TOS-CSCs using real-time quantitative assays. We show, for the first time, the existence of CSCs in human TOS, highlighting the in vitro establishment of this unique stabilized cell line and an identification of a preliminary expression of the miRNA profile, characteristic of TOS-CSCs. These findings represent an important step in the study of the biology of one of the most aggressive variants of OS and the role of miRNAs in TOS-CSC behavior.

摘要

毛细血管扩张性骨肉瘤(TOS)是骨肉瘤(OS)的一种侵袭性变体,具有独特的影像学、大体、显微镜特征及预后意义。尽管对骨肉瘤已有多项研究,但我们对毛细血管扩张性骨肉瘤的分子机制仍知之甚少。近年来,许多研究表明,微小RNA(miRNA)不仅参与骨肉瘤的肿瘤发生、发展和转移,而且高级别骨肉瘤中癌症干细胞(CSC)的存在在肿瘤进展中起重要作用。尽管有这些发现,但此前关于人类毛细血管扩张性骨肉瘤中miRNA的表达及癌症干细胞的存在尚未有描述。因此,我们从人类毛细血管扩张性骨肉瘤中分离/鉴定出一种假定的癌症干细胞系(TOS-CSCs),并使用实时定量分析法评估了TOS-CSCs中几种miRNA的表达水平。我们首次证明了人类毛细血管扩张性骨肉瘤中癌症干细胞的存在,突出了这种独特稳定细胞系的体外建立以及对TOS-CSCs特有的miRNA谱初步表达的鉴定。这些发现代表了对骨肉瘤最具侵袭性变体之一的生物学研究以及miRNA在TOS-CSC行为中的作用研究的重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/46d0aeb2193c/ijms-22-01163-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/3a93b6fa57d6/ijms-22-01163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/da8a5e24f53f/ijms-22-01163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/418cf776cd66/ijms-22-01163-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/41e408669644/ijms-22-01163-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/b54c49924402/ijms-22-01163-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/7e19e7d826d1/ijms-22-01163-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/0f301ed008a5/ijms-22-01163-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/425a2634fe8c/ijms-22-01163-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/50c8e15f327f/ijms-22-01163-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/9dcf280ba8e3/ijms-22-01163-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/625c1e325bb3/ijms-22-01163-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/bcde8801f5a6/ijms-22-01163-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/46d0aeb2193c/ijms-22-01163-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/3a93b6fa57d6/ijms-22-01163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/da8a5e24f53f/ijms-22-01163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/418cf776cd66/ijms-22-01163-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/41e408669644/ijms-22-01163-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/b54c49924402/ijms-22-01163-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/7e19e7d826d1/ijms-22-01163-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/0f301ed008a5/ijms-22-01163-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/425a2634fe8c/ijms-22-01163-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/50c8e15f327f/ijms-22-01163-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/9dcf280ba8e3/ijms-22-01163-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/625c1e325bb3/ijms-22-01163-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/bcde8801f5a6/ijms-22-01163-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c0/7866083/46d0aeb2193c/ijms-22-01163-g013.jpg

