Tyrosine 23 Phosphorylation-Dependent Cell-Surface Localization of Annexin A2 Is Required for Invasion and Metastases of Pancreatic Cancer
2011

Role of Annexin A2 in Pancreatic Cancer Metastasis

Sample size: 52 publication 15 minutes Evidence: high

Author Information

Author(s): Zheng Lei, Foley Kelly, Huang Lanqing, Leubner Ashley, Mo Guanglan, Olino Kelly, Edil Barish H., Mizuma Masamichi, Sharma Rajni, Le Dung T., Anders Robert A., Illei Peter B., Van Eyk Jennifer E., Maitra Anirban, Laheru Daniel, Jaffee Elizabeth M.

Primary Institution: Johns Hopkins University School of Medicine

Hypothesis

Is Annexin A2 a key factor in the invasion and metastasis of pancreatic cancer?

Conclusion

Annexin A2 is essential for the invasion and metastasis of pancreatic cancer, and targeting it may provide new therapeutic options.

Supporting Evidence

  • Annexin A2 was identified as a new molecule that promotes pancreatic cancer invasion and metastasis.
  • Knockdown of Annexin A2 expression inhibited the in vitro invasion of pancreatic cancer cells.
  • In vivo studies showed that targeting Annexin A2 prolonged survival in mouse models of pancreatic cancer.

Takeaway

This study found that a protein called Annexin A2 helps pancreatic cancer cells spread, and blocking it could help treat the disease.

Methodology

The study used immunohistochemistry, RNA interference, and mouse models to investigate the role of Annexin A2 in pancreatic cancer.

Potential Biases

Potential bias in patient selection and the interpretation of immunological responses.

Limitations

The study primarily focused on a specific protein and its mechanisms, which may not encompass all factors involved in pancreatic cancer metastasis.

Participant Demographics

Patients with pancreatic ductal adenocarcinoma who participated in a phase II clinical trial.

Statistical Information

P-Value

p<0.0001

Statistical Significance

p<0.0001

Digital Object Identifier (DOI)

10.1371/journal.pone.0019390

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication