STAT5A modulates gastric cancer progression via upregulation of CD44.

Genomics

Research Center of Basic Medicine, Jinan Central Hospital, Shandong University, 56# Shanda South Road, Jinan, Shandong 250013, People's Republic of China; Research Center of Basic Medicine, Jinan Central Hospital, Shandong First Medical University, 56# Shanda South Road, Jinan, Shandong 250013, People's Republic of China. Electronic address:

Published: May 2023

AI Article Synopsis

  • STAT5A is frequently phosphorylated in tumors and is linked to gastric cancer progression, although its specific role and targets are not well-understood.
  • Researchers investigated the expression of STAT5A and CD44 in gastric cancer cells and in animal models to assess their biological functions.
  • Results indicate that increased phosphorylated STAT5A correlates with tumor invasion and poor prognosis, as it enhances gastric cancer cell proliferation by upregulating CD44, suggesting that the STAT5A/CD44 pathway is crucial for gastric cancer development.

Article Abstract

Objective: Signal transduction and transcriptional activator 5A (STAT5A), which has been reported to be frequently phosphorylated in tumors, plays pivotal roles in tumor progression. However, the role of STAT5A in gastric cancer (GC) progression and the downstream targets of STAT5A remain largely unknown.

Methods: The expression of STAT5A and CD44 were assessed. GC cells were treated with altered STAT5A and CD44 to evaluate their biological functions. Nude mice were given injections of genetically manipulated GC cells and growth of xenograft tumors and metastases was measured.

Results: The increased level of p-STAT5A is associated with tumor invasion and poor prognosis in GC. STAT5A promoted GC cell proliferation by upregulating CD44 expression. STAT5A directly binds to the CD44 promoter and promotes its transcription.

Conclusions: The STAT5A/CD44 pathway plays a critical role in GC progression, promising potential clinical applications for improving treatment of GC.

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Source
http://dx.doi.org/10.1016/j.ygeno.2023.110638DOI Listing

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