Your browser doesn't support javascript.
loading
Circ8199 encodes a protein that inhibits the activity of OGT by JAK2-STAT3 pathway in esophageal squamous cell carcinoma.
Li, Chen-Jia; Li, Dong-Ge; Liu, En-Jie; Jiang, Guo-Zhong.
Affiliation
  • Li CJ; Department of Pathology, School of Basic Medicine, Zhengzhou University Zhengzhou 450001, Henan, PR China.
  • Li DG; Department of Pathology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052, Henan, PR China.
  • Liu EJ; Luoyang Traditional Chinese Medicine Hospital Luoyang 471099, Henan, PR China.
  • Jiang GZ; Department of Pathology, School of Basic Medicine, Zhengzhou University Zhengzhou 450001, Henan, PR China.
Am J Cancer Res ; 13(3): 1107-1117, 2023.
Article in En | MEDLINE | ID: mdl-37034230
ABSTRACT
Esophageal squamous cell carcinoma (ESCC) is an invasive malignant tumor with a high incidence rate and mortality. It is imperative to study its tumorigenesis and development for better treatment. CircRNA has been proven to play an important role in various cancers. Our previous studies found that the circ8199 gene is associated with tumor prognosis. To further clarify the role of circ8199 in ESCC, we performed functional experiments and found that overexpression of circ8199 significantly inhibited the proliferation of ESCC cells and the activity of O-linked N-acetylglucosamine transferase (OGT) simultaneously. Further experiments demonstrated that circ8199 could interact with OGT, leading to a decrease in OGT's activity. The reduction of circ8199 expression stimulated the binding activity between OGT and its downstream gene JAK2, promoting the O-GlcNAc glycosylation modification of JAK2 and activating the JAK2-STAT3 pathway. Our study indicated that circ8199 regulates the JAK2-STAT3 pathway through OGT, providing a candidate mechanism for drug discovery and development.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Am J Cancer Res Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Language: En Journal: Am J Cancer Res Year: 2023 Type: Article