74 results match your criteria: "The Second Xiangya Hospital Central South University[Affiliation]"

Assembly of a biomimetic copper-based nanocomplex for alleviating hypoxia to enhance cuproptosis against osteosarcoma and lung metastasis.

Acta Biomater

December 2024

Department of Orthopedics, The Second Xiangya Hospital, Central South University, Changsha, China; Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital, Changsha, China. Electronic address:

Osteosarcoma tissues demonstrated elevated expression of proteins (FDX1 and DLAT) integral to cuproptosis in our preliminary study, indicating the potential effectiveness of anti-tumor strategies predicated on this process. Nevertheless, the overexpression of copper export proteins and the challenge of copper ion penetration may contribute to insufficient local copper ion concentration for inducing cuproptosis. Herein, we engineered a biomimetic copper-elesclomol-polyphenol network for the efficient delivery of copper ions and the copper ionophore elesclomol.

View Article and Find Full Text PDF

Programmed cell death represents a precisely regulated and active cellular demise, governed by a complex network of specific genes and proteins. The identification of multiple forms of programmed cell death has significantly advanced the understanding of its intricate mechanisms, as demonstrated in recent studies. A thorough grasp of these processes is essential across various biological disciplines and in the study of diseases.

View Article and Find Full Text PDF

Aims/hypothesis: Upregulation of serum leucine-rich α-2-glycoprotein 1 (LRG1) has been implicated in diet-induced obesity and metabolic disorders. However, its specific hormonal actions remain unclear. This study aimed to determine whether diet-enhanced serum LRG1 levels promote hyperinsulinaemia by directly stimulating insulin secretion from pancreatic beta cells.

View Article and Find Full Text PDF
Article Synopsis
  • Acute kidney injury (AKI) is characterized by a rapid decrease in kidney function due to various causes, and the role of the transcription factor PRDM16 in this condition is being researched.
  • PRDM16 was found to inhibit cell death caused by ischemia/reperfusion injury in kidney cells by regulating the expression of S100A6 and targeting specific signaling pathways.
  • In experiments, PRDM16 showed protective effects against AKI, while its absence worsened the condition in genetically modified mice, indicating its potential as a therapeutic target.
View Article and Find Full Text PDF

This study aimed to investigate the effects and molecular mechanism of PF on high glucose (HG)-induced podocyte injury. Results found that PF increased proliferation activity, decreased apoptosis, LDH, and caspase-3 levels, and increased nephrin and podocin expression in HG-induced cells. Similarly, PF improved HG-induced mitochondrial damage, decreased Ca and ROS content, alleviated oxidative stress, inhibited mPTP opening, increased mitochondrial membrane potential, and decreased the expressions of Drp1, Bak, Bax, and Cytc in cytoplasm, increased the expressions of SIRT1, PGC-1α, HSP70, HK2, and Cytc in mitochondria of podocytes.

View Article and Find Full Text PDF

Hearing impairment is a global health problem that affects social communications and the economy. The damage and loss of cochlear hair cells and spiral ganglion neurons (SGNs) as well as the degeneration of neurites of SGNs are the core causes of sensorineural hearing loss. Biotechnologies and biomedical engineering technologies provide new hope for the treatment of auditory diseases, which utilizes biological strategies or tissue engineering methods to achieve drug delivery and the regeneration of cells, tissues, and even organs.

View Article and Find Full Text PDF

Despite significant progress in therapy, there remains a lack of substantial evidence regarding the molecular factors that lead to renal fibrosis. Neuraminidase 4 (NEU4), an enzyme that removes sialic acids from glycoconjugates, has an unclear role in chronic progressive fibrosis. Here, this study finds that NEU4 expression is markedly upregulated in mouse fibrotic kidneys induced by folic acid or unilateral ureter obstruction, and this elevation is observed in patients with renal fibrosis.

View Article and Find Full Text PDF

Background: The association between poor cardiovascular health and cognitive decline as well as dementia progression has been inconsistent across studies. This study used Mendelian randomization (MR) to investigate the causal relationship between Alzheimer disease (AD), circulating levels of total-tau, and coronary artery disease (CAD).

Methods And Results: This study used MR to investigate the causal relationship between AD or circulating levels of total-tau and CAD, including ischemic heart disease, myocardial infarction, coronary heart disease, coronary atherosclerosis, and heart failure.

View Article and Find Full Text PDF

Acute asthma exacerbation refers to the progressive deterioration of asthma symptoms that is always triggered by virus infection represented by respiratory syncytial virus (RSV). After RSV infection, exaggerated Th2-mediated pulmonary inflammation is the critical pathological response of asthmatic patients with acute exacerbation. Significantly, airway epithelial cells, being the primary targets of RSV infection, play a crucial role in controlling the pulmonary inflammatory response by releasing airway epithelial cell-derived exosomes (AEC-Exos), which potentially influence the development of asthma.

View Article and Find Full Text PDF

Coffee, a widely consumed beverage, has shown benefits for human health but lacks sufficient basic and clinical evidence to fully understand its impacts and mechanisms. Here, we conducted a cross-sectional observational study of coffee consumption and a 1-month clinical trial in humans. We found that coffee consumption significantly reshaped the immune system and metabolism, including reduced levels of inflammatory factors and a reduced frequency of senescent T cells.

