• 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

新型高转移活性胰腺癌细胞系的基因表达和甲基化谱的综合分析。

Integrated analysis of gene expression and methylation profiles of novel pancreatic cancer cell lines with highly metastatic activity.

机构信息

Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.

Department of Nuclear Medicine, Peking Union Medical Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.

出版信息

Sci China Life Sci. 2019 Jun;62(6):791-806. doi: 10.1007/s11427-018-9495-2. Epub 2019 Mar 13.

DOI:10.1007/s11427-018-9495-2
PMID:30900162
Abstract

Pancreatic cancer is one of the most lethal human malignancies, partly because of its propensity for metastasis. However, highly metastatic human pancreatic cancer cell lines suitable for studies of metastasis are currently lacking. Here we established two highly metastatic human pancreatic cancer cell lines, MIA PaCa-2 In8 and Panc-1 In8, by Matrigel induction assay. The cell lines were further characterized both in vitro and in vivo. MIA PaCa-2 In8 and Panc-1 In8 cells demonstrated increased migration and invasion compared with their respective parental cells. Following injection into nude mice, MIA PaCa-2 In8 and Panc-1 In8 cells resulted in more pulmonary metastases compared with the parental cells. Furthermore, analyses of mRNA, long non-coding RNA, micro RNA, and methylation profiling revealed that these factors were aberrantly regulated in the highly metastatic cells, indicating that they probably affected metastasis. We thus established and characterized two highly metastatic human pancreatic cell lines that could be used as valuable tools for future investigations into the pathogenesis, metastasis, and potential treatment of human pancreatic cancer.

摘要

胰腺癌是最致命的人类恶性肿瘤之一,部分原因是其易于转移。然而,目前缺乏适合转移研究的高度转移性人胰腺癌细胞系。在这里,我们通过 Matrigel 诱导实验建立了两个高度转移性的人胰腺癌细胞系,MIA PaCa-2 In8 和 Panc-1 In8。我们进一步对这些细胞系进行了体内外的特征描述。与各自的亲本细胞相比,MIA PaCa-2 In8 和 Panc-1 In8 细胞表现出更强的迁移和侵袭能力。将这些细胞系注射到裸鼠体内后,与亲本细胞相比,MIA PaCa-2 In8 和 Panc-1 In8 细胞导致更多的肺转移。此外,对 mRNA、长非编码 RNA、microRNA 和甲基化谱的分析表明,这些因子在高度转移性细胞中异常调节,表明它们可能影响转移。因此,我们建立并鉴定了两个高度转移性的人胰腺癌细胞系,它们可以作为未来研究人类胰腺癌发病机制、转移和潜在治疗的有价值的工具。

