| Literature DB >> 26880804 |
John A Cook1, Gadisetti V R Chandramouli1, Miriam R Anver2, Anastasia L Sowers1, Angela Thetford1, Kristopher W Krausz3, Frank J Gonzalez3, James B Mitchell4, Andrew D Patterson5.
Abstract
Nonlethal exposure to ionizing radiation (IR) is a public concern due to its known carcinogenic effects. Although latency periods for IR-induced neoplasms are relatively long, the ability to detect cancer as early as possible is highly advantageous for effective therapeutic intervention. Therefore, we hypothesized that metabolites in the urine from mice exposed to total body radiation (TBI) would predict for the presence of cancer before a palpable mass was detected. In this study, we exposed mice to 0 or 5.4 Gy TBI, collected urine samples periodically over 1 year, and assayed urine metabolites by using mass spectrometry. Longitudinal data analysis within the first year post-TBI revealed that cancers, including hematopoietic, solid, and benign neoplasms, could be distinguished by unique urinary signatures as early as 3 months post-TBI. Furthermore, a distinction among different types of malignancies could be clearly delineated as early as 3 months post-TBI for hematopoietic neoplasms, 6 months for solid neoplasms, and by 1 year for benign neoplasms. Moreover, the feature profile for radiation-exposed mice 6 months post-TBI was found to be similar to nonirradiated control mice at 18 months, suggesting that TBI accelerates aging. These results demonstrate that urine feature profiles following TBI can identify cancers in mice prior to macroscopic detection, with important implications for the early diagnosis and treatment. ©2016 American Association for Cancer Research.Entities:
Mesh:
Year: 2016 PMID: 26880804 PMCID: PMC4794383 DOI: 10.1158/0008-5472.CAN-15-2416
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701