Copy number variation is highly correlated with differential gene expression: a pan-cancer study

被引:182
作者
Shao, Xin [1 ]
Lv, Ning [1 ]
Liao, Jie [1 ]
Long, Jinbo [1 ]
Xue, Rui [1 ]
Ai, Ni [1 ]
Xu, Donghang [2 ]
Fan, Xiaohui [1 ]
机构
[1] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Pharm, Hangzhou 310009, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Copy number variation; Differential gene expression; Concordance; Pan-cancer; COLORECTAL-CANCER; PROTEIN; OVEREXPRESSION; AMPLIFICATION; TUMORIGENESIS; POLYMORPHISM; METABOLISM; MECHANISMS; DERLIN-1; SEQUENCE;
D O I
10.1186/s12881-019-0909-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Cancer is a heterogeneous disease with many genetic variations. Lines of evidence have shown copy number variations (CNVs) of certain genes are involved in development and progression of many cancers through the alterations of their gene expression levels on individual or several cancer types. However, it is not quite clear whether the correlation will be a general phenomenon across multiple cancer types. Methods In this study we applied a bioinformatics approach integrating CNV and differential gene expression mathematically across 1025 cell lines and 9159 patient samples to detect their potential relationship. Results Our results showed there is a close correlation between CNV and differential gene expression and the copy number displayed a positive linear influence on gene expression for the majority of genes, indicating that genetic variation generated a direct effect on gene transcriptional level. Another independent dataset is utilized to revalidate the relationship between copy number and expression level. Further analysis show genes with general positive linear influence on gene expression are clustered in certain disease-related pathways, which suggests the involvement of CNV in pathophysiology of diseases. Conclusions This study shows the close correlation between CNV and differential gene expression revealing the qualitative relationship between genetic variation and its downstream effect, especially for oncogenes and tumor suppressor genes. It is of a critical importance to elucidate the relationship between copy number variation and gene expression for prevention, diagnosis and treatment of cancer.
引用
收藏
页数:14
相关论文
共 58 条
  • [1] Genetic effects on gene expression across human tissues
    Aguet, Francois
    Brown, Andrew A.
    Castel, Stephane E.
    Davis, Joe R.
    He, Yuan
    Jo, Brian
    Mohammadi, Pejman
    Park, Yoson
    Parsana, Princy
    Segre, Ayellet V.
    Strober, Benjamin J.
    Zappala, Zachary
    Cummings, Beryl B.
    Gelfand, Ellen T.
    Hadley, Kane
    Huang, Katherine H.
    Lek, Monkol
    Li, Xiao
    Nedzel, Jared L.
    Nguyen, Duyen Y.
    Noble, Michael S.
    Sullivan, Timothy J.
    Tukiainen, Taru
    MacArthur, Daniel G.
    Getz, Gad
    Management, Nih Program
    Addington, Anjene
    Guan, Ping
    Koester, Susan
    Little, A. Roger
    Lockhart, Nicole C.
    Moore, Helen M.
    Rao, Abhi
    Struewing, Jeffery P.
    Volpi, Simona
    Collection, Biospecimen
    Brigham, Lori E.
    Hasz, Richard
    Hunter, Marcus
    Johns, Christopher
    Johnson, Mark
    Kopen, Gene
    Leinweber, William F.
    Lonsdale, John T.
    McDonald, Alisa
    Mestichelli, Bernadette
    Myer, Kevin
    Roe, Bryan
    Salvatore, Michael
    Shad, Saboor
    [J]. NATURE, 2017, 550 (7675) : 204 - +
  • [2] The TGF-β/Smad4 Signaling Pathway in Pancreatic Carcinogenesis and Its Clinical Significance
    Ahmed, Sunjida
    Bradshaw, Azore-Dee
    Gera, Shweta
    Dewan, M. Zahidunnabi
    Xu, Ruliang
    [J]. JOURNAL OF CLINICAL MEDICINE, 2017, 6 (01):
  • [3] The Small Molecules Targeting Ubiquitin-Proteasome System for Cancer Therapy
    Ao, Nannan
    Chen, Qianping
    Liu, Geng
    [J]. COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2017, 20 (05) : 403 - 413
  • [4] Aberrant ubiquitin-mediated proteolysis of cell cycle regulatory proteins and oncogenesis
    Bashir, T
    Pagano, M
    [J]. ADVANCES IN CANCER RESEARCH, VOL 88, 2003, 88 : 101 - 144
  • [5] Obesity and Breast Cancer: Current Insights on the Role of Fatty Acids and Lipid Metabolism in Promoting Breast Cancer Growth and Progression
    Bluecher, Christina
    Stadler, Sonja C.
    [J]. FRONTIERS IN ENDOCRINOLOGY, 2017, 8
  • [6] Pan-Cancer Analysis of Copy Number Changes in Programmed Death-Ligand 1 (PD-L1, CD274) - Associations with Gene Expression, Mutational Load, and Survival
    Budczies, Jan
    Bockmayr, Michael
    Denkert, Carsten
    Klauschen, Frederick
    Groeschel, Stefan
    Darb-Esfahani, Silvia
    Pfarr, Nicole
    Leichsenring, Jonas
    Onozato, Maristela L.
    Lennerz, Jochen K.
    Dietel, Manfred
    Froehling, Stefan
    Schirmacher, Peter
    Iafrate, A. John
    Weichert, Wilko
    Stenzinger, Albrecht
    [J]. GENES CHROMOSOMES & CANCER, 2016, 55 (08) : 626 - 639
  • [7] Clinical Implications of FADD Gene Amplification and Protein Overexpression in Taiwanese Oral Cavity Squamous Cell Carcinomas
    Chien, Huei-Tzu
    Cheng, Sou-De
    Chuang, Wen-Yu
    Liao, Chun-Ta
    Wang, Hung-Ming
    Huang, Shiang-Fu
    [J]. PLOS ONE, 2016, 11 (10):
  • [8] A high-resolution survey of deletion polymorphism in the human genome
    Conrad, DF
    Andrews, TD
    Carter, NP
    Hurles, ME
    Pritchard, JK
    [J]. NATURE GENETICS, 2006, 38 (01) : 75 - 81
  • [9] The Immunome of Colon Cancer: Functional In Silico Analysis of Antigenic Proteins Deduced from IgG Microarray Profiling
    Coronell, Johana A. Luna
    Sergelen, Khulan
    Hofer, Philipp
    Gyurjan, Istvan
    Brezina, Stefanie
    Hettegger, Peter
    Leeb, Gernot
    Mach, Karl
    Gsur, Andrea
    Weinhaeusel, Andreas
    [J]. GENOMICS PROTEOMICS & BIOINFORMATICS, 2018, 16 (01) : 73 - 84
  • [10] Functional redundancy between Apc and Apc2 regulates tissue homeostasis and prevents tumorigenesis in murine mammary epithelium
    Daly, C. S.
    Shaw, P.
    Ordonez, L. D.
    Williams, G. T.
    Quist, J.
    Grigoriadis, A.
    Van Es, J. H.
    Clevers, H.
    Clarke, A. R.
    Reed, K. R.
    [J]. ONCOGENE, 2017, 36 (13) : 1793 - 1803