Literature DB >> 18055024

Connecting chemosensitivity, gene expression and disease.

David G Covell1.   

Abstract

Omics-based investigations offer potentially powerful readouts that might be useful for probing the underlying biology of normal and diseased states, identifying novel therapeutic targets and proposing relevant markers for designing treatment strategies. A vital component of these investigations involves a systematic analysis of gene expression and chemosensitivity data in the context of disease states and small molecule probes into the function of targets responsible for a disease phenotype. Systematic analysis of chemical and pharmacogenetics data offers a possible means to identify novel, small-molecule, potentially therapeutic, agents that affect the phenotype of a particular target. Elegantly simple in concept, the covariation of genetic and chemosensitivity readouts provide a hypothetical link for relating compounds through genomic expression profiles to underlying biology.

Mesh:

Year:  2007        PMID: 18055024     DOI: 10.1016/j.tips.2007.10.015

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  3 in total

1.  Predictive value of MTT assay as an in vitro chemosensitivity testing for gastric cancer: one institution's experience.

Authors:  Bin Wu; Jin-Shui Zhu; Yi Zhang; Wei-Ming Shen; Qiang Zhang
Journal:  World J Gastroenterol       Date:  2008-05-21       Impact factor: 5.742

Review 2.  Asparagine synthetase: a new potential biomarker in ovarian cancer.

Authors:  Philip L Lorenzi; John N Weinstein
Journal:  Drug News Perspect       Date:  2009 Jan-Feb

Review 3.  Using drug response data to identify molecular effectors, and molecular "omic" data to identify candidate drugs in cancer.

Authors:  William C Reinhold; Sudhir Varma; Vinodh N Rajapakse; Augustin Luna; Fabricio Garmus Sousa; Kurt W Kohn; Yves G Pommier
Journal:  Hum Genet       Date:  2014-09-12       Impact factor: 4.132

  3 in total

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