Objective: To determine the proportion of intravoxel incoherent motion diffusion-weighted images (IVIM-DWI) and three-dimensional arterial circulation markers (3D-ASL) in Ki-67 labeling index (Ki-67 LI) and glioma grading.
Methods: According to the classification of diseases of the central nervous system dealt with by WHO in 2007, patients with stage II glioma were classified as low ( = 20) and patients with stages III-IV were divided into higher levels ( = 22). Prior to surgery, brain MRI, IVIM-DWI, and 3D-ASL were performed in all patients, and the actual water molecular diffusion coefficient (), microcirculation coefficient (∗), blood flow fraction (), and cerebral blood flow (CBF) were measured. A rank sum (Mann-Whitney test) was used to compare the four upper and lower level Ki-67 LI measurements. Spearman's method is used to identify the relationship between 4 groups of quantification and Ki-67 LI. Reciprocal grafting (ROC) curves were used to measure the diagnosis of four groups of glioma grading defects.
Results: There were significant differences in , ∗, , and CBF between the solid region of the tumor and the normal white matter contralateral to it ( < 0.05). The significant differences of , ∗, , and CBF were shown between patients with low-grade glioma and high-grade glioma ( < 0.05). Ki-67 LI was found to have negative correlation with ( = 00.693, < 0.001) and ( = 00.539, < 0.001), but similarly correlated with CBF ( = 0.665, < 0.001) in patients with glioma. Recipient efficacy for predicting advanced and secondary glioma from , , ∗, CBF, and Ki-67 LI raises AUCs of 0.819, 0.747, 0.719, 0.836, and 0.907, respectively.
Conclusion: IVIM-DWI has good application value for preoperative grading of glioma.
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http://dx.doi.org/10.1155/2022/8429659 | DOI Listing |
Plant Physiol Biochem
December 2024
Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. Electronic address:
Front Physiol
January 2021
Department of Renal and Body Fluid Physiology, Mossakowski Medical Research Institute, Polish Academy of Sciences, Warsaw, Poland.
Cytochrome P450 (CYP-450) metabolites of arachidonic acid: epoxyeicosatrienoic acids (EETs) and 20-hydroxyeicosatetraenoic acid (20-HETE) have established role in regulation of blood pressure (BP) and kidney function. EETs deficiency and increased renal formation of 20-HETE contribute to hypertension in spontaneously hypertensive rats (SHR). We explored the effects of 14,15-EET analog (EET-A) and of 20-HETE receptor blocker (AAA) on BP and kidney function in this model.
View Article and Find Full Text PDFAutophagy
October 2016
kb Emory University, School of Medicine, Department of Microbiology and Immunology , Atlanta , GA , USA.
J Virol
November 2014
First Hospital of Jilin University, Institute of Virology and AIDS Research, Changchun, Jilin, China Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA Collaborative Innovation Center of Chemical Science and Engineering, School of Life Sciences, Tianjin University, Tianjin, China
Unlabelled: Human immunodeficiency virus type 1 (HIV-1) and simian immunodeficiency virus (SIV) viral infectivity factor (Vif) form a CRL5 E3 ubiquitin ligase complex to suppress virus restriction by host APOBEC3 (A3) proteins. The primate lentiviral Vif complex is composed of the unique cofactor core binding factor β (CBF-β) and canonical ligase components Cullin 5 (CUL5), Elongin B/C (ELOB/C), and RBX2. However, the mechanism by which the Vif protein of the related lentivirus bovine immunodeficiency virus (BIV) overcomes its host A3 proteins is less clear.
View Article and Find Full Text PDFRetrovirology
August 2013
National Engineering Laboratory for AIDS Vaccine, College of Life Science, Jilin University, Changchun, Jilin Province, People's Republic of China.
Background: The HIV-1 accessory factor Vif is necessary for efficient viral infection in non-permissive cells. Vif antagonizes the antiviral activity of human cytidine deaminase APOBEC3 proteins that confer the non-permissive phenotype by tethering them (APOBEC3DE/3F/3G) to the Vif-CBF-β-ElonginB-ElonginC-Cullin5-Rbx (Vif-CBF-β-EloB-EloC-Cul5-Rbx) E3 complex to induce their proteasomal degradation. EloB and EloC were initially reported as positive regulatory subunits of the Elongin (SIII) complex.
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