Consensus reference gene(s) for gene expression studies in human cancers: end of the tunnel visible?

被引:27
作者
Sharan, R. N. [1 ]
Vaiphei, S. Thangminlal [1 ]
Nongrum, Saibadaiahun [1 ]
Keppen, Joshua [1 ]
Ksoo, Mandahakani [1 ]
机构
[1] NE Hill Univ, Dept Biochem, Radiat & Mol Biol Unit, Shillong 793022, Meghalayn, India
关键词
Reference genes; Normalizer genes; Endogenous controls; qPCR; Gene expression; Human cancers; REVERSE TRANSCRIPTION-PCR; REAL-TIME PCR; SUITABLE REFERENCE GENES; ENDOGENOUS CONTROL GENES; RENAL-CELL CARCINOMA; QUANTITATIVE RT-PCR; BREAST-CANCER; MESSENGER-RNA; HOUSEKEEPING GENES; PROSTATE-CANCER;
D O I
10.1007/s13402-015-0244-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Gene expression studies are increasingly used to provide valuable information on the diagnosis and prognosis of human cancers. Also, for in vitro and in vivo experimental cancer models gene expression studies are widely used. The complex algorithms of differential gene expression analyses require normalization of data against a reference or normalizer gene, or a set of such genes. For this purpose, mostly invariant housekeeping genes are used. Unfortunately, however, there are no consensus (housekeeping) genes that serve as reference or normalizer for different human cancers. In fact, scientists have employed a wide range of reference genes across different types of cancer for normalization of gene expression data. As a consequence, comparisons of these data and/or data harmonizations are difficult to perform and challenging. In addition, an inadequate choice for a reference gene may obscure genuine changes and/or result in erroneous gene expression data comparisons. Methods In our effort to highlight the importance of selecting the most appropriate reference gene(s), we have screened the literature for gene expression studies published since the turn of the century on thirteen of the most prevalent human cancers worldwide. Conclusions Based on the analysis of the data at hand, we firstly recommend that in each study the suitability of candidate reference gene(s) should carefully be evaluated in order to yield reliable differential gene expression data. Secondly, we recommend that a combination of PPIA and either GAPDH, ACTB, HPRT and TBP, or appropriate combinations of two or three of these genes, should be employed in future studies, to ensure that results from different studies on different human cancers can be harmonized. This approach will ultimately increase the depth of our understanding of gene expression signatures across human cancers.
引用
收藏
页码:419 / 431
页数:13
相关论文
共 157 条
[1]   Prostate tumor OVerexpressed-1 (PTOV1) down-regulates HES1 and HEY1 notch targets genes and promotes prostate cancer progression [J].
Alana, Lide ;
Sese, Marta ;
Canovas, Veronica ;
Punyal, Yolanda ;
Fernandez, Yolanda ;
Abasolo, Ibane ;
de Torres, Ines ;
Ruiz, Cristina ;
Espinosa, Lluis ;
Bigas, Anna ;
Ramon y Cajal, Santiago ;
Fernandez, Pedro L. ;
Serras, Florenci ;
Corominas, Montserrat ;
Thomson, Timothy M. ;
Paciucci, Rosanna .
MOLECULAR CANCER, 2014, 13
[2]   Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets [J].
Andersen, CL ;
Jensen, JL ;
Orntoft, TF .
CANCER RESEARCH, 2004, 64 (15) :5245-5250
[3]   DTX3L and ARTD9 inhibit IRF1 expression and mediate in cooperation with ARTD8 survival and proliferation of metastatic prostate cancer cells [J].
Bachmann, Samia B. ;
Frommel, Sandra C. ;
Camicia, Rosalba ;
Winkler, Hans C. ;
Santoro, Raffaella ;
Hassa, Paul O. .
MOLECULAR CANCER, 2014, 13
[4]   Down-regulation of FRα Inhibits Proliferation and Promotes Apoptosis of Cervical Cancer Cells in Vitro [J].
Bai, Li-Xia ;
Ding, Ling ;
Jiang, Shi-Wen ;
Kang, Hui-Jie ;
Gao, Chen-Fei ;
Chen, Chen ;
Zhou, Qin ;
Wang, Jin-Tao .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2014, 15 (14) :5667-5672
[5]   Proteomic Profiling of Thyroid Papillary Carcinoma [J].
Ban, Yoshiyuki ;
Yamamoto, Gou ;
Takada, Michiya ;
Hayashi, Shigeo ;
Ban, Yoshio ;
Shimizu, Kazuo ;
Akasu, Haruki ;
Igarashi, Takehito ;
Bando, Yasuhiko ;
Tachikawa, Tetsuhiko ;
Hirano, Tsutomu .
JOURNAL OF THYROID RESEARCH, 2012, 2012
[6]   GAPDH as a housekeeping gene: analysis of GAPDH mRNA expression in a panel of 72 human tissues [J].
Barber, RD ;
Harmer, DW ;
Coleman, RA ;
Clark, BJ .
PHYSIOLOGICAL GENOMICS, 2005, 21 (03) :389-395
[7]   Housekeeping gene variability in normal and carcinomatous colorectal and liver tissues: Applications in pharmacogenomic gene expression studies [J].
Blanquicett, C ;
Johnson, MR ;
Heslin, M ;
Diasio, RB .
ANALYTICAL BIOCHEMISTRY, 2002, 303 (02) :209-214
[8]   Oesophageal adenocarcinoma is associated with a deregulation in the MYC/MAX/MAD network [J].
Boult, J. K. R. ;
Taniere, P. ;
Hallissey, M. T. ;
Campbell, M. J. ;
Tselepis, C. .
BRITISH JOURNAL OF CANCER, 2008, 98 (12) :1985-1992
[9]   The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments [J].
Bustin, Stephen A. ;
Benes, Vladimir ;
Garson, Jeremy A. ;
Hellemans, Jan ;
Huggett, Jim ;
Kubista, Mikael ;
Mueller, Reinhold ;
Nolan, Tania ;
Pfaffl, Michael W. ;
Shipley, Gregory L. ;
Vandesompele, Jo ;
Wittwer, Carl T. .
CLINICAL CHEMISTRY, 2009, 55 (04) :611-622
[10]   Loss of NF2/Merlin expression in advanced sporadic colorectal cancer [J].
Cacev, Tamara ;
Aralica, Gorana ;
Loncar, Bozo ;
Kapitanovic, Sanja .
CELLULAR ONCOLOGY, 2014, 37 (01) :69-77