## Abstract ## Purpose To study the impact of Gd‐DTPA‐BMA on choline signals of HT29 colon carcinomas determined by localized ^1^H MRS in vivo at 4.7T. ## Materials and Methods PRESS ^1^H MR spectra (2‐second repetition time and echo times of 20–272 msec) were acquired from HT29 xenografts prior
Detection of apoptotic cell death in vitro in the presence of Gd-DTPA-BMA
✍ Scribed by Colleen Bailey; Anoja Giles; Gregory J. Czarnota; Greg J. Stanisz
- Book ID
- 102953097
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 861 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Due to variability in patient response to cancer therapy, there is a growing interest in monitoring patient progress during treatment. Apoptotic cell death is one early marker of tumor response to treatment. Using known extracellular concentrations of gadolinium diethylenetriamine pentaacetic acid bismethylamide (Gd‐DTPA‐BMA) to vary the exchange regime, T~1~ and T~2~ relaxation data for acute myeloid leukemia (AML) cell samples were obtained and then analyzed using a two‐pool model of relaxation with exchange. Leukemia cells treated with cisplatin to induce apoptosis exhibited a statistically significant (P < 0.05) decrease in intracellular longitudinal relaxation time, T~1I~, from 1030 ms to 940 ms, a decrease (P < 0.001) in the intracellular water fraction, M~0I~, from 0.86 to 0.68 and a statistically significant increase (P < 0.01) in transmembrane water exchange rate, k~IE~, from 1.4 s^−1^ to 6.8 s^−1^. The changes in MR parameters correlated with quantitative histology, such as cellular cross‐sectional area and average nuclear area measurements. The results of this study emphasize the importance of accounting for water exchange in dynamic contrast‐enhanced MRI (DCE‐MRI) studies, particularly those that examine tumor response to therapies in which apoptotic changes occur. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
We developed an in vitro model to study the effect of anti-recoverin antibodies on retinal cells and the mechanism(s) by which they kill photoreceptors in cancer-associated retinopathy (CAR). Rat retinal cells were grown in a defined medium, and cell types were identified by using antibodies against
Magnetization transfer (MT) and T(1) and T(2) relaxation of normal, trypsinized, and interleukin-1beta (IL-1beta)-treated cartilage were measured in the absence and presence of Gd-DTPA(2-). Without the addition of Gd-DTPA(2-), neither T(1) nor T(2) showed any significant change with cartilage damage
## Abstract MRI‐based cartilage morphometry can monitor cartilage loss in osteoarthritis. Intravenous Gd‐DTPA injection is needed for compositional (proteoglycan) cartilage imaging with delayed gadolinium enhanced MRI (dGEMRIC). However, longitudinal changes of cartilage morphology have not been co