• 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

恶性黑色素瘤干细胞的HDAC9/p300/F-肌动蛋白免疫表达及迁移分析

HDAC9/p300/F-actin immunoexpression and migration analysis for malignant melanoma stem cell.

作者信息

Ozdemir Merve, Ozdil Berrin, Abdikan Cemile Sinem Asker, Erisik Derya, Yesin Taha Kadir, Avci Cıgır Biray, Kurkutçu Yesim, Guler Gunnur, Aktug Huseyin

机构信息

Department of Histology and Embryology, Faculty of Medicine, Ege University, Izmir 35100, Turkey.

Department of Histology and Embryology, Faculty of Medicine, Ege University, Izmir 35100, Turkey; Department of Histology and Embryology, Faculty of Medicine, Suleyman Demirel University, Isparta 32260, Turkey.

出版信息

Pathol Res Pract. 2023 Oct;250:154829. doi: 10.1016/j.prp.2023.154829. Epub 2023 Sep 22.

DOI:10.1016/j.prp.2023.154829
PMID:37748211
Abstract

Melanoma is an aggressive tumor with a poor prognosis that worsens in the metastatic phase. Distruptions of epigenetic mechanisms is known to effect cancer stem cells (CSCs) activity. Malignant melanoma (MM) progression may be promoted by changes in the genetic structure of CSC. Thus, treatments that target epigenetic modifications could be a promising weapon, especially in melanoma. Here, we compared p300, HDAC9, and F-actin proteins in melanoma CSCs (CD133+), non-CSCs (CD133-) and CHL-1 cell line, as well as cell migration and division rates. At 4 and 6 h, P300 protein levels in CHL-1 and CD133 + were remarkably similar, and the CD133- showed increases in expression levels as the incubation period lengthened. HDAC9 protein intensity decreased in CHL-1, increased in the CD133-, and remained relatively unchanged in the CD133+ as the incubation period lengthened. The mean value of F-actin expression level increased in all cell group with time, when the highest increase observed in CHL-1. In conclusion, our studies contribute to the management of metastatic diseases in the future and offer new insight into the molecular basis of the initiation and progression of MM.

摘要

黑色素瘤是一种侵袭性肿瘤,预后较差,在转移阶段会恶化。已知表观遗传机制的破坏会影响癌症干细胞(CSCs)的活性。恶性黑色素瘤(MM)的进展可能由CSC基因结构的变化所促进。因此,针对表观遗传修饰的治疗可能是一种有前景的武器,尤其是在黑色素瘤治疗中。在这里,我们比较了黑色素瘤CSCs(CD133+)、非CSCs(CD133-)和CHL-1细胞系中p300、HDAC9和F-肌动蛋白蛋白,以及细胞迁移和分裂率。在4小时和6小时时,CHL-1和CD133+中的P300蛋白水平非常相似,而CD133-随着孵育时间的延长表达水平增加。随着孵育时间的延长,CHL-1中HDAC9蛋白强度降低,CD133-中增加,而CD133+中相对保持不变。随着时间的推移,所有细胞组中F-肌动蛋白表达水平的平均值均增加,其中CHL-1中增加最为明显。总之,我们的研究有助于未来转移性疾病的管理,并为MM的发生和进展的分子基础提供了新的见解。

相似文献

1
HDAC9/p300/F-actin immunoexpression and migration analysis for malignant melanoma stem cell.恶性黑色素瘤干细胞的HDAC9/p300/F-肌动蛋白免疫表达及迁移分析
Pathol Res Pract. 2023 Oct;250:154829. doi: 10.1016/j.prp.2023.154829. Epub 2023 Sep 22.
2
The Pinx1 Gene Downregulates Telomerase and Inhibits Proliferation of CD133+ Cancer Stem Cells Isolated from a Nasopharyngeal Carcinoma Cell Line by Regulating Trfs and Mad1/C-Myc/p53 Pathways.Pinx1基因通过调控Trfs和Mad1/C-Myc/p53信号通路下调端粒酶并抑制从鼻咽癌细胞系分离出的CD133+癌干细胞的增殖。
Cell Physiol Biochem. 2018;49(1):282-294. doi: 10.1159/000492878. Epub 2018 Aug 23.
3
Decrease of ZEB1 expression inhibits the B16F10 cancer stem-like properties.ZEB1表达的降低抑制了B16F10癌症干细胞样特性。
Biosci Trends. 2015 Oct;9(5):325-34. doi: 10.5582/bst.2015.01106.
4
Effect of HDAC9 inhibition on epithelial-mesenchymal transition in CD133+ prostate cancer cell lines.HDAC9抑制对CD133 +前列腺癌细胞系上皮-间质转化的影响
J Chemother. 2022 Feb;34(1):45-54. doi: 10.1080/1120009X.2021.1963615. Epub 2021 Aug 23.
5
Functional features of cancer stem cells in melanoma cell lines.黑色素瘤细胞系中癌症干细胞的功能特征。
Cancer Cell Int. 2013 Aug 6;13(1):78. doi: 10.1186/1475-2867-13-78.
6
The expression of HDAC9 and P300 in papillary thyroid carcinoma cell line.在甲状腺乳头状癌细胞系中 HDAC9 和 P300 的表达。
Pathol Res Pract. 2023 Mar;243:154385. doi: 10.1016/j.prp.2023.154385. Epub 2023 Feb 24.
7
Patient derived cell culture and isolation of CD133⁺ putative cancer stem cells from melanoma.源自患者的细胞培养以及从黑色素瘤中分离CD133⁺假定癌症干细胞
J Vis Exp. 2013 Mar 13(73):e50200. doi: 10.3791/50200.
8
Differences and Similarities between Colorectal Cancer Cells and Colorectal Cancer Stem Cells: Molecular Insights and Implications.结直肠癌细胞与结直肠癌干细胞之间的异同:分子见解与启示
ACS Omega. 2023 Aug 9;8(33):30145-30157. doi: 10.1021/acsomega.3c02681. eCollection 2023 Aug 22.
9
HERV-K activation is strictly required to sustain CD133+ melanoma cells with stemness features.HERV-K激活是维持具有干性特征的CD133+黑色素瘤细胞所必需的。
J Exp Clin Cancer Res. 2017 Jan 26;36(1):20. doi: 10.1186/s13046-016-0485-x.
10
MicroRNA-92 Expression in CD133 Melanoma Stem Cells Regulates Immunosuppression in the Tumor Microenvironment via Integrin-Dependent Activation of TGFβ.miR-92 在 CD133+ 黑色素瘤干细胞中的表达通过整合素依赖性激活 TGFβ 调节肿瘤微环境中的免疫抑制。
Cancer Res. 2019 Jul 15;79(14):3622-3635. doi: 10.1158/0008-5472.CAN-18-2659. Epub 2019 Apr 23.

引用本文的文献

1
Vibrational spectroscopy unveils distinct cell cycle features of cancer stem cells in melanoma.振动光谱揭示了黑色素瘤中癌症干细胞独特的细胞周期特征。
Sci Rep. 2025 Aug 5;15(1):28494. doi: 10.1038/s41598-025-14018-8.