Effects of folate deficiency and sex on carcinogenesis in a mouse model of oral cancer

Author:

Pitstick Lenore1,Goral Joanna2ORCID,Ciancio Mae J.3,Meyer Alice2,Pytynia Matthew3,Bychek Sofia3,Zidan Safia3,Shuey Jennifer4,Jham Bruno C.5ORCID,Green Jacalyn M.1ORCID

Affiliation:

1. Department of Biochemistry and Molecular Genetics, College of Graduate Studies Midwestern University Downers Grove Illinois USA

2. Department of Anatomy, College of Graduate Studies Midwestern University Downers Grove Illinois USA

3. Biomedical Sciences Program, College of Graduate Studies Midwestern University Downers Grove Illinois USA

4. Chicago College of Osteopathic Medicine Midwestern University Downers Grove Illinois USA

5. College of Dental Medicine‐Illinois Midwestern University Downers Grove Illinois USA

Abstract

AbstractObjectivesTo investigate the effects of dietary folate and sex on histopathology of oral squamous cell carcinoma in mice.Materials and MethodsMice (C57Bl/6, 30/sex) were fed either a deficient folate or sufficient folate diet. Vehicle or 4‐nitroquinoline1‐oxide (50 μg/mL) in vehicle were administered in drinking water for 20 weeks, followed by 6 weeks of regular drinking water. Oral lesions were observed weekly. Tongues were studied for histopathologic changes. Immunohistochemical techniques were used to measure cell proliferation (Ki67+), and to quantify expression of folate receptor, reduced folate carrier, and proton‐coupled folate transporter. T cells, macrophages, and neutrophils were counted and normalized to area.ResultsAll 4NQO‐treated mice developed oral tumors. Dietary folate level did not affect tumor burden. More tumors were observed on the ventral aspect of the tongue than in other locations within the oral cavity. 4‐nitroquinoline‐1‐oxide‐treated mice displayed 27%–46% significantly lower expression of all three folate transport proteins; diet and sex had no effect on folate transporter expression. T‐cell and neutrophil infiltration in tongues were 9.1‐fold and 18.1‐fold increased in the 4‐nitroquinoline‐1‐oxide‐treated mouse tongues than in controls.ConclusionTreatment with 4NQO was the primary factor in determining cancer development, decreased folate transport expression, and lymphoid cell infiltration.

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Reference82 articles.

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2. Succinylsulfathiazole modulates the mTOR signaling pathway in the liver of c57BL/6 mice via a folate independent mechanism

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