Literature DB >> 9512930

Molecular profiling of non-genotoxic hepatocarcinogenesis using differential display reverse transcription-polymerase chain reaction (ddRT-PCR).

J C Rockett1, D J Esdaile, G G Gibson.   

Abstract

The technique of differential display reverse transcription-polymerase chain reaction (ddRT-PCR) has been used to produce unique profiles of up-regulated and down-regulated gene expression in the liver of male Wistar rats following short term exposure to the non-genotoxic hepatocarcinogens, phenobarbital and WY-14,643. Animals were treated for 3 days, whereupon their livers were extracted and snap frozen. mRNA was prepared from the livers and used for ddRT-PCR. Individual bands from the differential displays were extracted and cloned. False positives were eliminated by dotblot screening and true positives then sequenced and identified.

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Year:  1997        PMID: 9512930     DOI: 10.1007/BF03190966

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  5 in total

Review 1.  Prediction of non-genotoxic carcinogenesis.

Authors:  J Ashby
Journal:  Toxicol Lett       Date:  1992-12       Impact factor: 4.372

2.  Rapid determination of the complexity of cDNA bands extracted from DDRT-PCR polyacrylamide gels.

Authors:  N R Smith; A Li; M Aldersley; A S High; A F Markham; P A Robinson
Journal:  Nucleic Acids Res       Date:  1997-09-01       Impact factor: 16.971

Review 3.  Role of persistent, non-genotoxic tissue damage in rodent cancer and relevance to humans.

Authors:  P Grasso; M Sharratt; A J Cohen
Journal:  Annu Rev Pharmacol Toxicol       Date:  1991       Impact factor: 13.820

Review 4.  Mechanisms of hepatocarcinogenicity of peroxisome-proliferating drugs and chemicals.

Authors:  B G Lake
Journal:  Annu Rev Pharmacol Toxicol       Date:  1995       Impact factor: 13.820

Review 5.  Non-genotoxic factors in the carcinogenetic process: problems of detection and hazard evaluation.

Authors:  S Parodi; D Malacarne; M Taningher
Journal:  Toxicol Lett       Date:  1992-12       Impact factor: 4.372

  5 in total

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