• 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

Structure of the gene encoding the human cyclin-dependent kinase inhibitor p18 and mutational analysis in breast cancer.

作者信息

Blais A, Labrie Y, Pouliot F, Lachance Y, Labrie C

机构信息

Laboratory of Molecular Endocrinology, CHUL Research Center, University Hospital of Quebec, Canada.

出版信息

Biochem Biophys Res Commun. 1998 Jun 9;247(1):146-53. doi: 10.1006/bbrc.1998.8497.

DOI:10.1006/bbrc.1998.8497
PMID:9636670
Abstract

The cyclin-dependent kinase (CDK) inhibitor p18 blocks progression of the cell cycle by associating with the cyclin D-dependent kinases CDK6 and CDK4. To better understand the regulation of p18 gene expression, we isolated full-length cDNA clones from a human BT-20 breast cancer cell cDNA library. These clones were then used to isolate the human gene from a human genomic DNA library. The human p18 gene spans at least 7.5 kb and is composed of three exons, two of which encode the p18 protein. The genomic clone we isolated contained 5 kb of putative promotor sequence which directed expression of the luciferase reporter gene in transient transfection experiments. The longest cDNA that we isolated from BT-20 cells contained 2103 nucleotides which corresponds to the size of the major RNA transcript detected by Northern analysis in these cells. Transcription start sites mapping to the 5' end of the putative full-length cDNA were identified by ribonuclease protection assays. A novel polymorphism was identified in the 3' untranslated region of BT-20 cell cDNA clones that contained the previously described codon 72 mutation. The codon 72 mutation was also detected in 3 of 35 breast tumors analyzed using a mismatch PCR/RFLP strategy.

摘要

相似文献

1
Structure of the gene encoding the human cyclin-dependent kinase inhibitor p18 and mutational analysis in breast cancer.
Biochem Biophys Res Commun. 1998 Jun 9;247(1):146-53. doi: 10.1006/bbrc.1998.8497.
2
A p18 mutant defective in CDK6 binding in human breast cancer cells.
Cancer Res. 1996 Oct 15;56(20):4586-9.
3
Mutational analysis of the p16 family cyclin-dependent kinase inhibitors p15INK4b and p18INK4c in tumor-derived cell lines and primary tumors.肿瘤衍生细胞系和原发性肿瘤中p16家族细胞周期蛋白依赖性激酶抑制剂p15INK4b和p18INK4c的突变分析。
Oncogene. 1996 Jan 18;12(2):451-5.
4
Identification of functional elements of p18INK4C essential for binding and inhibition of cyclin-dependent kinase (CDK) 4 and CDK6.鉴定p18INK4C中对于结合和抑制细胞周期蛋白依赖性激酶(CDK)4和CDK6至关重要的功能元件。
Cancer Res. 1999 Feb 1;59(3):558-64.
5
WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.WWOX是一种新的含WW结构域的蛋白质,定位于人类染色体16q23.3 - 24.1,该区域在乳腺癌中经常受到影响。
Cancer Res. 2000 Apr 15;60(8):2140-5.
6
Lack of imprinting of three human cyclin-dependent kinase inhibitor genes.三种人类细胞周期蛋白依赖性激酶抑制基因的印记缺失
Cancer Res. 1997 Mar 1;57(5):926-9.
7
Evidence of a role for the INK4 family of cyclin-dependent kinase inhibitors in ovarian granulosa cell tumors.细胞周期蛋白依赖性激酶抑制剂INK4家族在卵巢颗粒细胞瘤中作用的证据。
Genes Chromosomes Cancer. 2002 Oct;35(2):176-81. doi: 10.1002/gcc.10108.
8
The COOH terminus of p18INK4C distinguishes function from p16INK4A.p18INK4C的羧基末端将其功能与p16INK4A区分开来。
Cancer Res. 2001 May 15;61(10):3863-8.
9
The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.人类Nramp2基因:基因结构、可变剪接、启动子区域及多态性的特征分析
Blood Cells Mol Dis. 1998 Jun;24(2):199-215. doi: 10.1006/bcmd.1998.0186.
10
Genomic organization and promoter analysis of the mouse ADP-ribosylarginine hydrolase gene.小鼠ADP-核糖基精氨酸水解酶基因的基因组结构与启动子分析
Gene. 2005 May 23;351:83-95. doi: 10.1016/j.gene.2005.02.016.

