1. Orexin A associates with inflammation by interacting with OX1R/OX2R receptor and activating prepro-Orexin in cancer tissues of gastric cancer patients.
- Author
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Hu S, Niu J, Zhang R, Li X, Luo M, Sang T, Guo J, Liu J, Ding X, Li X, Ma Y, and Gao R
- Subjects
- Female, Gastritis complications, Gastritis, Atrophic metabolism, Gene Expression Regulation, Neoplastic, Helicobacter Infections complications, Humans, Male, Middle Aged, Neoplasm Grading, Neoplasm Proteins biosynthesis, Neoplasm Proteins genetics, Orexin Receptors biosynthesis, Orexin Receptors genetics, Orexins biosynthesis, Orexins genetics, RNA, Messenger biosynthesis, RNA, Messenger genetics, Stomach Neoplasms microbiology, Stomach Neoplasms pathology, Gastritis metabolism, Helicobacter Infections metabolism, Helicobacter pylori, Neoplasm Proteins physiology, Orexin Receptors physiology, Orexins physiology, Protein Precursors metabolism, Stomach Neoplasms metabolism
- Abstract
Objective: Gastric cancer (GC) has been become the second leading cause for cancer-associated death. This study aimed to investigate Orexin A levels and associated receptors in tumor tissues of GC patients., Patients and Methods: Forty-six consecutive gastric cancer patients (GC, n=46) and 13 chronic atrophic gastritis patients (CAG, n=13) were recruited. Meanwhile, 18 health individuals visiting Medical Examination Department were involved as control (N group, n=18). ELISA was used to examine Orexin A concentration. Immunohistochemistry assay was used to examine OX1R and OX2R. HE staining was applied to evaluate inflammation. qRT-PCR was employed to detect OX1R, OX2R, prepro-Orexin mRNAs. Serum Helicobacter pylori (H. pylori) infection was measured., Results: Orexin A expression in GC patients was significantly up-regulated compared to N group and CAG group (p<0.05). Orexin A expression was increased in CAG group compared to N group (p<0.05). Gastric cancer tissues exhibited significantly obvious inflammation compared to N group and CAG group (p<0.05). OX1R and OX2R expressions were significantly down-regulated in GC group compared to N group and CAG group (p<0.05). OX1R and OX2R were lower significantly in GC group compared to CAG group (p<0.05). Prepro-Orexin was significantly depleted in tumor tissues of GC group compared to N group and CAG group (p<0.05). Orexin A expression was un-associated with gender, age and differential grades (p>0.05). CAG and GC patients demonstrated higher H. pylori infection rates., Conclusion: Orexin A was associated with inflammation by interacting with OX1R/OX2R receptor and activating prepro-Orexin in tumor tissues of gastric cancer patients., (Copyright © 2019. Publicado por Elsevier España, S.L.U.)
- Published
- 2020
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