The detection of vitality of wounds, especially when the wounds are inflicted very close to the time of death, is one of the most challenging issues in forensic pathology. This study investigated expression levels of ATF3 and BTG2 in mouse and human skin wounds. Protein levels examined by western blot showed that there was no significant change in ATF3 and BTG2 between wounded and intact skins. However, mRNA levels demonstrated higher expression of ATF3 and BTG2 in ante-mortem contused mouse skins, compared with the intact and postmortem contused skins. Increased ATF3 and BTG2 in the level of mRNA could also be detected until 96h and 48h after death, respectively. Human wounded skin samples from forensic autopsy cases were also examined. Increased ATF3 mRNA levels were detected until 48h after autopsy in 5 of 6 cases. However, no differences were observed between wounded and intact skins for BTG2. These findings suggest that the detection of mRNA levels of ATF3, but not BTG2, can be considered as a potential marker for vital reaction of skin contusion. Postmortem human samples should be used in order to validate the availability of markers screened by animal experiment.
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http://dx.doi.org/10.1016/j.forsciint.2019.109937 | DOI Listing |
J Integr Neurosci
July 2024
Department of Pediatrics, Beijing Friendship Hospital, Capital Medical University, 100050 Beijing, China.
Background: Hypoxic-ischemic injury of neurons is a pathological process observed in several neurological conditions, including ischemic stroke and neonatal hypoxic-ischemic brain injury (HIBI). An optimal treatment strategy for these conditions remains elusive. The present study delved deeper into the molecular alterations occurring during the injury process in order to identify potential therapeutic targets.
View Article and Find Full Text PDFMedicine (Baltimore)
September 2023
College of Environment and Public Health, Xiamen Huaxia University, Xiamen, P.R. China.
Currently, the incidence of diabetes mellitus is increasing rapidly, particularly in China, and its pathogenesis is still unclear. The goal of this study was to find meaningful biomarkers of metastasis in patients with diabetes and cancer using bioinformatic analysis in order to predict gene expression and prognostic importance for survival. We used the Differentially Expressed Gene, Database for Annotation Visualization and Integrated Discovery, and Gene Set Enrichment Analyses databases, as well as several bioinformatics tools, to explore the key genes in diabetes.
View Article and Find Full Text PDFGene
March 2023
Department of Orthopaedics, the Second Affiliated Hospital of Kunming Medical University, China. Electronic address:
Background: Early-onset scoliosis (EOS) is a scoliosis deformity caused by various reasons before the age of 10 years and is often combined with thoracic insufficiency syndrome (TIS) causing patients with difficulty in securing lung growth in the thoracic cage. Currently, there is a shortage of effective large animal models for evaluating EOS + TIS in therapeutic studies. Consequently, we propose to construct a porcine EOS + TIS model and evaluate its transcriptome changes by RNA sequencing.
View Article and Find Full Text PDFSci Transl Med
August 2022
King Abdullah University of Science and Technology (KAUST), Biological Environmental Sciences and Engineering Division BESE, KAUST Environmental Epigenetics Program, Thuwal, Saudi Arabia.
Constitutive heterochromatin is responsible for genome repression of DNA enriched in repetitive sequences, telomeres, and centromeres. During physiological and pathological premature aging, heterochromatin homeostasis is profoundly compromised. Here, we showed that () RNA accumulation was an early event in both typical and atypical human progeroid syndromes.
View Article and Find Full Text PDFCrit Rev Eukaryot Gene Expr
April 2022
Department of Joint, Tianjin Hospital, No. 406 Jiefang South Rd, Hexi District, Tianjin 300211, China.
Osteoarthritis (OA) is a severe disease and has brought a massive burden to people's daily life. This study was performed to explore the hub genes associated with OA and predict potential biomarkers for OA. The cartilage (GSE114007) and synovial (GSE55235 and GSE55457) datasets downloaded from the Gene Expression Omnibus (GEO) database were used to screen the differentially expressed genes in OA compared with normal tissues.
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