Literature DB >> 19127566

Toward an "omic" physiopathology of reactive chemicals: thirty years of mass spectrometric study of the protein adducts with endogenous and xenobiotic compounds.

Federico Maria Rubino1, Marco Pitton, Daniela Di Fabio, Antonio Colombi.   

Abstract

Cancer and degenerative diseases are major causes of morbidity and death, derived from the permanent modification of key biopolymers such as DNA and regulatory proteins by usually smaller, reactive molecules, present in the environment or generated from endogenous and xenobiotic components by the body's own biochemical mechanisms (molecular adducts). In particular, protein adducts with organic electrophiles have been studied for more than 30 [see, e.g., Calleman et al., 1978] years essentially for three purposes: (a) as passive monitors of the mean level of individual exposure to specific chemicals, either endogenously present in the human body or to which the subject is exposed through food or environmental contamination; (b) as quantitative indicators of the mean extent of the individual metabolic processing which converts a non-reactive chemical substance into its toxic products able to damage DNA (en route to cancer induction through genotoxic mechanisms) or key proteins (as in the case of several drugs, pesticides or otherwise biologically active substances); (c) to relate the extent of protein modification to that of biological function impairment (such as enzyme inhibition) finally causing the specific health damage. This review describes the role that contemporary mass spectrometry-based approaches employed in the qualitative and quantitative study of protein-electrophile adducts play in the discovery of the (bio)chemical mechanisms of toxic substances and highlights the future directions of research in this field. A particular emphasis is given to the measurement of often high levels of the protein adducts of several industrial and environmental pollutants in unexposed human populations, a phenomenon which highlights the possibility that a number of small organic molecules are generated in the human organism through minor metabolic processes, the imbalance of which may be the cause of "spontaneous" cases of cancer and of other degenerative diseases of still uncharacterized etiology. With all this in mind, it is foreseen that a holistic description of cellular functions will take advantage of new analytical methods based on time-integrated metabolomic measurements of a new biological compartment, the "adductome," aimed at better understanding integrated organism response to environmental and endogenous stressors. Copyright 2009 Wiley Periodicals, Inc.

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Year:  2009        PMID: 19127566     DOI: 10.1002/mas.20207

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  53 in total

1.  Profiling Cys34 adducts of human serum albumin by fixed-step selected reaction monitoring.

Authors:  He Li; Hasmik Grigoryan; William E Funk; Sixin Samantha Lu; Sherri Rose; Evan R Williams; Stephen M Rappaport
Journal:  Mol Cell Proteomics       Date:  2010-12-30       Impact factor: 5.911

Review 2.  Molecular mechanisms underlying chemical liver injury.

Authors:  Xinsheng Gu; Jose E Manautou
Journal:  Expert Rev Mol Med       Date:  2012-02-03       Impact factor: 5.600

Review 3.  Detection of electrophile-sensitive proteins.

Authors:  Stephanie B Wall; M Ryan Smith; Karina Ricart; Fen Zhou; Praveen K Vayalil; Joo-Yeun Oh; Aimee Landar
Journal:  Biochim Biophys Acta       Date:  2013-09-08

4.  Urinary DNA adductomics - A novel approach for exposomics.

Authors:  Marcus S Cooke; Chiung-Wen Hu; Yuan-Jhe Chang; Mu-Rong Chao
Journal:  Environ Int       Date:  2018-11-02       Impact factor: 9.621

5.  An enhanced throughput method for quantification of sulfur mustard adducts to human serum albumin via isotope dilution tandem mass spectrometry.

Authors:  Tracy M Andacht; Brooke G Pantazides; Brian S Crow; Alex Fidder; Daan Noort; Jerry D Thomas; Thomas A Blake; Rudolph C Johnson
Journal:  J Anal Toxicol       Date:  2013-11-07       Impact factor: 3.367

6.  Mass spectrometric characterization of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine N-oxidized metabolites bound at Cys34 of human serum albumin.

Authors:  Lijuan Peng; Robert J Turesky
Journal:  Chem Res Toxicol       Date:  2011-10-04       Impact factor: 3.739

7.  Mass Spectrometric Characterization of Human Serum Albumin Adducts Formed with N-Oxidized Metabolites of 2-Amino-1-methylphenylimidazo[4,5-b]pyridine in Human Plasma and Hepatocytes.

Authors:  Yi Wang; Lijuan Peng; Medjda Bellamri; Sophie Langouët; Robert J Turesky
Journal:  Chem Res Toxicol       Date:  2015-04-10       Impact factor: 3.739

8.  Mapping serum albumin adducts of the food-borne carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine by data-dependent tandem mass spectrometry.

Authors:  Lijuan Peng; Surendra Dasari; David L Tabb; Robert J Turesky
Journal:  Chem Res Toxicol       Date:  2012-08-14       Impact factor: 3.739

9.  Capturing labile sulfenamide and sulfinamide serum albumin adducts of carcinogenic arylamines by chemical oxidation.

Authors:  Lijuan Peng; Robert J Turesky
Journal:  Anal Chem       Date:  2012-12-28       Impact factor: 6.986

10.  Building exposure biology centers to put the E into "G x E" interaction studies.

Authors:  Martyn T Smith; Stephen M Rappaport
Journal:  Environ Health Perspect       Date:  2009-08       Impact factor: 9.031

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