Ast 3D volumetric imaging method enabled acquisitions of temporal and spatial imaging of the injected pre-polarized substrate and its metabolites throughout the rat torso and abdomen. Since the relative lactate to 256373-96-3 pyruvate signals measured in the kidneys showed little difference between the treated and the control animals, it is likely that the decrease in apparent flux between pyruvate and lactate was the result of the radiation therapy to the tumors. Although DCE-MR imaging was not performed in this study, 25033180 the temporal dynamics of the substrate bolus signal in the tumor were recorded at similar time points and temporal resolution compared to DCE-MR imaging (the time from injection to the peak of the pyruvate signal in the tumors), and was found to be similar between the two groups. The total cumulative 13C signals in the tumor relative to the kidney (pyruvate+lactate from all time points) were also very similar between the two groups. Since the hyperpolarized 13C substrate was administered intravenously, a decrease in tumor perfusion would presumably result in lower overall 13C signal in the tumor. Thus the observed changes in apparent metabolic flux were likely not caused by any substantial changes in tumor perfusion, but more studies are needed to confirm this. Similar to prior studies investigating the decrease in the [1-13C]lactate in tumors following chemotherapy, the metabolic changes observed in MDA-MB-231 tumors in this study were associated with an increase in apoptosis at 96 hours after the single dose of ionizing radiation. In addition to the increase in cell apoptosis, the radiation therapy also induced a significant degree of senescence in these tumors [38,39]. The cell senescence may have contributed to the apparent increase in tumor size in the treated cohort, as senescent cells are generally much larger in size as compared to proliferating cells [38]. However, it is also possible that the slightly longer period from tumor cell implantation to imaging for the treatment group has also contributed to this difference in tumor size. The potential impact of the therapyinduced apoptosis and senescence on the flux between pyruvate and lactate measured was also investigated in vitro in the same cell line. Similar to the tumors, at 96 hours after a dose16 Gy radiation, MDA-MB-231 cells in vitro showed a small increase in apoptosis but also the majority became senescent. Since we observed a greater than 40 reduction in the apparent flux between pyruvate and lactate in tumors, while only 10 more of tumor cells become apoptotic (more than 80 of the tumor cells were still 298690-60-5 web non-apoptotic post treatment), thus, the radiationinduced cell senescence and additional cellular and tissue changes may have also contributed to the observed decrease in metabolic flux. p53 activation and downstream regulation of metabolism is observed in some tumors with ionization radiation inducedRadiation Therapy Response and 13C Metabolic MRIRadiation Therapy Response and 13C Metabolic MRIFigure 5. Western blot analysis was used to assess cell membrane monocarboxylate transport and lactate dehydrogenase levels. Tissue hypoxia in the tumors was also assessed by HIF1-a expression. A) Western blots showed a decrease in MCT4 expression in MDA-MB-231 tumors radiation treated with radiation as compared to controls. The difference was significant (* P,0.03). B) A small decrease in MCT4 expression was observed in treated MDA-MB-231 cells in vitro. C) HIF1-a expres.Ast 3D volumetric imaging method enabled acquisitions of temporal and spatial imaging of the injected pre-polarized substrate and its metabolites throughout the rat torso and abdomen. Since the relative lactate to pyruvate signals measured in the kidneys showed little difference between the treated and the control animals, it is likely that the decrease in apparent flux between pyruvate and lactate was the result of the radiation therapy to the tumors. Although DCE-MR imaging was not performed in this study, 25033180 the temporal dynamics of the substrate bolus signal in the tumor were recorded at similar time points and temporal resolution compared to DCE-MR imaging (the time from injection to the peak of the pyruvate signal in the tumors), and was found to be similar between the two groups. The total cumulative 13C signals in the tumor relative to the kidney (pyruvate+lactate from all time points) were also very similar between the two groups. Since the hyperpolarized 13C substrate was administered intravenously, a decrease in tumor perfusion would presumably result in lower overall 13C signal in the tumor. Thus the observed changes in apparent metabolic flux were likely not caused by any substantial changes in tumor perfusion, but more studies are needed to confirm this. Similar to prior studies investigating the decrease in the [1-13C]lactate in tumors following chemotherapy, the metabolic changes observed in MDA-MB-231 tumors in this study were associated with an increase in apoptosis at 96 hours after the single dose of ionizing radiation. In addition to the increase in cell apoptosis, the radiation therapy also induced a significant degree of senescence in these tumors [38,39]. The cell senescence may have contributed to the apparent increase in tumor size in the treated cohort, as senescent cells are generally much larger in size as compared to proliferating cells [38]. However, it is also possible that the slightly longer period from tumor cell implantation to imaging for the treatment group has also contributed to this difference in tumor size. The potential impact of the therapyinduced apoptosis and senescence on the flux between pyruvate and lactate measured was also investigated in vitro in the same cell line. Similar to the tumors, at 96 hours after a dose16 Gy radiation, MDA-MB-231 cells in vitro showed a small increase in apoptosis but also the majority became senescent. Since we observed a greater than 40 reduction in the apparent flux between pyruvate and lactate in tumors, while only 10 more of tumor cells become apoptotic (more than 80 of the tumor cells were still non-apoptotic post treatment), thus, the radiationinduced cell senescence and additional cellular and tissue changes may have also contributed to the observed decrease in metabolic flux. p53 activation and downstream regulation of metabolism is observed in some tumors with ionization radiation inducedRadiation Therapy Response and 13C Metabolic MRIRadiation Therapy Response and 13C Metabolic MRIFigure 5. Western blot analysis was used to assess cell membrane monocarboxylate transport and lactate dehydrogenase levels. Tissue hypoxia in the tumors was also assessed by HIF1-a expression. A) Western blots showed a decrease in MCT4 expression in MDA-MB-231 tumors radiation treated with radiation as compared to controls. The difference was significant (* P,0.03). B) A small decrease in MCT4 expression was observed in treated MDA-MB-231 cells in vitro. C) HIF1-a expres.

Ast 3D volumetric imaging method enabled acquisitions of temporal and spatial

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