7 results match your criteria: "The First Affiliated Hospital to PLA General Hospital[Affiliation]"

Article Synopsis
  • Fibrosis, linked to collagen production by fibroblasts, is influenced by inflammatory responses, particularly through the regulation of miR-155.
  • Research indicated that reducing miR-155 in macrophages lowers their secretion of TGF-β1 and IL-1β, leading to decreased fibroblast growth and collagen synthesis.
  • The study identified SHIP1 as a target of miR-155, and confirmed involvement of the PI3K/Akt pathway, suggesting that targeting miR-155 may offer new treatment options for skin fibrosis.
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[Advance on human umbilical cord mesenchymal stem cells for treatment of ALI in severe burns].

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue

January 2017

Graduate School, Jinzhou Medical University, Jinzhou 121000, Liaoning, China (Wang Y); Department of Pediatrics, the First Affiliated Hospital to PLA General Hospital, Beijing 100048, China (Hu XH). Corresponding author: Hu Xiaohong, Email:

Severe burn is often accompanied by multiple organ damage. Acute lung injury (ALI) is one of the most common complications, and often occurs in the early stage of severe burns. If it is not treated in time, it will progress to acute respiratory distress syndrome (ARDS), which will be a serious threat to the lives of patients.

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miR-155 promotes cutaneous wound healing through enhanced keratinocytes migration by MMP-2.

J Mol Histol

April 2017

Department of Burns and Cutaneous Surgery, Xijing Hospital, The Fourth Military Medical University, 127 Changle West Road, Xi'an, 710032, Shaanxi, China.

Inflammation, re-epithelization and tissue remodeling are three essential steps during wound healing. The re-epithelization process plays the most important role which mainly involves keratinocyte proliferation and migration. miR-155 has been reported to participate in cell migration and transformation, however, its function in skin wound healing is largely unknown.

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Anti-PD-1/PD-L1 antibody therapy for pretreated advanced nonsmall-cell lung cancer: A meta-analysis of randomized clinical trials.

Medicine (Baltimore)

August 2016

Department of Respiratory and Critical Care Medicine, Changhai Hospital, Second Military Medical University Department of Pulmonary Medicine, Medicine, 85 Hospital of People's Liberation Army, Shanghai Department of Oncology, The First Affiliated Hospital to PLA General Hospital, Beijing, P.R. China.

Background: Anti-PD-1/PD-L1 antibody therapy is a promising clinical treatment for nonsmall-cell lung cancer (NSCLC). However, whether anti-PD-1/PD-L1 antibody therapy can provide added benefits for heavily pretreated patients with advanced NSCLC and whether the efficacy of anti-PD-1/PD-L1 antibody therapy relates to the tumor PD-L1 expression level remain controversial. Thus, this meta-analysis evaluated the efficacy and safety of anti-PD-1/PD-L1 antibody therapy for pretreated patients with advanced NSCLC.

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The hMSCs have become a promising approach for inflammation treatment in acute phase. Our previous study has demonstrated that human umbilical cord-MSCs could alleviate the inflammatory reaction of severely burned wound. In this study, we further investigated the potential role and mechanism of the MSCs on severe burn-induced excessive inflammation.

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Mesenchymal stem cell (MSC)-derived exosomes have diverse functions in regulating wound healing and inflammation; however, the molecular mechanism of human umbilical cord MSC (hUCMSC)-derived exosomes in regulating burn-induced inflammation is not well understood. We found that burn injury significantly increased the inflammatory reaction of rats or macrophages exposed to lipopolysaccharide (LPS), increased tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β) levels and decreased IL-10 levels. hUCMSC-exosome administration successfully reversed this reaction.

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Hyperglycemia is one of the most important clinical features of burn patients. Previous reports had demonstrated that miRNA was involved in regulating glucose metabolism in various diseases such as diabetes and obesity. Our current study discovered the relationship between miR-194 and hyperglycemia in burn rats via suppressing insulin-like growth factor 1 receptor (IGF-IR).

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