posted on 2020-04-13, 19:23authored byMark Woollam, Meghana Teli, Shengzhi Liu, Ali Daneshkhah, Amanda P. Siegel, Hiroki Yokota, Mangilal Agarwal
Urinary
volatile terpene (VT) levels are significantly altered
with induced models of breast cancer in mice. The question arises
whether VTs can detect the efficacy of antitumor treatments. BALB/c
mice were injected with 4T1.2 murine tumor cells in the mammary pad
or iliac artery to model localized breast cancer and induced bone
metastasis. The effect of two dopaminergic antitumor agents was tested
by conventional histology and altered VT levels. The headspace of
urine specimens was analyzed by gas chromatography–mass spectrometry.
In the localized model, the statistical significance (p < 0.05) was identified for 26% of VTs, and in the metastasis
model, 19% of VTs. The authors discovered separate VT panels classifying
localized/control [area under the curve (AUC) = 1.0] and metastasis/control
(AUC = 0.98). Treatment samples were tested using these panels, which
showed that mice treated with either agent were statistically significantly
different from cancer samples, which is consistent with conventional
analysis.