• 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

正常、转化及恶性人乳腺上皮细胞中多种FGF1 mRNA的表达及其受血清的调控

Expression and regulation by serum of multiple FGF1 mRNA in normal transformed, and malignant human mammary epithelial cells.

作者信息

Renaud F, El Yazidi I, Boilly-Marer Y, Courtois Y, Laurent M

机构信息

Laboratoire INSERM U450, Paris, France.

出版信息

Biochem Biophys Res Commun. 1996 Feb 27;219(3):679-85. doi: 10.1006/bbrc.1996.0294.

DOI:10.1006/bbrc.1996.0294
PMID:8645241
Abstract

In normal (NMEC), transformed (HBL-100) and malignant human mammary epithelial cells (MCF 7, BT-20, MDA-MB 231), we have examined the expression and the regulation by serum of FGF1 and FGF2 mRNA. FGF2 mRNA level was higher in NMEC and in a HBL-100 than in malignant cell lines (MDA-MB-231, BT-20). No FGF2 mRNA was detected in the malignant cell line, MCF-7. In contrast, the FGF1 mRNA was detected in all the mammary epithelial cells but at different levels. NMEC, HBL-100 and MDA-MB231 cells expressed similar level of FGF1 and higher than that observed in BT-20 and MCF-7. In contrast to FGF2 which is only expressed in nonmalignant cells, no correlation between FGF1 mRNA expression and the phenotype of the cells was observed. We followed the expression of four FGF1 mRNA, heterogenous in their 5' untranslated regions. This study demonstrated that (i) the FGF1 mRNA 1.A was not expressed by mammary epithelial cells, (ii) the FGF1 mRNA 1.B was only expressed in normal mammary epithelial cells and (iii) the transcripts 1.C and 1.D were expressed in normal and malignant cells with specific patterns. The expression of FGF1 mRNAs responded in a cell specific manner to serum starvation. The mRNA 1.A was only expressed in normal cells cultured in the absence of serum while 1.C was either up- or down-regulated by serum in transformed cells and the expression of 1.D was greater in presence of serum in all cell lines. These results show that the regulation of FGF1 mRNAs expression is cell specific and does not correlate with a tumorigenic or transformed cell phenotype.

摘要

在正常(NMEC)、转化(HBL - 100)和恶性人乳腺上皮细胞(MCF 7、BT - 20、MDA - MB 231)中,我们检测了FGF1和FGF2 mRNA的表达及其受血清的调控情况。FGF2 mRNA水平在NMEC和HBL - 100中高于恶性细胞系(MDA - MB - 231、BT - 20)。在恶性细胞系MCF - 7中未检测到FGF2 mRNA。相反,在所有乳腺上皮细胞中均检测到FGF1 mRNA,但水平不同。NMEC、HBL - 100和MDA - MB231细胞表达的FGF1水平相似,且高于BT - 20和MCF - 7中的水平。与仅在非恶性细胞中表达的FGF2不同,未观察到FGF1 mRNA表达与细胞表型之间的相关性。我们追踪了四种FGF1 mRNA的表达情况,它们在5'非翻译区存在异质性。这项研究表明:(i)乳腺上皮细胞不表达FGF1 mRNA 1.A;(ii)FGF1 mRNA 1.B仅在正常乳腺上皮细胞中表达;(iii)转录本1.C和1.D在正常和恶性细胞中以特定模式表达。FGF1 mRNA的表达以细胞特异性方式对血清饥饿作出反应。mRNA 1.A仅在无血清培养的正常细胞中表达,而在转化细胞中,1.C受血清上调或下调,且在所有细胞系中,1.D在有血清时表达量更高。这些结果表明,FGF1 mRNA表达的调控具有细胞特异性,与致瘤或转化细胞表型无关。

