• 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

在结直肠癌发生过程中,[基因名称1]、[基因名称2]和[基因名称3]的等位基因转换

Allelic Switching of , , and during Colorectal Cancer Tumorigenesis.

作者信息

Boot Arnoud, Oosting Jan, Doorn Saskia, Ouahoud Sarah, Ventayol Garcia Marina, Ruano Dina, Morreau Hans, van Wezel Tom

机构信息

Department of Pathology, Leiden University Medical Center, Leiden, Netherlands.

出版信息

Int J Genomics. 2019 Apr 10;2019:1287671. doi: 10.1155/2019/1287671. eCollection 2019.

DOI:10.1155/2019/1287671
PMID:31093489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6481143/
Abstract

Allele-specific expression (ASE) is found in approximately 20-30% of human genes. During tumorigenesis, ASE changes due to somatic alterations that change the regulatory landscape. In colorectal cancer (CRC), many chromosomes show frequent gains or losses while homozygosity of chromosome 7 is rare. We hypothesized that genes essential to survival show allele-specific expression (ASE) on both alleles of chromosome 7. Using a panel of 21 recently established low-passage CRC cell lines, we performed ASE analysis by hybridizing DNA and cDNA to Infinium HumanExome-12 v1 BeadChips containing cSNPs in 392 chromosome 7 genes. The results of this initial analysis were extended and validated in a set of 89 paired normal mucosa and CRC samples. We found that 14% of genes showed ASE in one or more cell lines and identified of the potential cell survival genes , , and on chromosome 7, whereby the most abundantly expressed allele in the normal tissue is the lowest expressed allele in the tumor and vice versa. We established that this allelic switch does not result from loss of imprinting. The allelic switching of may be a result of transcriptional downregulation, while the exact mechanisms resulting in the allelic switching of and remain to be elucidated. In conclusion, our results show that profound changes take place in allelic transcriptional regulation during the tumorigenesis of CRC.

摘要

等位基因特异性表达(ASE)在约20%-30%的人类基因中存在。在肿瘤发生过程中,ASE会因改变调控格局的体细胞改变而发生变化。在结直肠癌(CRC)中,许多染色体显示出频繁的获得或缺失,而7号染色体的纯合性则很罕见。我们假设对生存至关重要的基因在7号染色体的两个等位基因上都表现出等位基因特异性表达(ASE)。我们使用一组21个最近建立的低传代CRC细胞系,通过将DNA和cDNA与包含392个7号染色体基因中cSNP的Infinium HumanExome-12 v1 BeadChips杂交来进行ASE分析。这一初步分析的结果在一组89对正常黏膜和CRC样本中得到了扩展和验证。我们发现14%的基因在一个或多个细胞系中表现出ASE,并在7号染色体上鉴定出了潜在的细胞存活基因、和,其中正常组织中表达最丰富的等位基因在肿瘤中是表达最低的等位基因,反之亦然。我们确定这种等位基因转换不是由印记丢失导致的。的等位基因转换可能是转录下调的结果,而导致和等位基因转换的确切机制仍有待阐明。总之,我们的结果表明,在CRC肿瘤发生过程中等位基因转录调控发生了深刻变化。

相似文献

1
Allelic Switching of , , and during Colorectal Cancer Tumorigenesis.在结直肠癌发生过程中,[基因名称1]、[基因名称2]和[基因名称3]的等位基因转换
Int J Genomics. 2019 Apr 10;2019:1287671. doi: 10.1155/2019/1287671. eCollection 2019.
2
Characterizing the allele-specific gene expression landscape in high hyperdiploid acute lymphoblastic leukemia with BASE.利用 BASE 描绘高倍体超二倍体急性淋巴细胞白血病的等位基因特异性基因表达图谱。
Sci Rep. 2024 Oct 5;14(1):23181. doi: 10.1038/s41598-024-73743-8.
3
A Genome-Wide Study of Allele-Specific Expression in Colorectal Cancer.一项关于结直肠癌中基因特异性表达的全基因组研究。
Front Genet. 2018 Nov 27;9:570. doi: 10.3389/fgene.2018.00570. eCollection 2018.
4
Investigation of allele-specific expression of genes involved in adipogenesis and lipid metabolism suggests complex regulatory mechanisms of PPARGC1A expression in porcine fat tissues.对参与脂肪生成和脂质代谢的基因的等位基因特异性表达的研究表明,猪脂肪组织中PPARGC1A表达存在复杂的调控机制。
BMC Genet. 2018 Nov 29;19(1):107. doi: 10.1186/s12863-018-0696-6.
5
Imprinted survival genes preclude loss of heterozygosity of chromosome 7 in cancer cells.印迹存活基因可防止癌细胞中染色体 7 的杂合性丢失。
J Pathol. 2016 Sep;240(1):72-83. doi: 10.1002/path.4756.
6
Genomic imprinting and allelic exclusion.基因组印记与等位基因排斥。
Dev Suppl. 1990:125-9.
7
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.DLX5和DLX6的表达是双等位基因的,且不受MeCP2缺陷的调节。
Am J Hum Genet. 2007 Sep;81(3):492-506. doi: 10.1086/520063. Epub 2007 Aug 2.
8
Methylation associated transcriptional repression of ELOVL5 in novel colorectal cancer cell lines.新型结直肠癌细胞系中ELOVL5的甲基化相关转录抑制
PLoS One. 2017 Sep 20;12(9):e0184900. doi: 10.1371/journal.pone.0184900. eCollection 2017.
9
Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery.家族性胰腺癌患者生殖系中的等位基因特异性表达:一种无偏见的癌症基因发现方法。
Cancer Biol Ther. 2008 Jan;7(1):135-44. doi: 10.4161/cbt.7.1.5199. Epub 2007 Oct 19.
10
Large-scale profiling and identification of potential regulatory mechanisms for allelic gene expression in colorectal cancer cells.大规模分析和鉴定结直肠癌细胞中等位基因表达的潜在调控机制。
Gene. 2013 Jan 1;512(1):16-22. doi: 10.1016/j.gene.2012.10.001. Epub 2012 Oct 10.

