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Biobanking of prostate cancer tissue is crucial for advancing biomarker-guided precision medicine. However, there is no standardized optimal protocol for biobanking prostatectomy specimens. This study aims to compare the representativeness and sustainability of two biobanking protocols-"Punch" and "Slice"-currently used in Norway. Fresh frozen tissue from 40 radical prostatectomy specimens was biobanked using both the Punch and Slice protocols. Following macroscopic evaluation, a 2 mm thick transverse slice of the prostate (Slice protocol) was collected and stored in an ultra-freezer for future drill biopsy subsampling, guided by histopathological assessment of adjacent formalin-fixed, paraffin-embedded tissue sections. After the slice was collected, five cylindrical tissue samples were punched from the cut surfaces (Punch protocol). Statistical analyses were conducted to compare the sampling precision and time consumption of both protocols. Cancerous tissue was successfully sampled in 87.5% of cases using the Punch protocol and 75% of cases using the Slice protocol. Both methods yielded comparable results in terms of the number of cancerous cores and the ability to sample tissue representing the highest Gleason grade. The mean biobanking time of tissue slices was 4.9 minutes compared to 15.1 minutes for the ready-to-use tissue punches. Both methods have previously been shown to provide high-quality RNA extracts. Both biobanking protocols are effective for sampling prostate cancer tissue, with no significant difference in precision or quality. The choice between protocols should consider factors such as resource availability, tissue quantity, and specific research needs. The Punch protocol is less resource-intensive overall, while the Slice protocol collects vastly more tissue, has a shorter period of ischemia, and provides detailed mapping of biobanked components, allowing for further subsampling at multiple time points.
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http://dx.doi.org/10.1089/bio.2024.0175 | DOI Listing |
J Histotechnol
September 2025
3d.FAB, Université Claude Bernard Lyon 1, CNRS, INSA, CPE-Lyon, Villeurbanne, France.
Histological preparation paraffin embedding is the gold standard method for evaluating tissue structure and composition, whether it is originated from biopsy or engineered . Quite often, deformation and shrinkage occur during the histological preparation, which are difficult to predict and qualify. The present study investigates the morphometric changes in bioprinted hydrogels composed of alginate and gelatine, common tissue engineering materials, focusing on three morphologies: full slabs, porous slabs, and porous cubes.
View Article and Find Full Text PDFJ Virol Methods
September 2025
Department of Virology, Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro, PD, Italy. Electronic address:
Since its emergence in 1996, highly pathogenic avian influenza (HPAI) viruses of the A/Goose/Guangdong/1/96 lineage have diversified into multiple clades, culminating in the 2020-2021 global panzootic caused by H5N1 viruses of the clade 2.3.4.
View Article and Find Full Text PDFJ Cardiovasc Magn Reson
September 2025
Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds, UK. Electronic address:
Background: Cardiac diffusion tensor imaging (cDTI) is sensitive to imaging parameters including the number of unique diffusion encoding directions (ND) and number of repetitions (NR; analogous to number of signal averages or NSA). However, there is no clear guidance for optimising these parameters in the clinical setting.
Methods: Spin echo cDTI data with 2 order motion compensated diffusion encoding gradients were acquired in ten healthy volunteers on a 3T MRI scanner with different diffusion encoding schemes in pseudo-randomised order.
Brain Stimul
September 2025
Research Service, VA San Diego Healthcare System, La Jolla, CA, 92161, USA; NEATLabs, Department of Psychiatry, UC San Diego, La Jolla, CA, 92093, USA; Center of Excellence for Stress and Mental Health, VA San Diego Healthcare System, La Jolla, CA, 92161, USA; Mental Health Care Line, VA San Diego H
Background: Repetitive brain stimulation is hypothesized to bidirectionally modulate excitability, with low-frequency trains decreasing and high-frequency (>5 Hz) trains increasing excitability in the brain. However, most insights on the neuroplastic effects of repetitive stimulation protocols stem from non-invasive human studies (TMS/EEG) or from rodent slice physiology. Here, we developed a rodent experimental preparation enabling imaging of cellular activity during repetitive stimulation protocols in vivo to understand the mechanisms by which brain stimulation modulates excitability of prefrontal cortical neurons.
View Article and Find Full Text PDFJ Magn Reson
August 2025
School of Information Technology and Electrical Engineering, University of Queensland, Brisbane, QLD 4072, Australia. Electronic address:
Gradient coils play a critical role in magnetic resonance imaging (MRI) systems by enabling spatial encoding through generating rapidly switching magnetic fields. However, these time-varying fields induce eddy currents in surrounding conductive structures, leading to gradient field distortions and imaging artifacts. In this study, we propose an automatic eddy current compensation method implemented on a field-programmable gate array (FPGA) platform.
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