BACKGROUND: Multiplex urine-based assay emerged outperforms single biomarker (e.g., prostate-specific antigen, PSA) for predicting prostate cancer (CaP), whereas its combined mode has to be fully optimized. Our aim is to determine whether a strategy of combining gene-based, protein-based, metabolite-based with positive, negative makers in urine could optimize a multiplex model for detecting CaP. METHODS: Using quantitative PCR, Western blot, and liquid chromatography-mass spectrometry, expression patterns of PCA3, TMPRSS2: ERG, Annexin A3, Sarcosine, and urine PSA were evaluated in urine samples from 86 untreated patients with CaP and 45 patients with no evidence of malignancy. Multivariate logistic regression analysis was used to generate a final model and receiver-operating characteristic (ROC) analysis and special bootstrap software to assess diagnostic performance of tested variables. RESULTS: The expression patterns of PCA3, TMPRSS2: ERG, Annexin A3, Sarcosine, and a panel including these biomarkers were significant predictors of CaP both in patients with PSA 4-10 ng/ml and in all patients (all P < 0.05). Employing ROC analysis, the area under the curves of the panel in these both cohorts were 0.840 and 0.856, respectively, which outperform that of any single biomarker (PCA3: 0.733 and 0.739; TMPRSS2: ERG: 0.720 and 0.732; Annexin A3: 0.716 and 0.728; Sarcosine: 0.659 and 0.665, respectively). CONCLUSIONS: Compared with single biomarker, the multiplex model including PCA3, TMPRSS2: ERG, Annexin A3 and Sarcosine adds even more to the diagnostic performance for predicting CaP. Further validation experiments and optimization for the strategy of constructing this model are warranted.
BACKGROUND: Multiplex urine-based assay emerged outperforms single biomarker (e.g., prostate-specific antigen, PSA) for predicting prostate cancer (CaP), whereas its combined mode has to be fully optimized. Our aim is to determine whether a strategy of combining gene-based, protein-based, metabolite-based with positive, negative makers in urine could optimize a multiplex model for detecting CaP. METHODS: Using quantitative PCR, Western blot, and liquid chromatography-mass spectrometry, expression patterns of PCA3, TMPRSS2: ERG, Annexin A3, Sarcosine, and urine PSA were evaluated in urine samples from 86 untreated patients with CaP and 45 patients with no evidence of malignancy. Multivariate logistic regression analysis was used to generate a final model and receiver-operating characteristic (ROC) analysis and special bootstrap software to assess diagnostic performance of tested variables. RESULTS: The expression patterns of PCA3, TMPRSS2: ERG, Annexin A3, Sarcosine, and a panel including these biomarkers were significant predictors of CaP both in patients with PSA 4-10 ng/ml and in all patients (all P < 0.05). Employing ROC analysis, the area under the curves of the panel in these both cohorts were 0.840 and 0.856, respectively, which outperform that of any single biomarker (PCA3: 0.733 and 0.739; TMPRSS2: ERG: 0.720 and 0.732; Annexin A3: 0.716 and 0.728; Sarcosine: 0.659 and 0.665, respectively). CONCLUSIONS: Compared with single biomarker, the multiplex model including PCA3, TMPRSS2: ERG, Annexin A3 and Sarcosine adds even more to the diagnostic performance for predicting CaP. Further validation experiments and optimization for the strategy of constructing this model are warranted.
Authors: Yuanyuan Liang; Jamie C Messer; Christopher Louden; Miguel A Jimenez-Rios; Ian M Thompson; Hector R Camarena-Reynoso Journal: Urol Oncol Date: 2012-02-03 Impact factor: 3.498
Authors: Yuanyuan Liang; Donna P Ankerst; Ziding Feng; Rong Fu; Janet L Stanford; Ian M Thompson Journal: Urol Oncol Date: 2012-05-01 Impact factor: 3.498
Authors: Stella Koutros; Tamra E Meyer; Stephen D Fox; Haleem J Issaq; Timothy D Veenstra; Wen-Yi Huang; Kai Yu; Demetrius Albanes; Lisa W Chu; Gerald Andriole; Robert N Hoover; Ann W Hsing; Sonja I Berndt Journal: Carcinogenesis Date: 2013-05-22 Impact factor: 4.944
Authors: Amjad P Khan; Thekkelnaycke M Rajendiran; Bushra Ateeq; Irfan A Asangani; Jyoti N Athanikar; Anastasia K Yocum; Rohit Mehra; Javed Siddiqui; Ganesh Palapattu; John T Wei; George Michailidis; Arun Sreekumar; Arul M Chinnaiyan Journal: Neoplasia Date: 2013-05 Impact factor: 5.715