相似文献

1
Expression and regulation by serum of multiple FGF1 mRNA in normal transformed, and malignant human mammary epithelial cells.正常、转化及恶性人乳腺上皮细胞中多种FGF1 mRNA的表达及其受血清的调控
Biochem Biophys Res Commun. 1996 Feb 27;219(3):679-85. doi: 10.1006/bbrc.1996.0294.
2
Expression of multiple species of basic fibroblast growth factor mRNA and protein in normal and tumor-derived mammary epithelial cells in culture.培养的正常及肿瘤来源乳腺上皮细胞中多种碱性成纤维细胞生长因子mRNA和蛋白质的表达
Cell Growth Differ. 1991 Apr;2(4):195-202.
3
Retinoic acid induces expression of the interleukin-1beta gene in cultured normal human mammary epithelial cells and in human breast carcinoma lines.维甲酸可诱导培养的正常人乳腺上皮细胞及人乳腺癌细胞系中白细胞介素-1β基因的表达。
J Cell Physiol. 2002 Nov;193(2):244-52. doi: 10.1002/jcp.10173.
4
Differential expression of elafin in human normal mammary epithelial cells and carcinomas is regulated at the transcriptional level.弹性蛋白酶抑制因子在人正常乳腺上皮细胞和癌组织中的差异表达在转录水平受到调控。
Cancer Res. 1995 Jun 15;55(12):2537-41.
5
Differential regulation of human fibroblast growth factor 1 transcripts provides a distinct mechanism of cell-specific growth factor expression.人类成纤维细胞生长因子1转录本的差异调控提供了细胞特异性生长因子表达的独特机制。
Cell Growth Differ. 1997 Sep;8(9):999-1013.
6
Posttranscriptional regulation of the c-myb proto-oncogene in estrogen receptor-positive breast cancer cells.雌激素受体阳性乳腺癌细胞中c-myb原癌基因的转录后调控
Clin Cancer Res. 1995 Feb;1(2):235-43.
7
Malignant breast epithelium selects for insulin-like growth factor II expression in breast stroma: evidence for paracrine function.恶性乳腺上皮细胞促使乳腺基质中胰岛素样生长因子II表达:旁分泌功能的证据。
Cancer Res. 1995 Jun 1;55(11):2448-54.
8
17 beta-estradiol-regulated expression of protein tyrosine phosphatase gamma gene in cultured human normal breast and breast cancer cells.17β-雌二醇对培养的人正常乳腺细胞和乳腺癌细胞中蛋白酪氨酸磷酸酶γ基因表达的调控
Anticancer Res. 2000 Jan-Feb;20(1A):11-9.
9
FGF2-stimulated release of endogenous FGF1 is associated with reduced apoptosis in retinal pigmented epithelial cells.成纤维细胞生长因子2(FGF2)刺激内源性FGF1的释放与视网膜色素上皮细胞凋亡减少有关。
Exp Cell Res. 1997 May 25;233(1):198-206. doi: 10.1006/excr.1997.3542.
10
Production of acidic and basic fibroblast growth factor by the hormone-independent breast cancer cell line MDA-MB-231.激素非依赖性乳腺癌细胞系MDA-MB-231产生酸性和碱性成纤维细胞生长因子。
Anticancer Res. 1995 May-Jun;15(3):783-90.

引用本文的文献

1
Central and Peripheral Administration of Fibroblast Growth Factor 1 Improves Pancreatic Islet Insulin Secretion in Diabetic Mouse Models.成纤维细胞生长因子 1 中枢和外周给药改善糖尿病小鼠模型胰岛胰岛素分泌。
Diabetes. 2019 Jul;68(7):1462-1472. doi: 10.2337/db18-1175. Epub 2019 May 2.
2
FGF1 protects neuroblastoma SH-SY5Y cells from p53-dependent apoptosis through an intracrine pathway regulated by FGF1 phosphorylation.成纤维细胞生长因子1(FGF1)通过由FGF1磷酸化调节的自分泌途径保护神经母细胞瘤SH-SY5Y细胞免受p53依赖性凋亡。
Cell Death Dis. 2017 Aug 31;8(8):e3023. doi: 10.1038/cddis.2017.404.
3
RasGAP Shields Akt from Deactivating Phosphatases in Fibroblast Growth Factor Signaling but Loses This Ability Once Cleaved by Caspase-3.
RasGAP可保护Akt免受成纤维细胞生长因子信号传导中失活磷酸酶的作用,但一旦被半胱天冬酶-3切割,便会失去此能力。
J Biol Chem. 2015 Aug 7;290(32):19653-65. doi: 10.1074/jbc.M115.644633. Epub 2015 Jun 24.