Literature DB >> 34228183

GFP-fused yeast cells as whole-cell biosensors for genotoxicity evaluation of nitrosamines.

Ying He1,2, Haotian Ding1,2, Xingya Xia1,2, Wenyi Qi1,2, Huaisong Wang1, Wenyuan Liu3, Feng Zheng4,5.   

Abstract

Nitrosamine compounds, represented by N-nitrosodimethylamine, are regarded as potentially genotoxic impurities (PGIs) due to their hazard warning structure, which has attracted great attention of pharmaceutical companies and regulatory authorities. At present, great research gaps exist in genotoxicity assessment and carcinogenicity comparison of nitrosamine compounds. In this work, a collection of GFP-fused yeast cells representing DNA damage repair pathways were used to evaluate the genotoxicity of eight nitrosamine compounds (10-6-105 μg/mL). The high-resolution expression profiles of GFP-fused protein revealed the details of the DNA damage repair of nitrosamines. Studies have shown that nitrosamine compounds can cause extensive DNA damage and activate multiple repair pathways. The evaluation criteria based on the total expression level of protein show a good correlation with the mammalian carcinogenicity data TD50, and the yeast cell collection can be used as a potential reliable criterion for evaluating the carcinogenicity of compounds. The assay based on DNA damage pathway integration has high sensitivity and can be used as a supplementary method for the evaluation of trace PGIs in actual production. KEY POINTS: • The genotoxicity mechanism of nitrosamines was systematically studied. • The influence of compound structure on the efficacy of genotoxicity was explored. • GFP-fused yeast cells have the potential to evaluate impurities in production.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Carcinogenicity; DNA damage repair; Genotoxicity; Nitrosamine compounds; Substituent

Mesh:

Substances:

Year:  2021        PMID: 34228183     DOI: 10.1007/s00253-021-11426-4

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  38 in total

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Journal:  Mutat Res       Date:  1975-12       Impact factor: 2.433

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Authors:  Daniel Ballmaier; Bernd Epe
Journal:  Toxicology       Date:  2006-02-21       Impact factor: 4.221

6.  Carcinogens are mutagens: a simple test system combining liver homogenates for activation and bacteria for detection.

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Journal:  Proc Natl Acad Sci U S A       Date:  1973-08       Impact factor: 11.205

7.  Protective effect of vitamin C towards N-nitrosamine-induced DNA damage in the single-cell gel electrophoresis (SCGE)/HepG2 assay.

Authors:  Nuria Arranz; Ana I Haza; Almudena García; Joseph Rafter; Paloma Morales
Journal:  Toxicol In Vitro       Date:  2007-04-14       Impact factor: 3.500

8.  Prediction and classification of the modes of genotoxic actions using bacterial biosensors specific for DNA damages.

Authors:  Joo-Myung Ahn; Ee Taek Hwang; Chul-Hee Youn; Danusia L Banu; Byoung Chan Kim; Javed H Niazi; Man Bock Gu
Journal:  Biosens Bioelectron       Date:  2009-08-25       Impact factor: 10.618

9.  Current and future application of genetic toxicity assays: the role and value of in vitro mammalian assays.

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  1 in total

1.  Trace Level Quantification of 4-Methyl-1-nitrosopiperazin in Rifampicin Capsules by LC-MS/MS.

Authors:  Xiaosha Tao; Ye Tian; Wan-Hui Liu; Shangchen Yao; Lihui Yin
Journal:  Front Chem       Date:  2022-02-14       Impact factor: 5.221

  1 in total

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