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Research Article

Autoantibody Against New Gene Expressed in Prostate Protein is Traceable in Prostate Cancer Patients

, , , , , & show all
Pages 1125-1138 | Received 28 Feb 2018, Accepted 05 Jul 2018, Published online: 07 Sep 2018
 

Abstract

Aim

We assessed an autoantibody against new gene expressed in prostate (NGEP) protein for prostate cancer (PCa) that may better diagnosis and prognosis approaches in the patients with PCa.

Methods

Autoantibodies against NGEP were measured in sera of PCa patients by ELISA.

Results

The autoantibody against NGEP is present in a significantly higher proportion in the sera of PCa patients as compared with healthy controls (p < 0.001). An inverse significant correlation was found between seropositive patients and Gleason score (p < 0.05) and serum prostate-specific antigen (recombinant NGEP; p < 0.05).

Conclusion

The data showed that measurement of autoantibody against NGEP as a novel prostate-specific antigen in sera can be used as a potential biomarker to discriminate well-differentiated PCa patients from normal subjects.

Financial & competing interest disclosure

This study was conducted as a research project and supported by a grant from Iran University of Medical Sciences (grant number: #117-28789) and Iranian National Science Foundation (grant number: #89002533). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

No writing assistance was utilized in the production of this manuscript.

Ethical approval

This study was approved by Iran University of Medical Sciences. All procedures performed in this study were in accordance with the the ethical standards of the Institution at which the study was conducted and the 1964 Helsinki Declaration and its later amendments.

Additional information

Funding

This study was conducted as a research project and supported by a grant from Iran University of Medical Sciences (grant number: #117-28789) and Iranian National Science Foundation (grant number: #89002533). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

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