Angiogenesis-related genes may be a more important factor than matrix metalloproteinases in bronchopulmonary dysplasia development

Autor: Min Yang, Bo-Lin Chen, Xiao-Jun Duan, Yan-Ni Meng, Lu Chen, Jian-Bao Huang, Yan-Ping Chen, Lin-Rui Li
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Male
Pathology
medicine.medical_specialty
Angiogenesis
Neovascularization
Physiologic

Enzyme-Linked Immunosorbent Assay
Matrix metalloproteinase
MMP9
MMP8
chronic lung disease
THBS1
Gastroenterology
Sensitivity and Specificity
03 medical and health sciences
0302 clinical medicine
Downregulation and upregulation
Internal medicine
mental disorders
bronchopulmonary dysplasia
Pathology Section
medicine
Cluster Analysis
Humans
Oligonucleotide Array Sequence Analysis
business.industry
Gene Expression Profiling
Infant
Newborn

Cancer
Retinopathy of prematurity
medicine.disease
Research Paper: Pathology
premature infant
Matrix Metalloproteinases
030104 developmental biology
030228 respiratory system
Oncology
Bronchopulmonary dysplasia
ROC Curve
Area Under Curve
Female
MMPs
business
Transcriptome
Infant
Premature
Zdroj: Oncotarget
ISSN: 1949-2553
Popis: // Min Yang 1 , Bo-Lin Chen 2 , Jian-Bao Huang 1 , Yan-Ni Meng 1 , Xiao-Jun Duan 1 , Lu Chen 1 , Lin-Rui Li 1 and Yan-Ping Chen 1 1 Respiratory Department 2, Hunan Children’s Hospital, Changsha, Hunan, China 2 Thoracic Medicine Department 2, Hunan Cancer Hospital, Changsha, Hunan, China Correspondence to: Yan-Ping Chen, email: // Keywords : bronchopulmonary dysplasia, chronic lung disease, premature infant, THBS1, MMPs, Pathology Section Received : June 27, 2016 Accepted : January 03, 2017 Published : January 18, 2017 Abstract We characterized the expression profile of angiogenesis-related genes (ARG) and matrix metalloproteinase (MMP) genes in preterm infants, with and without bronchopulmonary dysplasia (BPD). We reanalyzed a gene expression dataset for preterm infants from the Gene Expression Omnibus database using the Gene-Cloud of Biotechnology Information platform. A total of 1,652 genes were differentially (1.2-fold change) expressed: 811 were highly expressed in infants with BPD, and 841 were highly expressed in those without BPD. Twenty-eight and 11 ARGs were upregulated in infants with and without BPD, respectively. Among 27 detected MMPs and TIMPs, MMP8, MMP9, MMP25, TIMP2 and TIMP3 were differently expressed. Levels of THBS1, MMP8, MMP9, MMP25, TIMP2 and TIMP3 increased as severity of BPD and retinopathy of prematurity (ROP) increased, whereas ETS1, LEF1 and SPOCK2 exhibited the opposite trend. Expression of ETS1 and LEF1 had a fitting rate of R 2 = 0.849 and P < 0.001. ELISAs showed a positive correlation between THBS1 and CD36 (receptor of THBS1) levels in serum samples from preterm infants. Our study indicates that the upregulation of THBS1 and downregulation of ETS1, LEF1 promotes BPD in preterm infants by disrupting blood vessel formation rather than by dysregulation of MMPs and TIMPs.
Databáze: OpenAIRE