相似文献

1
Analysis of a Preliminary microRNA Expression Signature in a Human Telangiectatic Osteogenic Sarcoma Cancer Cell Line.人毛细血管扩张性骨肉瘤癌细胞系中微小RNA表达特征的初步分析
Int J Mol Sci. 2021 Jan 25;22(3):1163. doi: 10.3390/ijms22031163.
2
Genetic and molecular characterization of the human osteosarcoma 3AB-OS cancer stem cell line: a possible model for studying osteosarcoma origin and stemness.人骨肉瘤 3AB-OS 肿瘤干细胞系的遗传和分子特征:研究骨肉瘤起源和干细胞特性的可能模型。
J Cell Physiol. 2013 Jun;228(6):1189-201. doi: 10.1002/jcp.24272.
3
MiR-9 is overexpressed in spontaneous canine osteosarcoma and promotes a metastatic phenotype including invasion and migration in osteoblasts and osteosarcoma cell lines.miR-9在自发性犬骨肉瘤中过表达,并促进包括成骨细胞和骨肉瘤细胞系侵袭和迁移在内的转移表型。
BMC Cancer. 2016 Oct 10;16(1):784. doi: 10.1186/s12885-016-2837-5.
4
MicroRNA-29b-1 impairs in vitro cell proliferation, self‑renewal and chemoresistance of human osteosarcoma 3AB-OS cancer stem cells.MicroRNA-29b-1 可损害人骨肉瘤 3AB-OS 肿瘤干细胞的体外细胞增殖、自我更新和化疗耐药性。
Int J Oncol. 2014 Nov;45(5):2013-23. doi: 10.3892/ijo.2014.2618. Epub 2014 Aug 22.
5
Let-7d miRNA Shows Both Antioncogenic and Oncogenic Functions in Osteosarcoma-Derived 3AB-OS Cancer Stem Cells.Let-7d miRNA 在骨肉瘤源性 3AB-OS 癌症干细胞中表现出既具有抑癌作用又具有致癌作用。
J Cell Physiol. 2016 Aug;231(8):1832-41. doi: 10.1002/jcp.25291. Epub 2016 Jan 28.
6
miRNA profiling identifies deregulated miRNAs associated with osteosarcoma development and time to metastasis in two large cohorts.miRNA 谱分析确定了与骨肉瘤发生和转移时间相关的失调 miRNA,该分析基于两个大型队列。
Mol Oncol. 2018 Jan;12(1):114-131. doi: 10.1002/1878-0261.12154. Epub 2017 Dec 1.
7
Bufalin Inhibits the Differentiation and Proliferation of Cancer Stem Cells Derived from Primary Osteosarcoma Cells through Mir-148a.蟾毒灵通过Mir-148a抑制原发性骨肉瘤细胞来源的癌症干细胞的分化和增殖。
Cell Physiol Biochem. 2015;36(3):1186-96. doi: 10.1159/000430289. Epub 2015 Jun 25.
8
MicroRNA-505 is downregulated in human osteosarcoma and regulates cell proliferation, migration and invasion.微小 RNA-505 在人骨肉瘤中下调,并调节细胞增殖、迁移和侵袭。
Oncol Rep. 2018 Feb;39(2):491-500. doi: 10.3892/or.2017.6142. Epub 2017 Dec 11.
9
Tumor-suppressive microRNA-let-7a inhibits cell proliferation via targeting of E2F2 in osteosarcoma cells.肿瘤抑制性微小RNA-let-7a通过靶向骨肉瘤细胞中的E2F2抑制细胞增殖。
Int J Oncol. 2015 Apr;46(4):1543-50. doi: 10.3892/ijo.2015.2867. Epub 2015 Feb 3.
10
Functional characterisation of osteosarcoma cell lines and identification of mRNAs and miRNAs associated with aggressive cancer phenotypes.成骨肉瘤细胞系的功能特征分析及与侵袭性癌症表型相关的 mRNA 和 miRNA 的鉴定。
Br J Cancer. 2013 Oct 15;109(8):2228-36. doi: 10.1038/bjc.2013.549. Epub 2013 Sep 24.

引用本文的文献

1
Establishment and Molecular Characterization of a Human Stem Cell Line from a Primary Cell Culture Obtained from an Ectopic Calcified Lesion of a Tumoral Calcinosis Patient Carrying a Novel Mutation.从一名携带新突变的肿瘤性钙化患者异位钙化病变获取的原代细胞培养物中建立人干细胞系及其分子特征分析
Genes (Basel). 2025 Feb 24;16(3):263. doi: 10.3390/genes16030263.
2
Feasibility and barriers to rapid establishment of patient-derived primary osteosarcoma cell lines in clinical management.在临床管理中快速建立患者来源的原发性骨肉瘤细胞系的可行性及障碍
iScience. 2024 Jun 19;27(9):110251. doi: 10.1016/j.isci.2024.110251. eCollection 2024 Sep 20.
3