View Article and Find Full Text PDF
Article Synopsis
  • Lateral suspension is a surgical procedure designed to fix apical prolapse by placing T-shaped mesh in the abdomen, but there’s no consensus on its safety or indications.
  • A Delphi process involved 21 international expert surgeons discussing and reaching agreement on various aspects of laparoscopic lateral suspension (LLS) through rounds of statements and discussions.
  • The consensus highlighted LLS as a safe and effective method for treating pelvic organ prolapse, along with key technical details and indications for the procedure.
View Article and Find Full Text PDF

Stratified Treatment in Pediatric Anaplastic Large Cell Lymphoma: Result of a Prospective Open-Label Multiple-Institution Study.

Cancer Res Treat

October 2024

Department of Pediatric Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in Southern China, and Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.

Purpose: The risk stratification of pediatric anaplastic large cell lymphoma (ALCL) has not been standardized. In this study, new risk factors were included to establish a new risk stratification system for ALCL, and its feasibility in clinical practice was explored.

Materials And Methods: On the basis of the non-Hodgkin's lymphoma Berlin-Frankfurt-Munster 95 (NHL-BFM-95) protocol, patients with minimal disseminated disease (MDD), high-risk tumor site (multiple bone, skin, liver, and lung involvement), and small cell/lymphohistiocytic (SC/LH) pathological subtype were enrolled in risk stratification.

View Article and Find Full Text PDF

Background: Allergic asthma is a heterogeneous disease and new strategies are needed to prevent or treat this disease. Studies have shown that probiotic interventions are effective in preventing asthma. Here, we investigated the impact of Saccharomyces boulardii (S.

View Article and Find Full Text PDF

Correction to: Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathway.

MedComm (2020)

February 2024

Department of Nephrology National Clinical Research Center for Geriatric Disorders Xiangya Hospital, Central South University Changsha China.

[This corrects the article DOI: 10.1002/mco2.226.

View Article and Find Full Text PDF
Article Synopsis
  • Marfan syndrome (MFS) is a genetic disorder linked to the FBN1 gene, impacting the skeletal, cardiopulmonary, and ocular systems, prompting research into how epigenetics influences the variability of symptoms in the disease.
  • Using the Illumina 850K DNA methylation array, researchers examined blood samples from patients with MFS and healthy individuals, identifying 1253 differentially methylated positions (DMPs) associated primarily with conditions like scoliosis and cardiomyopathy.
  • The findings suggest a crucial link between DNA methylation changes and clinical features in MFS, potentially leading to insights about why untreated patients experience severe symptoms and reduced lifespan.
View Article and Find Full Text PDF

Objective: To investigate the relationship between icariin and the osteoblastic differentiation of vascular smooth muscle cells (VSMCs) and the signal pathway involved.

Methods: We applied a universally accepted calcification model of VSMCs induced by β glycerophosphate. Then the VSMCs calcification was observed by treatment with icariin and/or inhibitors of estrogen receptors (ERs) and p38-mitogen-activated protein kinase (MAPK) signaling.

View Article and Find Full Text PDF

Objective: To investigate the incidence of falls in elderly aged 65 years and above among outpatients and inpatients, and to analyze its related factors and identify prevention strategies.

Methods: A retrospective analysis was conducted on 451 patients aged 65 years and above who received comprehensive geriatric assessment in outpatients and inpatients from the Department of Geriatrics in the Second Xiangya Hospital from March 2021 to March 2022. According to whether there had been at least one fall in the past year, the patients were divided into a fall group and a non-fall group.

View Article and Find Full Text PDF

Malignant tumors are one of the leading causes of death which impose an increasingly heavy burden on all countries. Therefore, the establishment of research models that closely resemble original tumor characteristics is crucial to further understanding the mechanisms of malignant tumor development, developing safer and more effective drugs, and formulating personalized treatment plans. Recently, organoids have been widely used in tumor research owing to their advantages including preserving the structure, heterogeneity, and cellular functions of the original tumor, together with the ease of manipulation.

View Article and Find Full Text PDF

Colon adenocarcinoma (COAD) is a type of cancer that arises from the glandular epithelial cells that produce mucus in the colon. COAD is influenced by various factors, including genetics, environment and lifestyle. The outcome of COAD is determined by the tumor stage, location, molecular characteristics and treatment.

View Article and Find Full Text PDF
Article Synopsis
  • Despite advancements, treatment options for osteosarcoma remain limited, prompting research using RNA sequencing, proteomics, and drug screening to identify potential therapeutic targets.
  • The study identified over 2500 genes and hundreds of drug combinations, revealing important targets like HDAC1 and TOP2A that play vital roles in osteosarcoma.
  • The findings showed that combining HDAC inhibitors with doxorubicin (DOX) effectively suppressed osteosarcoma growth by altering key gene expressions.
View Article and Find Full Text PDF

Objective: The purpose of this study was to investigate the relationship between bedtime at night and the risk of diabetes in adults.

Methods: We extracted data from 14,821 target subjects from the NHANES database for a cross-sectional study. The data on bedtime came from the question in the sleep questionnaire: "What time do you usually fall asleep on weekdays or workdays?".

View Article and Find Full Text PDF

Gene therapy, a medical approach that involves the correction or replacement of defective and abnormal genes, plays an essential role in the treatment of complex and refractory diseases, such as hereditary diseases, cancer, and rheumatic immune diseases. Nucleic acids alone do not easily enter the target cells due to their easy degradation in vivo and the structure of the target cell membranes. The introduction of genes into biological cells is often dependent on gene delivery vectors, such as adenoviral vectors, which are commonly used in gene therapy.

View Article and Find Full Text PDF