Literature DB >> 23339022

Cellular-signaling pathways unveil the carcinogenic potential of chemicals.

Giel Hendriks1, Bob van de Water, Willem Schoonen, Harry Vrieling.   

Abstract

Most of the current in vitro carcinogenicity assays assess the potential carcinogenic properties of chemicals through the detection of inflicted DNA damage or subsequent chromosome damage and gene mutations. Unfortunately, these assays generally do not provide mechanistic insight into the reactive properties of a chemical. Upon chemical-induced damage of biomolecules, molecular sensors will activate general and damage-specific cellular response pathways that provide protection against the (geno)toxic and potential carcinogenic properties of chemicals. These cellular defense mechanisms include activation of cell-cycle checkpoints, DNA repair systems and induction of apoptosis or necrosis. Visualization of activated cellular-signaling pathways forms a powerful means to readily detect the genotoxic potential of chemical compounds and simultaneously gain insight into their reactive properties. Over the past years, various in vitro reporter assays have been developed that monitor activation of general and more specific cellular-signaling pathways, including the GreenScreen HC and ToxTracker assays. In this review we provide a perspective on how we can exploit activation of cellular signaling pathways to shed light on the mode of action of the chemical exposure and to develop sophisticated mechanism-based in vitro assays for cancer risk assessment.
Copyright © 2013 John Wiley & Sons, Ltd.

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Year:  2013        PMID: 23339022     DOI: 10.1002/jat.2845

Source DB:  PubMed          Journal:  J Appl Toxicol        ISSN: 0260-437X            Impact factor:   3.446


  7 in total

1.  The Extended ToxTracker Assay Discriminates Between Induction of DNA Damage, Oxidative Stress, and Protein Misfolding.

Authors:  Giel Hendriks; Remco S Derr; Branislav Misovic; Bruno Morolli; Fabienne M G R Calléja; Harry Vrieling
Journal:  Toxicol Sci       Date:  2015-12-29       Impact factor: 4.849

Review 2.  Cell-Based Assay Design for High-Content Screening of Drug Candidates.

Authors:  Gregory Nierode; Paul S Kwon; Jonathan S Dordick; Seok-Joon Kwon
Journal:  J Microbiol Biotechnol       Date:  2016-02       Impact factor: 2.351

3.  Identification of genotoxic compounds using isogenic DNA repair deficient DT40 cell lines on a quantitative high throughput screening platform.

Authors:  Kana Nishihara; Ruili Huang; Jinghua Zhao; Sampada A Shahane; Kristine L Witt; Stephanie L Smith-Roe; Raymond R Tice; Shunichi Takeda; Menghang Xia
Journal:  Mutagenesis       Date:  2015-08-04       Impact factor: 3.000

4.  Comparison of the metabolic activation of environmental carcinogens in mouse embryonic stem cells and mouse embryonic fibroblasts.

Authors:  Annette M Krais; Karl-Rudolf Mühlbauer; Jill E Kucab; Helena Chinbuah; Michael G Cornelius; Quan-Xiang Wei; Monica Hollstein; David H Phillips; Volker M Arlt; Heinz H Schmeiser
Journal:  Toxicol In Vitro       Date:  2014-09-16       Impact factor: 3.500

5.  Mechanism of aromatic amine carcinogen bypass by the Y-family polymerase, Dpo4.

Authors:  Alfonso Brenlla; David Rueda; Louis J Romano
Journal:  Nucleic Acids Res       Date:  2015-10-19       Impact factor: 16.971

6.  Understanding the role of potential pathways and its components including hypoxia and immune system in case of oral cancer.

Authors:  Leena Hussein Bajrai; Sayed Sartaj Sohrab; Mohammad Mobashir; Mohammad Amjad Kamal; Moshahid Alam Rizvi; Esam Ibraheem Azhar
Journal:  Sci Rep       Date:  2021-10-01       Impact factor: 4.379

7.  Mechanism-based genotoxicity screening of metal oxide nanoparticles using the ToxTracker panel of reporter cell lines.

Authors:  Hanna L Karlsson; Anda R Gliga; Fabienne M G R Calléja; Cátia S A G Gonçalves; Inger Odnevall Wallinder; Harry Vrieling; Bengt Fadeel; Giel Hendriks
Journal:  Part Fibre Toxicol       Date:  2014-09-02       Impact factor: 9.400

  7 in total

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