Cargando…

Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis

BACKGROUND: The biomedical literature is a rich source of associative information but too vast for complete manual review. We have developed an automated method of literature interrogation called "Literature Lab" that identifies and ranks associations existing in the literature between gen...

Descripción completa

Detalles Bibliográficos
Autores principales: Febbo, Phillip G, Mulligan, Mike G, Slonina, David A, Stegmeir, Kimberly, Di Vizio, Dolores, Martinez, Paul R, Loda, Massimo, Taylor, Stephen C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244637/
https://www.ncbi.nlm.nih.gov/pubmed/18088408
http://dx.doi.org/10.1186/1471-2164-8-461
_version_ 1782150649277841408
author Febbo, Phillip G
Mulligan, Mike G
Slonina, David A
Stegmeir, Kimberly
Di Vizio, Dolores
Martinez, Paul R
Loda, Massimo
Taylor, Stephen C
author_facet Febbo, Phillip G
Mulligan, Mike G
Slonina, David A
Stegmeir, Kimberly
Di Vizio, Dolores
Martinez, Paul R
Loda, Massimo
Taylor, Stephen C
author_sort Febbo, Phillip G
collection PubMed
description BACKGROUND: The biomedical literature is a rich source of associative information but too vast for complete manual review. We have developed an automated method of literature interrogation called "Literature Lab" that identifies and ranks associations existing in the literature between gene sets, such as those derived from microarray experiments, and curated sets of key terms (i.e. pathway names, medical subject heading (MeSH) terms, etc). RESULTS: Literature Lab was developed using differentially expressed gene sets from three previously published cancer experiments and tested on a fourth, novel gene set. When applied to the genesets from the published data including an in vitro experiment, an in vivo mouse experiment, and an experiment with human tumor samples, Literature Lab correctly identified known biological processes occurring within each experiment. When applied to a novel set of genes differentially expressed between locally invasive and metastatic prostate cancer, Literature Lab identified a strong association between the pathway term "FOSB" and genes with increased expression in metastatic prostate cancer. Immunohistochemistry subsequently confirmed increased nuclear FOSB staining in metastatic compared to locally invasive prostate cancers. CONCLUSION: This work demonstrates that Literature Lab can discover key biological processes by identifying meritorious associations between experimentally derived gene sets and key terms within the biomedical literature.
format Text
id pubmed-2244637
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-22446372008-02-15 Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis Febbo, Phillip G Mulligan, Mike G Slonina, David A Stegmeir, Kimberly Di Vizio, Dolores Martinez, Paul R Loda, Massimo Taylor, Stephen C BMC Genomics Software BACKGROUND: The biomedical literature is a rich source of associative information but too vast for complete manual review. We have developed an automated method of literature interrogation called "Literature Lab" that identifies and ranks associations existing in the literature between gene sets, such as those derived from microarray experiments, and curated sets of key terms (i.e. pathway names, medical subject heading (MeSH) terms, etc). RESULTS: Literature Lab was developed using differentially expressed gene sets from three previously published cancer experiments and tested on a fourth, novel gene set. When applied to the genesets from the published data including an in vitro experiment, an in vivo mouse experiment, and an experiment with human tumor samples, Literature Lab correctly identified known biological processes occurring within each experiment. When applied to a novel set of genes differentially expressed between locally invasive and metastatic prostate cancer, Literature Lab identified a strong association between the pathway term "FOSB" and genes with increased expression in metastatic prostate cancer. Immunohistochemistry subsequently confirmed increased nuclear FOSB staining in metastatic compared to locally invasive prostate cancers. CONCLUSION: This work demonstrates that Literature Lab can discover key biological processes by identifying meritorious associations between experimentally derived gene sets and key terms within the biomedical literature. BioMed Central 2007-12-18 /pmc/articles/PMC2244637/ /pubmed/18088408 http://dx.doi.org/10.1186/1471-2164-8-461 Text en Copyright © 2007 Febbo et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software
Febbo, Phillip G
Mulligan, Mike G
Slonina, David A
Stegmeir, Kimberly
Di Vizio, Dolores
Martinez, Paul R
Loda, Massimo
Taylor, Stephen C
Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
title Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
title_full Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
title_fullStr Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
title_full_unstemmed Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
title_short Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
title_sort literature lab: a method of automated literature interrogation to infer biology from microarray analysis
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244637/
https://www.ncbi.nlm.nih.gov/pubmed/18088408
http://dx.doi.org/10.1186/1471-2164-8-461
work_keys_str_mv AT febbophillipg literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT mulliganmikeg literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT sloninadavida literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT stegmeirkimberly literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT diviziodolores literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT martinezpaulr literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT lodamassimo literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis
AT taylorstephenc literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis