In Vitro MRS of Cells Treated with Trastuzumab at 1.5 Tesla.

Autor: Guz, Wiesław, Podgórski, Rafal, Bober, Zuzanna, Aebisher, David, Truszkiewicz, Adrian, Olek, Marcin, Machorowska Pieniążek, Agnieszka, Kawczyk-Krupka, Aleksandra, Bartusik-Aebisher, Dorota
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Zdroj: International Journal of Molecular Sciences; Feb2024, Vol. 25 Issue 3, p1719, 21p
Abstrakt: The aim of the study was to investigate the effect of Trastuzumab on the MCF-7 and CRL-2314 breast cancer cell lines. Additionally, an attempt was made to optimize magnetic resonance spectroscopy (MRS) for cell culture studies, with particular emphasis on the impact of treatment with Trastuzumab. The research materials included MCF-7 and CRL-2314 breast cancer cell lines. The study examined the response of these cell lines to treatment with Trastuzumab. The clinical magnetic resonance imaging (MRI) system, OPTIMA MR360 manufactured by GEMS, with a magnetic field induction of 1.5 T, was used. Due to the nature of the tested objects, their size and shape, it was necessary to design and manufacture additional receiving coils. They were used to image the tested cell cultures and record the spectroscopic signal. The spectra obtained by MRS were confirmed by NMR using a 300 MHz NMR Fourier 300 with the TopSpin 3.1 system from Bruker. The designed receiving coils allowed for conducting experiments with the cell lines in a satisfactory manner. These tests would not be possible using factory-delivered coils due to their parameters and the size of the test objects, whose volume did not exceed 1 mL. MRS studies revealed an increase in the metabolite at 1.9 ppm, which indicates the induction of histone acetylation. Changes in histone acetylation play a very important role in both cell development and differentiation processes. The use of Trastuzumab therapy in breast cancer cells increases the levels of acetylated histones. MRS studies and spectra obtained from the 300 MHz NMR system are consistent with the specificity inherent in both systems. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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