相似文献

1
Integrated analysis of gene expression and methylation profiles of novel pancreatic cancer cell lines with highly metastatic activity.新型高转移活性胰腺癌细胞系的基因表达和甲基化谱的综合分析。
Sci China Life Sci. 2019 Jun;62(6):791-806. doi: 10.1007/s11427-018-9495-2. Epub 2019 Mar 13.
2
Identification of a key molecular regulator of liver metastasis in human pancreatic carcinoma using a novel quantitative model of metastasis in NOD/SCID/gammacnull (NOG) mice.利用NOD/SCID/γc基因敲除(NOG)小鼠的新型转移定量模型鉴定人胰腺癌肝转移的关键分子调节因子。
Int J Oncol. 2007 Oct;31(4):741-51.
3
Metastatic-associated biological properties and differential gene expression profiles in established highly liver and peritoneal metastatic cell lines of human pancreatic cancer.人胰腺癌已建立的高肝转移和腹膜转移细胞系中的转移相关生物学特性及差异基因表达谱。
J Exp Clin Cancer Res. 2003 Dec;22(4):623-31.
4
Numb/Notch signaling pathway modulation enhances human pancreatic cancer cell radiosensitivity.Numb/Notch信号通路调节增强人胰腺癌细胞的放射敏感性。
Tumour Biol. 2016 Nov;37(11):15145-15155. doi: 10.1007/s13277-016-5311-8. Epub 2016 Sep 27.
5
Small Nucleolar Noncoding RNA SNORA23, Up-Regulated in Human Pancreatic Ductal Adenocarcinoma, Regulates Expression of Spectrin Repeat-Containing Nuclear Envelope 2 to Promote Growth and Metastasis of Xenograft Tumors in Mice.小核仁非编码 RNA SNORA23 在人胰腺导管腺癌中上调,调节核膜 2 中富含 spectrin 重复的表达,促进小鼠异种移植肿瘤的生长和转移。
Gastroenterology. 2017 Jul;153(1):292-306.e2. doi: 10.1053/j.gastro.2017.03.050. Epub 2017 Apr 5.
6
Silencing of long noncoding RNA LINC00958 prevents tumor initiation of pancreatic cancer by acting as a sponge of microRNA-330-5p to down-regulate PAX8.长链非编码 RNA LINC00958 通过作为 microRNA-330-5p 的海绵来下调 PAX8 从而防止胰腺癌的肿瘤发生。
Cancer Lett. 2019 Apr 1;446:49-61. doi: 10.1016/j.canlet.2018.12.017. Epub 2019 Jan 9.
7
KAI1 inhibits lymphangiogenesis and lymphatic metastasis of pancreatic cancer in vivo.KAI1在体内抑制胰腺癌的淋巴管生成和淋巴转移。
Hepatobiliary Pancreat Dis Int. 2014 Feb;13(1):87-92. doi: 10.1016/s1499-3872(14)60012-6.
8
[MiR-150-5p inhibits the proliferation and promoted apoptosis of pancreatic cancer cells].[微小RNA-150-5p抑制胰腺癌细胞增殖并促进其凋亡]
Zhonghua Bing Li Xue Za Zhi. 2013 Jul;42(7):460-4. doi: 10.3760/cma.j.issn.0529-5807.2013.07.007.
9
Nerve growth factor exerts differential effects on the growth of human pancreatic cancer cells.神经生长因子对人胰腺癌细胞的生长具有不同的作用。
Clin Cancer Res. 2001 Jan;7(1):105-12.
10
Long noncoding RNA NORAD, a novel competing endogenous RNA, enhances the hypoxia-induced epithelial-mesenchymal transition to promote metastasis in pancreatic cancer.长链非编码 RNA NORAD,一种新型的竞争性内源性 RNA,增强了缺氧诱导的上皮-间充质转化,促进了胰腺癌的转移。
Mol Cancer. 2017 Nov 9;16(1):169. doi: 10.1186/s12943-017-0738-0.

引用本文的文献

1
Epigenetic reprogramming-induced guanidinoacetic acid synthesis promotes pancreatic cancer metastasis and transcription-activating histone modifications.表观遗传重编程诱导胍基乙酸合成促进胰腺癌转移和转录激活组蛋白修饰。
J Exp Clin Cancer Res. 2023 Jun 28;42(1):155. doi: 10.1186/s13046-023-02698-x.
2
CBP-mediated Slug acetylation stabilizes Slug and promotes EMT and migration of breast cancer cells.CBP 介导的 Slug 乙酰化稳定 Slug 并促进乳腺癌细胞的 EMT 和迁移。
Sci China Life Sci. 2021 Apr;64(4):563-574. doi: 10.1007/s11427-020-1736-5. Epub 2020 Jul 29.
3
Hexosamine pathway inhibition overcomes pancreatic cancer resistance to gemcitabine through unfolded protein response and EGFR-Akt pathway modulation.
己糖胺途径抑制通过未折叠蛋白反应和 EGFR-Akt 通路调节克服胰腺癌对吉西他滨的耐药性。
Oncogene. 2020 May;39(20):4103-4117. doi: 10.1038/s41388-020-1260-1. Epub 2020 Mar 31.