Literature DB >> 10628055

Pathological excretion patterns of urinary proteins in renal cell cancer patients exposed to trichloroethylene.

T Brüning1, H Mann, H Melzer, A G Sundberg, H M Bolt.   

Abstract

A study was carried out to investigate urinary protein excretion patterns by means of SDS-polyacrylamide-gel-electrophoresis (SDS-PAGE) in renal cell cancer patients who had previously been exposed to high levels of trichloroethylene. Thirty-eight out of 41 (93%) renal cell cancer patients investigated had former extensive trichloroethylene exposure, but only 23 out of 50 (46%) renal cell cancer patients without a history of occupational exposure to trichloroethylene revealed urinary protein patterns indicative of toxic effects on the tubular system. One hundred controls without histories of overt renal disease and not occupationally exposed to trichloroethylene were examined in the same way; only 11 (11%) of them displayed protein excretion patterns indicative of damage to the renal tubule. These results are supported by alpha 1-microglobulin excretion data. The following conclusions are drawn: (1) Substantially more cases of tubular damage are found amongst renal cell carcinoma patients having been exposed to substantial levels of trichloroethylene over many years as compared with renal cell carcinoma patients not exposed to trichloroethylene. (2) The results support the view that chronic tubular damage is a precondition for the nephrocarcinogenic effect of trichloroethylene. (3) The findings indicate that urine protein patterns, on the basis of the SDS-PAGE methodology, represent a 'biological effect parameter' for the medical surveillance of persons occupationally exposed to trichloroethylene.

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Year:  1999        PMID: 10628055     DOI: 10.1093/occmed/49.5.299

Source DB:  PubMed          Journal:  Occup Med (Lond)        ISSN: 0962-7480            Impact factor:   1.611


  8 in total

1.  Elevated urinary levels of kidney injury molecule-1 among Chinese factory workers exposed to trichloroethylene.

Authors:  Roel Vermeulen; Luoping Zhang; Annejet Spierenburg; Xiaojian Tang; Joseph V Bonventre; Boris Reiss; Min Shen; Martyn T Smith; Chuangyi Qiu; Yichen Ge; Zhiying Ji; Jun Xiong; Jian He; Zhenyue Hao; Songwang Liu; Yuxuan Xie; Fei Yue; Weihong Guo; Mark Purdue; Laura E Beane Freeman; Venkata Sabbisetti; Laiyu Li; Hanlin Huang; Nathaniel Rothman; Qing Lan
Journal:  Carcinogenesis       Date:  2012-06-04       Impact factor: 4.944

2.  Mutagenicity of the cysteine S-conjugate sulfoxides of trichloroethylene and tetrachloroethylene in the Ames test.

Authors:  Roy M Irving; Adnan A Elfarra
Journal:  Toxicology       Date:  2013-02-13       Impact factor: 4.221

Review 3.  Role of reactive metabolites in the circulation in extrahepatic toxicity.

Authors:  Roy M Irving; Adnan A Elfarra
Journal:  Expert Opin Drug Metab Toxicol       Date:  2012-06-11       Impact factor: 4.481

4.  Characterization of the chemical reactivity and nephrotoxicity of N-acetyl-S-(1,2-dichlorovinyl)-L-cysteine sulfoxide, a potential reactive metabolite of trichloroethylene.

Authors:  Roy M Irving; Marie E Pinkerton; Adnan A Elfarra
Journal:  Toxicol Appl Pharmacol       Date:  2012-12-16       Impact factor: 4.219

Review 5.  Target Organ Metabolism, Toxicity, and Mechanisms of Trichloroethylene and Perchloroethylene: Key Similarities, Differences, and Data Gaps.

Authors:  Joseph A Cichocki; Kathryn Z Guyton; Neela Guha; Weihsueh A Chiu; Ivan Rusyn; Lawrence H Lash
Journal:  J Pharmacol Exp Ther       Date:  2016-08-10       Impact factor: 4.030

Review 6.  Trichloroethylene: Mechanistic, epidemiologic and other supporting evidence of carcinogenic hazard.

Authors:  Ivan Rusyn; Weihsueh A Chiu; Lawrence H Lash; Hans Kromhout; Johnni Hansen; Kathryn Z Guyton
Journal:  Pharmacol Ther       Date:  2013-08-23       Impact factor: 12.310

7.  Urinary alpha1-microglobulin excretion as biomarker of renal toxicity in trichloroethylene-exposed persons.

Authors:  Hermann M Bolt; Magda Lammert; Silvia Selinski; Thomas Brüning
Journal:  Int Arch Occup Environ Health       Date:  2004-02-25       Impact factor: 3.015

8.  Combined GSTM1-Null, GSTT1-Active, GSTA1 Low-Activity and GSTP1-Variant Genotype Is Associated with Increased Risk of Clear Cell Renal Cell Carcinoma.

Authors:  Vesna M Coric; Tatjana P Simic; Tatjana D Pekmezovic; Gordana M Basta-Jovanovic; Ana R Savic Radojevic; Sanja M Radojevic-Skodric; Marija G Matic; Dejan P Dragicevic; Tanja M Radic; Ljiljana M Bogdanovic; Zoran M Dzamic; Marija S Pljesa-Ercegovac
Journal:  PLoS One       Date:  2016-08-08       Impact factor: 3.240

  8 in total

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