Loryn M Phillips, C. A. Johnston, S. Belinsky, M. Tessema
{"title":"Abstract 2081: Transcriptional silencing of CDK18 in BRG1 mutant lung cancer","authors":"Loryn M Phillips, C. A. Johnston, S. Belinsky, M. Tessema","doi":"10.1158/1538-7445.AM2021-2081","DOIUrl":null,"url":null,"abstract":"In ~10% of lung cancers, the BRG1 gene is mutated often causing a loss of function (LOF). BRG1 is a tumor suppressor that encodes a protein (SMARCA4), which is one of the mutually exclusive ATPase subunits of the Switch/Sucrose Non-fermentable (SWI/SNF) complex. The SWI/SNF complex functions to regulate transcription of many genes including tumor suppressor genes, through mediating chromatin remodeling and nucleosome repositioning by maintaining open chromatin and actively evicting polycomb repressive complexes (PRCs) from target genes and regions. Our previous research showed that BRG1 mutation occurs in approximately 9% of lung adenocarcinomas in smokers and 11% in smokers delineating BRG1 as a clinically relevant mutation. The goal of these studies is to elucidate the downstream effects of BRG1 LOF on gene expression. RNA sequencing of isogenic BRG1 wild type (WT) and knock out (KO) clones from malignant and transformed cell lines identified cell cycle control and chromosomal replication as the most significantly affected pathway. qRT-PCR was used to validate expression changes in 17 genes from this pathway in the WT and KO clones as well as wild type and mutant tumors lines. CDK18 was the most significantly affected target exhibiting a 78% reduction in expression (p Citation Format: Loryn Michelle Phillips, Christopher A. Johnston, Steven A. Belinsky, Mathewos Tessema. Transcriptional silencing of CDK18 in BRG1 mutant lung cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2081.","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"47 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and Cellular Biology / Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/1538-7445.AM2021-2081","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In ~10% of lung cancers, the BRG1 gene is mutated often causing a loss of function (LOF). BRG1 is a tumor suppressor that encodes a protein (SMARCA4), which is one of the mutually exclusive ATPase subunits of the Switch/Sucrose Non-fermentable (SWI/SNF) complex. The SWI/SNF complex functions to regulate transcription of many genes including tumor suppressor genes, through mediating chromatin remodeling and nucleosome repositioning by maintaining open chromatin and actively evicting polycomb repressive complexes (PRCs) from target genes and regions. Our previous research showed that BRG1 mutation occurs in approximately 9% of lung adenocarcinomas in smokers and 11% in smokers delineating BRG1 as a clinically relevant mutation. The goal of these studies is to elucidate the downstream effects of BRG1 LOF on gene expression. RNA sequencing of isogenic BRG1 wild type (WT) and knock out (KO) clones from malignant and transformed cell lines identified cell cycle control and chromosomal replication as the most significantly affected pathway. qRT-PCR was used to validate expression changes in 17 genes from this pathway in the WT and KO clones as well as wild type and mutant tumors lines. CDK18 was the most significantly affected target exhibiting a 78% reduction in expression (p Citation Format: Loryn Michelle Phillips, Christopher A. Johnston, Steven A. Belinsky, Mathewos Tessema. Transcriptional silencing of CDK18 in BRG1 mutant lung cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2081.
在约10%的肺癌中,BRG1基因突变经常导致功能丧失(LOF)。BRG1是一种肿瘤抑制因子,编码一种蛋白(SMARCA4),该蛋白是开关/蔗糖不可发酵(SWI/SNF)复合体中互斥的atp酶亚基之一。SWI/SNF复合物通过维持开放的染色质和主动从靶基因和区域驱逐多梳抑制复合物(PRCs),介导染色质重塑和核小体重定位,从而调节包括肿瘤抑制基因在内的许多基因的转录。我们之前的研究表明,BRG1突变发生在吸烟者中约9%的肺腺癌中,吸烟者中约11%,这表明BRG1是一种临床相关突变。这些研究的目的是阐明BRG1 LOF对基因表达的下游影响。来自恶性和转化细胞系的等基因BRG1野生型(WT)和敲除(KO)克隆的RNA测序发现,细胞周期控制和染色体复制是受影响最显著的途径。采用qRT-PCR验证了该通路17个基因在WT和KO克隆以及野生型和突变型肿瘤细胞系中的表达变化。CDK18是受影响最显著的靶标,表达量减少了78% (p引用格式:Loryn Michelle Phillips, Christopher a. Johnston, Steven a. Belinsky, Mathewos Tessema)。BRG1突变型肺癌中CDK18的转录沉默[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第2081期。