» Articles » PMID: 21356087

Assessing Quality and Completeness of Human Transcriptional Regulatory Pathways on a Genome-wide Scale

Overview
Journal Biol Direct
Publisher Biomed Central
Specialty Biology
Date 2011 Mar 2
PMID 21356087
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Pathway databases are becoming increasingly important and almost omnipresent in most types of biological and translational research. However, little is known about the quality and completeness of pathways stored in these databases. The present study conducts a comprehensive assessment of transcriptional regulatory pathways in humans for seven well-studied transcription factors: MYC, NOTCH1, BCL6, TP53, AR, STAT1, and RELA. The employed benchmarking methodology first involves integrating genome-wide binding with functional gene expression data to derive direct targets of transcription factors. Then the lists of experimentally obtained direct targets are compared with relevant lists of transcriptional targets from 10 commonly used pathway databases.

Results: The results of this study show that for the majority of pathway databases, the overlap between experimentally obtained target genes and targets reported in transcriptional regulatory pathway databases is surprisingly small and often is not statistically significant. The only exception is MetaCore pathway database which yields statistically significant intersection with experimental results in 84% cases. Additionally, we suggest that the lists of experimentally derived direct targets obtained in this study can be used to reveal new biological insight in transcriptional regulation and suggest novel putative therapeutic targets in cancer.

Conclusions: Our study opens a debate on validity of using many popular pathway databases to obtain transcriptional regulatory targets. We conclude that the choice of pathway databases should be informed by solid scientific evidence and rigorous empirical evaluation.

Reviewers: This article was reviewed by Prof. Wing Hung Wong, Dr. Thiago Motta Venancio (nominated by Dr. L Aravind), and Prof. Geoff J McLachlan.

Citing Articles

Gene network screening of bladder cancer via modular analysis.

Li X, Wu Y, Yuan Y Transl Cancer Res. 2022; 10(2):1043-1052.

PMID: 35116431 PMC: 8798099. DOI: 10.21037/tcr-20-2822.


Modulation of stress and immune response by Amblyomin-X results in tumor cell death in a horse melanoma model.

Lichtenstein F, Iqbal A, de Lima Will S, Bosch R, DeOcesano-Pereira C, Goldfeder M Sci Rep. 2020; 10(1):6388.

PMID: 32286411 PMC: 7156751. DOI: 10.1038/s41598-020-63275-2.


Integrated nuclear proteomics and transcriptomics identifies S100A4 as a therapeutic target in acute myeloid leukemia.

Alanazi B, Munje C, Rastogi N, Williamson A, Taylor S, Hole P Leukemia. 2019; 34(2):427-440.

PMID: 31611628 PMC: 6995695. DOI: 10.1038/s41375-019-0596-4.


Analyses of Skin and Peripheral Blood Transcriptional Data in Cutaneous Lupus Reveals CCR2-A Novel Potential Therapeutic Target.

Dey-Rao R, Sinha A Front Immunol. 2019; 10:640.

PMID: 30984198 PMC: 6450170. DOI: 10.3389/fimmu.2019.00640.


Identification of pharmacodynamic biomarker hypotheses through literature analysis with IBM Watson.

Hatz S, Spangler S, Bender A, Studham M, Haselmayer P, Lacoste A PLoS One. 2019; 14(4):e0214619.

PMID: 30958864 PMC: 6453528. DOI: 10.1371/journal.pone.0214619.


References
1.
Basso K, Saito M, Sumazin P, Margolin A, Wang K, Lim W . Integrated biochemical and computational approach identifies BCL6 direct target genes controlling multiple pathways in normal germinal center B cells. Blood. 2009; 115(5):975-84. PMC: 2817639. DOI: 10.1182/blood-2009-06-227017. View

2.
Bruford E, Lush M, Wright M, Sneddon T, Povey S, Birney E . The HGNC Database in 2008: a resource for the human genome. Nucleic Acids Res. 2007; 36(Database issue):D445-8. PMC: 2238870. DOI: 10.1093/nar/gkm881. View

3.
Margolin A, Palomero T, Sumazin P, Califano A, Ferrando A, Stolovitzky G . ChIP-on-chip significance analysis reveals large-scale binding and regulation by human transcription factor oncogenes. Proc Natl Acad Sci U S A. 2009; 106(1):244-9. PMC: 2613038. DOI: 10.1073/pnas.0806445106. View

4.
Espinosa L, Cathelin S, DAltri T, Trimarchi T, Statnikov A, Guiu J . The Notch/Hes1 pathway sustains NF-κB activation through CYLD repression in T cell leukemia. Cancer Cell. 2010; 18(3):268-81. PMC: 2963042. DOI: 10.1016/j.ccr.2010.08.006. View

5.
Kirmizis A, Farnham P . Genomic approaches that aid in the identification of transcription factor target genes. Exp Biol Med (Maywood). 2004; 229(8):705-21. DOI: 10.1177/153537020422900803. View