本文引用的文献

1
Inhibition of miR-9 decreases osteosarcoma cell proliferation.抑制 miR-9 可降低骨肉瘤细胞增殖。
Bosn J Basic Med Sci. 2020 May 1;20(2):218-225. doi: 10.17305/bjbms.2019.4434.
2
The miR-141/neuropilin-1 axis is associated with the clinicopathology and contributes to the growth and metastasis of pancreatic cancer.miR-141/神经纤毛蛋白-1轴与临床病理特征相关,并促进胰腺癌的生长和转移。
Cancer Cell Int. 2019 Sep 27;19:248. doi: 10.1186/s12935-019-0963-2. eCollection 2019.
3
MicroRNA-744 promotes carcinogenesis in osteosarcoma through targeting LATS2.
Cancer Stem Cells in Sarcomas: In Vitro Isolation and Role as Prognostic Markers: A Systematic Review.
肉瘤中的癌症干细胞:体外分离及其作为预后标志物的作用:一项系统综述
Cancers (Basel). 2023 Apr 25;15(9):2449. doi: 10.3390/cancers15092449.
微小RNA-744通过靶向LATS2促进骨肉瘤的致癌作用。
Oncol Lett. 2019 Sep;18(3):2523-2529. doi: 10.3892/ol.2019.10530. Epub 2019 Jun 26.
4
MiR-369-3p participates in endometrioid adenocarcinoma via the regulation of autophagy.微小RNA-369-3p通过调控自噬参与子宫内膜样腺癌的发生发展。
Cancer Cell Int. 2019 Jul 11;19:178. doi: 10.1186/s12935-019-0897-8. eCollection 2019.
5
MicroRNA-221 promotes cisplatin resistance in osteosarcoma cells by targeting PPP2R2A.MicroRNA-221 通过靶向 PPP2R2A 促进骨肉瘤细胞对顺铂的耐药性。
Biosci Rep. 2019 Jul 10;39(7). doi: 10.1042/BSR20190198. Print 2019 Jul 31.
6
Clinical significance of tumor miR-21, miR-221, miR-143, and miR-106a as biomarkers in patients with osteosarcoma.肿瘤 miR-21、miR-221、miR-143 和 miR-106a 作为骨肉瘤患者生物标志物的临床意义。
Int J Biol Markers. 2019 Jun;34(2):184-193. doi: 10.1177/1724600819843537. Epub 2019 May 14.
7
miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer.miR-500 通过直接靶向前列腺癌中的 LRP1B 促进细胞增殖。
Biosci Rep. 2019 Apr 5;39(4). doi: 10.1042/BSR20181854. Print 2019 Apr 30.
8
A novel miR-365-3p/EHF/keratin 16 axis promotes oral squamous cell carcinoma metastasis, cancer stemness and drug resistance via enhancing β5-integrin/c-met signaling pathway.一个新的 miR-365-3p/EHF/角蛋白 16 轴通过增强 β5-整合素/c-met 信号通路促进口腔鳞状细胞癌转移、癌症干性和耐药性。
J Exp Clin Cancer Res. 2019 Feb 19;38(1):89. doi: 10.1186/s13046-019-1091-5.
9
Expression of miR-664 and miR-184 on proliferation, apoptosis and migration of osteosarcoma cells.miR-664和miR-184对骨肉瘤细胞增殖、凋亡和迁移的影响
Oncol Lett. 2019 Feb;17(2):1791-1797. doi: 10.3892/ol.2018.9739. Epub 2018 Nov 20.
10
MiR-1 Suppresses Proliferation of Osteosarcoma Cells by Up-regulating p21 PAX3.微小RNA-1通过上调p21和PAX3抑制骨肉瘤细胞增殖。
Cancer Genomics Proteomics. 2019 Jan-Feb;16(1):71-79. doi: 10.21873/cgp.20113.