Literature DB >> 16806863

Pulmonary tumor types induced in Wistar rats of the so-called "19-dust study".

Ulrich Mohr1, Heinrich Ernst, Markus Roller, Friedrich Pott.   

Abstract

The incidences of primary lung tumor types histologically diagnosed in 28 groups of Wistar rats of the so-called "19-dust study" are described, the total study having been already presented by Pott and Roller (Carcinogenicity study with nineteen granular dusts in rats. Eur J Oncol, 2005; 10: 249-81). Each exposed group was repeatedly instilled intratracheally with a suspension of one type and dose of 13 non-mining dusts differing in at least one of the following properties: chemical composition, density, specific surface area, and mean particle size. Eleven of the 13 dusts were classified as respirable granular bio-durable particles without known significant specific toxicity (abbreviation of the nine-word definition: GBP). In 579 (58%) lungs of 1002 rats which survived more than 26 weeks after the first instillation of GBP, at least one primary lung tumor type was observed, and in 306 (31%) at least two types. Three benign tumor types were diagnosed in the 579 tumor-bearing rats: bronchiolo-alveolar adenoma in 46%, cystic keratinizing epithelioma in 53%, and non-keratinizing epithelioma in 2.6% of the rats. Two of three malignant tumor types (bronchiolo-alveolar carcinoma and squamous cell carcinoma) occurred in 46% and 31% of the tumor-bearing rats, respectively, and adenosquamous carcinoma was diagnosed in 0.9%. Numerous lungs with a malignant tumor also showed one or more benign tumor types. In addition, single or multiple metastases from primary tumors of other sites (mainly carcinoma of the uterus) were diagnosed in 14% of the 1002 lungs. The proportionate incidences of the four predominantly diagnosed tumor types were compared with three summarized experimental groups which were exposed either to carbon black (two size classes), to titanium dioxide (two size classes), or to the total of the other nine GBP. A significant difference was not detected. The combination of dust volume with particle size correlated best with the carcinogenic effect, in contrast to dust mass and surface area.

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Year:  2006        PMID: 16806863     DOI: 10.1016/j.etp.2006.06.001

Source DB:  PubMed          Journal:  Exp Toxicol Pathol        ISSN: 0940-2993


  16 in total

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2.  Pulmonary exposure to carbon black by inhalation or instillation in pregnant mice: effects on liver DNA strand breaks in dams and offspring.

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Journal:  Carcinogenesis       Date:  2015-06       Impact factor: 4.944

4.  Small airway epithelial cells exposure to printer-emitted engineered nanoparticles induces cellular effects on human microvascular endothelial cells in an alveolar-capillary co-culture model.

Authors:  Jennifer D Sisler; Sandra V Pirela; Sherri Friend; Mariana Farcas; Diane Schwegler-Berry; Anna Shvedova; Vincent Castranova; Philip Demokritou; Yong Qian
Journal:  Nanotoxicology       Date:  2014-11-11       Impact factor: 5.913

5.  Summary of chemically induced pulmonary lesions in the National Toxicology Program (NTP) toxicology and carcinogenesis studies.

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Journal:  Toxicol Pathol       Date:  2008-04-25       Impact factor: 1.902

6.  Effects of copy center particles on the lungs: a toxicological characterization using a Balb/c mouse model.

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7.  Relationship of pulmonary toxicity and carcinogenicity of fine and ultrafine granular dusts in a rat bioassay.

Authors:  Angelika Kolling; Heinrich Ernst; Susanne Rittinghausen; Uwe Heinrich
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8.  An intratracheal instillation bioassay system for detection of lung toxicity due to fine particles in f344 rats.

Authors:  Masanao Yokohira; Toshiya Kuno; Keiko Yamakawa; Nozomi Hashimoto; Fumiko Ninomiya; Satoshi Suzuki; Kousuke Saoo; Katsumi Imaida
Journal:  J Toxicol Pathol       Date:  2009-04-06       Impact factor: 1.628

9.  Characterisation of the proximal airway squamous metaplasia induced by chronic tobacco smoke exposure in spontaneously hypertensive rats.

Authors:  Sarah J Bolton; Kate Pinnion; Victor Oreffo; Martyn Foster; Kent E Pinkerton
Journal:  Respir Res       Date:  2009-11-24

10.  Long-Term Exposure to Nanosized TiO2 Triggers Stress Responses and Cell Death Pathways in Pulmonary Epithelial Cells.

Authors:  Mayes Alswady-Hoff; Johanna Samulin Erdem; Santosh Phuyal; Oskar Knittelfelder; Animesh Sharma; Davi de Miranda Fonseca; Øivind Skare; Geir Slupphaug; Shanbeh Zienolddiny
Journal:  Int J Mol Sci       Date:  2021-05-19       Impact factor: 5.923

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