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Oral perfluorooctane sulfonate (PFOS) lessens tumor development in the APC(min) mouse model of spontaneous familial adenomatous polyposis

Wimsatt, Jeffrey (author)
Department of Medicine, School of Medicine, West Virginia University, Morgantown, USA; Department of Epidemiology, School of Public Health, West Virginia University, Morgantown, USA; West Virginia University, Morgantown, USA
Villers, Meghan (author)
Department of Medicine, School of Medicine, West Virginia University, Morgantown, USA
Thomas, Laurel (author)
Department of Medicine, School of Medicine, West Virginia University, Morgantown, USA
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Kamarec, Stacey (author)
Department of Medicine, School of Medicine, West Virginia University, Morgantown, USA
Montgomery, Caitlin (author)
Department of Medicine, School of Medicine, West Virginia University, Morgantown, USA
Yeung, Leo W. Y., 1981- (author)
Örebro universitet,Institutionen för naturvetenskap och teknik,Man-Technology-Environment (MTM) Research Centre
Hu, Yanqing (author)
Department of Statistics, West Virginia University, Morgantown, USA
Innes, Kim (author)
Department of Epidemiology, School of Public Health, West Virginia University, Morgantown, USA
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 (creator_code:org_t)
2016-12-08
2016
English.
In: BMC Cancer. - London, United Kingdom : BioMed Central. - 1471-2407. ; 16:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Colorectal cancer is the second most common cause of cancer deaths for both men and women, and the third most common cause of cancer in the U.S. Toxicity of current chemotherapeutic agents for colorectal cancer, and emergence of drug resistance underscore the need to develop new, potentially less toxic alternatives. Our recent cross-sectional study in a large Appalachian population, showed a strong, inverse, dose-response association of serum perfluorooctane sulfonate (PFOS) levels to prevalent colorectal cancer, suggesting PFOS may have therapeutic potential in the prevention and/or treatment of colorectal cancer. In these preliminary studies using a mouse model of familial colorectal cancer, the APC(min) mouse, and exposures comparable to those reported in human populations, we assess the efficacy of PFOS for reducing tumor burden, and evaluate potential dose-response effects.Methods: At 5-6 weeks of age, APC(min) mice were randomized to receive 0, 20, 250 mg PFOS/kg (females) or 0, 10, 50 and 200 mg PFOS/kg (males) via their drinking water. At 15 weeks of age, gastrointestinal tumors were counted and scored and blood PFOS levels measured.Results: PFOS exposure was associated with a significant, dose-response reduction in total tumor number in both male and female mice. This inverse dose-response effect of PFOS exposure was particularly pronounced for larger tumors (r(2) for linear trend = 0.44 for males, p's <0.001).Conclusions: The current study in a mouse model of familial adenomatous polyposis offers the first experimental evidence that chronic exposure to PFOS in drinking water can reduce formation of gastrointestinal tumors, and that these reductions are both significant and dose-dependent. If confirmed in further studies, these promising findings could lead to new therapeutic strategies for familial colorectal cancer, and suggest that PFOS testing in both preventive and therapeutic models for human colorectal cancer is warranted.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

APCmin mouse
Perfluorooctane sulfonate
PFOS
Colorectal cancer
Dose–response
Gender
Onkologi
Oncology

Publication and Content Type

ref (subject category)
art (subject category)

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