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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2009, Vol. 14 ›› Issue (9): 1018-1022.

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Expression and significance of signal transducer and activator of transcription 6 and prostate-specific antigen proteins in prostatic carcinoma

CHEN Rong-sheng1, LUO Dong-jiao2, CHEN Li1, TONG Xia-sheng3, CHEN Hao4, WANG Enzhi5   

  1. 1Department of Urinary Surgery, Taizhou Integrated Western and Traditional Chinese Medicine Hospital, Affiliated to the First Clinical Medicine of Zhejiang Chinese Medical University, Wenling 317523, Zhejiang, China;
    2Department of Medical Science, Qianjiang College, Hangzhou Normal University, Hangzhou 310012, Zhejiang, China;
    3Department of Pediatrics, 4Department of Pathology, 5Department of Clinical Laboratory, Taizhou Integrated Western and Traditional Chinese Medicine Hospital, Affiliated to the First Clinical Medicine of Zhejiang Chinese Medical University, Wenling 317523, Zhejiang, China
  • Received:2009-06-18 Revised:2009-08-09 Published:2020-11-03

Abstract: AIM: To observe the expressions of signal transducer and activator of transcription (STAT)- 6 and prostate-specific antigen(PSA) proteins in prostatic carcinoma, and approach the pathogenesis and early diagnosis methods of prostatic carcinoma. METHODS: All patients were operated during January 2005 to May 2008 including 20 cases of prostatic carcinoma and 36 cases of benign prostatic hyperplasia. The expressions of STAT-6 and PSA proteins were detected by immunohistochemical methods in prostate tissue. The concentration of totall PSA(tPSA) and free PSA(fPSA) in serum were detected by electrochemiluminescence. The prostate volume was measured by color doppler ultrasound. The ratio of f/ t value and prostate specific antigen density (PSAD) were calculated. RESULTS: The expressions of STAT-6 and PSA protein were significantly higher in prostatic carcinoma group (Optical Density: 0.24±0.08 and 0.31±0.09, respectively) than those in benign prostatic hyperplasia group(Optical Density: 0.12±0.06 and 0.20±0.07, respectively) (all P <0.01). The concentrations of tPSA and fPSA in serum and PSAD were significantly higher in prostatic carcinoma group [(43±26) ng/mL, (3.8± 2.2) ng/mL and (0.88±0.66) ng·mL-1·cm-3, respectively] than those in benign prostatic hyperplasia group[(6±4) ng/mL, (1.2±0.8) ng/mL and (0.12±0.09) ng·mL-1 ·cm-3, respectively] (all P <0.01). There were no statistically differences in the f/t value and prostate volume between prostatic carcinoma group[(0.14±0.10), (61±35) cm3, respectively] and benign prostatic hyperplasia group(0.31± 0.48, 47±24 cm3, respectively) (all P >0.05). CONCLUSION: STAT-6 and PSA may participate in the development of prostatic carcinoma. The concentrations of tPSA and fPSA in serum and PSAD can be applied as effective screening targets for prostatic carcinoma diagnosis.

Key words: prostatic carcinoma, signal transducer and activator of transcription, prostate specific antigen, benign prostatic hyperplasia

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