Assessment of apelin, apelin receptor, resistin, and adiponectin levels in the primary tumor and serum of patients with esophageal squamous cell carcinoma.
Adiponectin
/ blood
Apelin
/ blood
Apelin Receptors
/ blood
Biomarkers, Tumor
/ blood
Carcinoma, Squamous Cell
/ metabolism
Case-Control Studies
Enzyme-Linked Immunosorbent Assay
Esophageal Neoplasms
/ blood
Esophageal Squamous Cell Carcinoma
/ blood
Humans
Lymph Nodes
Lymphatic Metastasis
Neoplasm Metastasis
/ pathology
Prognosis
RNA, Messenger
Resistin
/ blood
Reverse Transcriptase Polymerase Chain Reaction
adipokines
apelin
apelin receptor
esophageal squamous cell carcinoma
Journal
Advances in clinical and experimental medicine : official organ Wroclaw Medical University
ISSN: 1899-5276
Titre abrégé: Adv Clin Exp Med
Pays: Poland
ID NLM: 101138582
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
pubmed:
15
1
2019
medline:
10
8
2019
entrez:
15
1
2019
Statut:
ppublish
Résumé
Disturbances in adipokine secretion are associated with the risk of cancer growth and progression. The aim of the study was to evaluate the mRNA expression and protein levels of apelin, the apelin receptor, resistin, and adiponectin in the tumor tissues of surgically treated esophageal squamous cell carcinoma (ESCC) patients. Concentrations of serum adipokines were assessed in relation to ESCC progression. The study group consisted of 53 patients with ESCC and 27 controls. In the ESCC group, 27 patients were surgically treated and 26 were treated with palliative procedures. RT-PCR and ELISA tests were used to measure the mRNA expression and protein level of adipokines in tissues and their concentration in serum. We found that mRNA expression and protein concentrations of apelin, the apelin receptor and resistin were significantly higher in tumor tissue than in control tissue. The protein concentration of apelin were significantly increased in the tumors of patients with lymph node metastasis (p < 0.005). Circulating levels of apelin, the apelin receptor and resistin were significantly higher in the cancer patients than in controls (p < 0.05 for all). The concentration of serum apelin receptor significantly decreased in patients with stage IV cancer, the presence of lymph node or distant metastasis (p < 0.05). Apelin may participate in lymphangiogenesis and the progression of ESCC. The apelin receptor is intensely produced in the early stage of cancer development and it may take part in the carcinogenic processes of ESCC.
Sections du résumé
BACKGROUND
BACKGROUND
Disturbances in adipokine secretion are associated with the risk of cancer growth and progression.
OBJECTIVES
OBJECTIVE
The aim of the study was to evaluate the mRNA expression and protein levels of apelin, the apelin receptor, resistin, and adiponectin in the tumor tissues of surgically treated esophageal squamous cell carcinoma (ESCC) patients. Concentrations of serum adipokines were assessed in relation to ESCC progression.
MATERIAL AND METHODS
METHODS
The study group consisted of 53 patients with ESCC and 27 controls. In the ESCC group, 27 patients were surgically treated and 26 were treated with palliative procedures. RT-PCR and ELISA tests were used to measure the mRNA expression and protein level of adipokines in tissues and their concentration in serum.
RESULTS
RESULTS
We found that mRNA expression and protein concentrations of apelin, the apelin receptor and resistin were significantly higher in tumor tissue than in control tissue. The protein concentration of apelin were significantly increased in the tumors of patients with lymph node metastasis (p < 0.005). Circulating levels of apelin, the apelin receptor and resistin were significantly higher in the cancer patients than in controls (p < 0.05 for all). The concentration of serum apelin receptor significantly decreased in patients with stage IV cancer, the presence of lymph node or distant metastasis (p < 0.05).
CONCLUSIONS
CONCLUSIONS
Apelin may participate in lymphangiogenesis and the progression of ESCC. The apelin receptor is intensely produced in the early stage of cancer development and it may take part in the carcinogenic processes of ESCC.
Substances chimiques
Adiponectin
0
Apelin
0
Apelin Receptors
0
Biomarkers, Tumor
0
RNA, Messenger
0
Resistin
0
Types de publication
Evaluation Study
Journal Article
Langues
eng