Suppr超能文献

生长抑制因子(ING)基因在非小细胞肺癌中的生物学及临床相关性

The Biological and Clinical Relevance of Inhibitor of Growth (ING) Genes in Non-Small Cell Lung Cancer.

作者信息

Smolle Elisabeth, Fink-Neuboeck Nicole, Lindenmann Joerg, Smolle-Juettner Freyja, Pichler Martin

机构信息

Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria.

Department of Thoracic Surgery, Medical University of Graz, 8036 Graz, Austria.

出版信息

Cancers (Basel). 2019 Aug 6;11(8):1118. doi: 10.3390/cancers11081118.

Abstract

Carcinogenic mutations allow cells to escape governing mechanisms that commonly inhibit uncontrolled cell proliferation and maintain tightly regulated homeostasis between cell death and survival. Members of the inhibition of growth (ING) family act as tumor suppressors, governing cell cycle, apoptosis and cellular senescence. The molecular mechanism of action of genes, as well as their anchor points in pathways commonly linked to malignant transformation of cells, have been studied with respect to a variety of cancer specimens. This review of the current literature focuses specifically on the action mode of family members in lung cancer. We have summarized data from in vitro and in vivo studies, highlighting the effects of varying levels of expression in cancer cells. Based on the increasing insight into the function of these proteins, the use of family members as clinically useful biomarkers for lung cancer detection and prognosis will probably become routine in everyday clinical practice.

摘要

致癌性突变使细胞能够逃避通常抑制不受控制的细胞增殖并维持细胞死亡与存活之间严格调控的稳态的调控机制。生长抑制(ING)家族成员作为肿瘤抑制因子,调控细胞周期、细胞凋亡和细胞衰老。针对多种癌症标本,已经研究了这些基因的分子作用机制及其在通常与细胞恶性转化相关的通路中的锚定节点。本对当前文献的综述特别关注ING家族成员在肺癌中的作用模式。我们总结了来自体外和体内研究的数据,突出了癌细胞中ING不同表达水平的影响。基于对这些蛋白质功能的深入了解,将ING家族成员用作肺癌检测和预后的临床有用生物标志物可能会在日常临床实践中成为常规做法。

相似文献

1
The Biological and Clinical Relevance of Inhibitor of Growth (ING) Genes in Non-Small Cell Lung Cancer.
Cancers (Basel). 2019 Aug 6;11(8):1118. doi: 10.3390/cancers11081118.
2
Grow-ING, Age-ING and Die-ING: ING proteins link cancer, senescence and apoptosis.
Exp Cell Res. 2006 Apr 15;312(7):951-61. doi: 10.1016/j.yexcr.2006.01.020. Epub 2006 Mar 3.
3
Regulation of p53 by ING family members in suppression of tumor initiation and progression.
Cancer Metastasis Rev. 2012 Jun;31(1-2):55-73. doi: 10.1007/s10555-011-9329-5.
4
Molecular mechanisms of inhibitor of growth (ING) family members in health and malignancy.
Cancer Cell Int. 2022 Sep 2;22(1):272. doi: 10.1186/s12935-022-02693-w.
5
Potential usage of ING family members in cancer diagnostics and molecular therapy.
Curr Drug Targets. 2009 May;10(5):465-76. doi: 10.2174/138945009788185086.
6
The inhibitor of growth (ING) gene family: potential role in cancer therapy.
Curr Cancer Drug Targets. 2008 Jun;8(4):275-84. doi: 10.2174/156800908784533454.
7
Modulators of inhibitor of growth (ING) family expression in development and disease.
Curr Drug Targets. 2009 May;10(5):392-405. doi: 10.2174/138945009788185095.
8
Biological functions of the ING family tumor suppressors.
Cell Mol Life Sci. 2004 Oct;61(19-20):2597-613. doi: 10.1007/s00018-004-4199-4.
9
The fellowships of the INGs.
J Cell Biochem. 2005 Dec 15;96(6):1127-36. doi: 10.1002/jcb.20625.
10
Function of the ING family of PHD proteins in cancer.
Int J Biochem Cell Biol. 2005 May;37(5):1054-65. doi: 10.1016/j.biocel.2004.09.008.

引用本文的文献

2
Cancer Stem Cells-Origins and Biomarkers: Perspectives for Targeted Personalized Therapies.
Front Immunol. 2020 Aug 7;11:1280. doi: 10.3389/fimmu.2020.01280. eCollection 2020.
3
Exploiting ING2 Epigenetic Modulation as a Therapeutic Opportunity for Non-Small Cell Lung Cancer.
Cancers (Basel). 2019 Oct 21;11(10):1601. doi: 10.3390/cancers11101601.

本文引用的文献

1
MicroRNA‑214 upregulates HIF‑1α and VEGF by targeting ING4 in lung cancer cells.
Mol Med Rep. 2019 Jun;19(6):4935-4945. doi: 10.3892/mmr.2019.10170. Epub 2019 Apr 16.
2
ING5 inhibits lung cancer invasion and epithelial-mesenchymal transition by inhibiting the WNT/β-catenin pathway.
Thorac Cancer. 2019 Apr;10(4):848-855. doi: 10.1111/1759-7714.13013. Epub 2019 Feb 27.
4
Down-regulation of miR-500 and miR-628 suppress non-small cell lung cancer proliferation, migration and invasion by targeting ING1.
Biomed Pharmacother. 2018 Dec;108:1628-1639. doi: 10.1016/j.biopha.2018.09.145. Epub 2018 Oct 10.
6
Influence of eukaryotic translation initiation factor 6 on non-small cell lung cancer development and progression.
Eur J Cancer. 2018 Sep;101:165-180. doi: 10.1016/j.ejca.2018.07.001. Epub 2018 Aug 1.
7
The expression and significance of histone lysine methylation in endometrial cancer.
Oncol Lett. 2017 Nov;14(5):6210-6216. doi: 10.3892/ol.2017.6979. Epub 2017 Sep 15.
8
ING5 knockdown enhances migration and invasion of lung cancer cells by inducing EMT via EGFR/PI3K/Akt and IL-6/STAT3 signaling pathways.
Oncotarget. 2017 Apr 21;8(33):54265-54276. doi: 10.18632/oncotarget.17346. eCollection 2017 Aug 15.
9
N-BLR, a primate-specific non-coding transcript leads to colorectal cancer invasion and migration.
Genome Biol. 2017 May 24;18(1):98. doi: 10.1186/s13059-017-1224-0.
10
miR-196b-5p Regulates Colorectal Cancer Cell Migration and Metastases through Interaction with HOXB7 and GALNT5.
Clin Cancer Res. 2017 Sep 1;23(17):5255-5266. doi: 10.1158/1078-0432.CCR-17-0023. Epub 2017 May 22.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验