引用本文的文献

1
Allelic expression patterns of imprinted and non-imprinted genes in cancer cell lines from multiple histologies.多种组织学来源的癌细胞系中印迹基因和非印迹基因的等位基因表达模式。
Clin Epigenetics. 2025 May 25;17(1):83. doi: 10.1186/s13148-025-01883-3.
2
The Solute Carrier Superfamily as Therapeutic Targets in Pancreatic Ductal Adenocarcinoma.溶质载体超家族作为胰腺导管腺癌的治疗靶点
Genes (Basel). 2025 Apr 18;16(4):463. doi: 10.3390/genes16040463.
3
Genome-wide allele-specific expression in multi-tissue samples from healthy male baboons reveals the transcriptional complexity of mammals.

本文引用的文献

1
Imprinted survival genes preclude loss of heterozygosity of chromosome 7 in cancer cells.印迹存活基因可防止癌细胞中染色体 7 的杂合性丢失。
J Pathol. 2016 Sep;240(1):72-83. doi: 10.1002/path.4756.
2
Allele-specific expression of mutated in colorectal cancer (MCC) gene and alternative susceptibility to colorectal cancer in schizophrenia.结直肠癌中突变的结直肠癌基因(MCC)的等位基因特异性表达与精神分裂症患者患结直肠癌的易感性差异
Sci Rep. 2016 May 26;6:26688. doi: 10.1038/srep26688.
3
Characterization of novel low passage primary and metastatic colorectal cancer cell lines.
来自健康雄性狒狒多组织样本的全基因组等位基因特异性表达揭示了哺乳动物的转录复杂性。
Cell Genom. 2025 May 14;5(5):100823. doi: 10.1016/j.xgen.2025.100823. Epub 2025 Apr 4.
4
Germline variant affecting p53β isoforms predisposes to familial cancer.胚系变异影响 p53β 异构体,易患家族性癌症。
Nat Commun. 2024 Sep 18;15(1):8208. doi: 10.1038/s41467-024-52551-8.
5
Altered methylation of imprinted genes in neuroblastoma: implications for prognostic refinement.神经母细胞瘤中印记基因的甲基化改变:对预后细化的影响。
J Transl Med. 2024 Aug 31;22(1):808. doi: 10.1186/s12967-024-05634-5.
6
WGCNA-based identification of potential targets and pathways in response to treatment in locally advanced breast cancer patients.基于加权基因共表达网络分析(WGCNA)鉴定局部晚期乳腺癌患者治疗反应中的潜在靶点和通路。
Open Med (Wars). 2023 Mar 6;18(1):20230651. doi: 10.1515/med-2023-0651. eCollection 2023.
7
Increased copy number of imprinted genes in the chromosomal region 20q11-q13.32 is associated with resistance to antitumor agents in cancer cell lines.20q11-q13.32 染色体区域中印记基因的拷贝数增加与癌细胞系中抗肿瘤药物耐药性有关。
Clin Epigenetics. 2022 Dec 2;14(1):161. doi: 10.1186/s13148-022-01368-7.
新型低传代原发性和转移性结肠癌细胞系的特征分析
Oncotarget. 2016 Mar 22;7(12):14499-509. doi: 10.18632/oncotarget.7391.
4
Dlx5 Homeodomain:DNA Complex: Structure, Binding and Effect of Mutations Related to Split Hand and Foot Malformation Syndrome.Dlx5 同源结构域:DNA 复合物:与并指/趾畸形综合征相关的突变的结构、结合及影响
J Mol Biol. 2016 Mar 27;428(6):1130-1141. doi: 10.1016/j.jmb.2016.01.023. Epub 2016 Jan 29.
5
Proper Use of Allele-Specific Expression Improves Statistical Power for -eQTL Mapping with RNA-Seq Data.等位基因特异性表达的正确使用提高了基于RNA测序数据进行表达数量性状基因座定位的统计效力。
J Am Stat Assoc. 2015;110(511):962-974. doi: 10.1080/01621459.2015.1038449. Epub 2015 Nov 7.
6
Genes that Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving.在人类中逃避X染色体失活的基因在表达上具有高度种内变异性,与智力障碍相关,但进化并不缓慢。
Mol Biol Evol. 2016 Jan;33(1):302. doi: 10.1093/molbev/msv180. Epub 2015 Nov 13.
7
Genomic Classification of Cutaneous Melanoma.皮肤黑色素瘤的基因组分类
Cell. 2015 Jun 18;161(7):1681-96. doi: 10.1016/j.cell.2015.05.044.
8
Copy number alterations and allelic ratio in relation to recurrence of rectal cancer.直肠癌复发相关的拷贝数改变和等位基因比率
BMC Genomics. 2015 Jun 6;16(1):438. doi: 10.1186/s12864-015-1550-0.
9
X-chromosome inactivation: new insights into cis and trans regulation.X染色体失活:顺式和反式调控的新见解
Curr Opin Genet Dev. 2015 Apr;31:57-66. doi: 10.1016/j.gde.2015.04.002. Epub 2015 May 22.
10
Recommendations for Accurate Resolution of Gene and Isoform Allele-Specific Expression in RNA-Seq Data.RNA测序数据中基因和异构体等位基因特异性表达精确解析的建议
PLoS One. 2015 May 12;10(5):e0126911. doi: 10.1371/journal.pone.0126911. eCollection 2015.