Suppr超能文献

黑暗面的作用:SMYD3在胃肠道恶性肿瘤中充当癌症基因组守护者。

Playing on the Dark Side: SMYD3 Acts as a Cancer Genome Keeper in Gastrointestinal Malignancies.

作者信息

Sanese Paola, Fasano Candida, Simone Cristiano

机构信息

Medical Genetics, National Institute for Gastroenterology, IRCCS "S. de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.

Medical Genetics, Department of Biomedical Sciences and Human Oncology (DIMO), University of Bari Aldo Moro, 70124 Bari, Italy.

出版信息

Cancers (Basel). 2021 Sep 2;13(17):4427. doi: 10.3390/cancers13174427.

Abstract

The SMYD3 methyltransferase has been found overexpressed in several types of cancers of the gastrointestinal (GI) tract. While high levels of SMYD3 have been positively correlated with cancer progression in cellular and advanced mice models, suggesting it as a potential risk and prognosis factor, its activity seems dispensable for autonomous in vitro cancer cell proliferation. Here, we present an in-depth analysis of SMYD3 functional role in the regulation of GI cancer progression. We first describe the oncogenic activity of SMYD3 as a transcriptional activator of genes involved in tumorigenesis, cancer development and transformation and as a co-regulator of key cancer-related pathways. Then, we dissect its role in orchestrating cell cycle regulation and DNA damage response (DDR) to genotoxic stress by promoting homologous recombination (HR) repair, thereby sustaining cancer cell genomic stability and tumor progression. Based on this evidence and on the involvement of PARP1 in other DDR mechanisms, we also outline a synthetic lethality approach consisting of the combined use of SMYD3 and PARP inhibitors, which recently showed promising therapeutic potential in HR-proficient GI tumors expressing high levels of SMYD3. Overall, these findings identify SMYD3 as a promising target for drug discovery.

摘要

SMYD3甲基转移酶已被发现在几种胃肠道(GI)癌症中过表达。虽然在细胞和晚期小鼠模型中,高水平的SMYD3与癌症进展呈正相关,这表明它是一个潜在的风险和预后因素,但其活性对于体外癌细胞自主增殖似乎并非必需。在此,我们对SMYD3在胃肠道癌症进展调控中的功能作用进行了深入分析。我们首先描述了SMYD3作为参与肿瘤发生、癌症发展和转化的基因的转录激活因子以及关键癌症相关通路的共调节因子的致癌活性。然后,我们剖析了它在协调细胞周期调控和对基因毒性应激的DNA损伤反应(DDR)中的作用,即通过促进同源重组(HR)修复,从而维持癌细胞基因组稳定性和肿瘤进展。基于这些证据以及PARP1在其他DDR机制中的参与,我们还概述了一种合成致死方法,该方法包括联合使用SMYD3和PARP抑制剂,最近在表达高水平SMYD3的HR功能正常的胃肠道肿瘤中显示出有前景的治疗潜力。总体而言,这些发现确定SMYD3是一个有前景的药物研发靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/217c/8430692/b227e5814557/cancers-13-04427-g001.jpg

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