引用本文的文献

1
CIP/KIP and INK4 families as hostages of oncogenic signaling.CIP/KIP和INK4家族作为致癌信号的人质。
Cell Div. 2024 Apr 1;19(1):11. doi: 10.1186/s13008-024-00115-z.
2
Genomic Landscape of Meningiomas.脑膜瘤的基因组景观。
Adv Exp Med Biol. 2023;1416:137-158. doi: 10.1007/978-3-031-29750-2_11.
3
Long Non-coding RNAs With and Efficacy in Preclinical Models of Esophageal Squamous Cell Carcinoma Which Act by a Non-microRNA Sponging Mechanism.长链非编码 RNA 及其在食管鳞癌临床前模型中的作用和疗效,其作用机制是非 miRNA 海绵机制。
Cancer Genomics Proteomics. 2022 Jul-Aug;19(4):372-389. doi: 10.21873/cgp.20327.
4
A Novel HCC Prognosis Predictor EEF1E1 Is Related to Immune Infiltration and May Be Involved in EEF1E1/ATM/p53 Signaling.一种新型肝癌预后预测因子EEF1E1与免疫浸润相关,可能参与EEF1E1/ATM/p53信号通路。
Front Oncol. 2021 Jul 2;11:700972. doi: 10.3389/fonc.2021.700972. eCollection 2021.
5
Effects of Auraptene on IGF-1 Stimulated Cell Cycle Progression in the Human Breast Cancer Cell Line, MCF-7.金松双黄酮对人乳腺癌细胞系MCF-7中胰岛素样生长因子-1刺激的细胞周期进程的影响。
Int J Breast Cancer. 2012;2012:502092. doi: 10.1155/2012/502092. Epub 2012 Dec 18.
6
Upregulation of p18Ink4c expression by oncogenic HPV E6 via p53-miR-34a pathway.致癌型 HPV E6 通过 p53-miR-34a 通路上调 p18Ink4c 的表达。
Int J Cancer. 2011 Sep 15;129(6):1362-72. doi: 10.1002/ijc.25800. Epub 2011 Feb 26.
7
Implications of a RAD54L polymorphism (2290C/T) in human meningiomas as a risk factor and/or a genetic marker.RAD54L基因多态性(2290C/T)在人类脑膜瘤中作为危险因素和/或遗传标志物的意义。
BMC Cancer. 2003 Mar 4;3:6. doi: 10.1186/1471-2407-3-6.
8
Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas.非典型性和间变性脑膜瘤中肿瘤抑制基因CDKN2A(p16(INK4a))、p14(ARF)、CDKN2B(p15(INK4b))和CDKN2C(p18(INK4c))的改变。
Am J Pathol. 2001 Aug;159(2):661-9. doi: 10.1016/S0002-9440(10)61737-3.
9
Frequent loss of 1p32 region but no mutation of the p18 tumor suppressor gene in meningiomas.脑膜瘤中1p32区域频繁缺失,但p18肿瘤抑制基因无突变。
J Neurooncol. 2000 Dec;50(3):207-13. doi: 10.1023/a:1006400723490.
10
Homozygous deletions of the CDKN2C/p18INK4C gene on the short arm of chromosome 1 in anaplastic oligodendrogliomas.间变性少突胶质细胞瘤中1号染色体短臂上CDKN2C/p18INK4C基因的纯合缺失。
Brain Pathol. 1999 Oct;9(4):639-43. doi: 10.1111/j.1750-3639.1999.tb00545.x.