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The renewed interest in ultra-low-field MRI (< 0.1 T), with its advantages of cost-effectiveness and portability, is expected to drive a paradigm shift from traditional MRI scanners to point-of-care imaging systems. Here, we characterized the in vivo T and T relaxation times of healthy breast tissues using quantitative MRI at 50 mT to advance the development of ultra-low-field breast MRI methodologies. First, the developed in vivo quantitative mapping protocols were tested and validated using CuSO-doped water phantom experiments on the custom-built 50-mT MRI prototype. Then, in vivo quantitative T and T mapping of human breast tissues was measured in healthy female subjects. The T and T values for fat tissue, fibrous tissue, and glandular tissue components were determined using an automatic segmentation method based on the relaxation times. The mean T times were 121.21 ± 14.57, 182.26 ± 20.96, and 238.32 ± 10.71 ms for fat tissue, fibrous tissue, and glandular tissue, respectively. While the mean T times were 111.36 ± 14.28 and 69.44 ± 15.26 ms for fat tissue and fibroglandular tissue, respectively. For healthy breast tissues, the significantly shorter T times at 50 mT are favorable for improving the imaging speed. T times are similar to those seen at conventional clinical field strengths. Additionally, the relatively small difference in T times between fibrous tissue and glandular tissue made it difficult to segment these two tissues independently. This work can provide a valuable reference for future breast tissues diagnostic imaging in ultra-low-field MRI scenarios, thereby promoting the wider adoption of portable breast MRI in routine breast disease screening.
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http://dx.doi.org/10.1002/nbm.70081 | DOI Listing |
Int J Nanomedicine
September 2025
School of Pharmaceutical Sciences, Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases, Zhengzhou University, Zhengzhou, 450001, People's Republic of China.
Purpose: This study aimed to develop a composite nanozyme system (Au/PB-Ce6-HA) based on gold nanoparticles (AuNPs) and Prussian blue nanoparticles (PBNPs) to combat tumor hypoxia and insufficient endogenous hydrogen peroxide (HO) deficiency, thus enhancing the efficacy of sonodynamic therapy (SDT) and starvation therapy for liver cancer.
Methods: The Au/PB-Ce6-HA system was constructed by in situ embedding AuNPs on PBNPs, loading the sonosensitizer Chlorin e6 (Ce6), and surface-coating with thiolated hyaluronic acid (HA-SH). The system was evaluated both in vitro and in vivo to assess its ability to catalyze glucose to generate HO, decompose HO to produce oxygen, and generate highly toxic reactive oxygen species (ROS) under ultrasound irradiation.
Oncol Res
September 2025
Koltzov Institute of Developmental Biology, Russian Academy of Sciences, Moscow, 119334, Russia.
Objectives: Proteasomes, multi-subunit proteases, are key actors of cellular protein catabolism and a number of regulatory processes. The detection of subtle proteasome functioning in tumors may contribute to our understanding of the mechanisms of cancer development. The current study aimed to identify the role of low molecular mass protein 2 (LMP2), a proteasome immune subunit, in the development of mouse colon 26 (C26) adenocarcinoma.
View Article and Find Full Text PDFFront Immunol
September 2025
Department of Digestive Oncology, The Third Affiliated Hospital of Kunming Medical University, Yunnan Cancer Hospital, Peking University Cancer Hospital Yunnan, Kunming, Yunnan, China.
Objectives: Circular RNAs (circRNAs) are a class of non-coding RNAs with diverse pathophysiological functions. However, the functional roles and molecular mechanisms of circRNAs in lung adenocarcinoma (LUAD) remain to be further elucidated.
Methods: The expression levels of Circ_0007552 (Circ_RILPL1), miR-7974, and BRCA1-associated protein 1 (BAP1) mRNA in LUAD tissues and cells were detected by quantitative real-time PCR (qRT-PCR).
Front Med (Lausanne)
August 2025
First Clinical Medical School, Gansu University of Chinese Medicine, Lanzhou, Gansu Province, China.
Background: Carbon-ion radiotherapy (CIRT) is an advanced form of high linear energy transfer (LET) radiotherapy that has demonstrated superior biological effectiveness compared to conventional photon therapy in the treatment of various malignancies; however, its role in gastric cancer remains unclear. Dihydroorotate dehydrogenase (DHODH), a key enzyme implicated in cancer progression, has been linked to tumor radiosensitivity. This study aims to investigate whether CIRT inhibits gastric cancer progression via the regulation of DHODH.
View Article and Find Full Text PDFTurk J Biol
June 2025
Xu Rongxiang Regenerative Medicine Research Center, Binzhou Medical University, Yantai, P.R. China.
Background: Abdominal aortic aneurysm (AAA), a gradual segmental dilatation of the abdominal aorta, is associated with a high mortality rate. The pathophysiological molecular mechanisms underlying AAA remain unclear. In recent years, changes in miRNA levels have been reported to be involved in the development and treatment of AAA.
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