Selective Microfluidic Capture and Detection of Prostate Cancer Cells from Urine without Digital Rectal Examination.
Kit Man ChanJonathan M GleadlePhilip A GregoryCaroline A PhillipsHanieh Safizadeh ShiraziAmelia WhiteleyJordan LiKrasimir A VasilevMelanie N MacGregorPublished in: Cancers (2021)
Urine-based biomarkers have shown suitable diagnostic potential for prostate cancer (PCa) detection. Yet, until now, prostatic massage remains required prior to urine sampling. Here, we test a potential diagnostic approach using voided urine collected without prior digital rectal examination (DRE). In this study, we evaluated the diagnostic performance of a microfluidic-based platform that combines the principle of photodynamic diagnostic with immunocapture for the detection of PCa cells. The functionality and sensitivity of this platform were validated using both cultured cells and PCa patient urine samples. Quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR) demonstrated this platform had a detection limit of fewer than 10 cells per 60 µL and successfully validated the presence of a PCa biomarker in the urine of cancer patients without prior DRE. This biosensing platform exhibits a sensitivity of 72.4% and a specificity of 71.4%, in suitable agreement with qRT-PCR data. The results of this study constitute a stepping stone in the future development of noninvasive prostate cancer diagnostic technologies that do not require DRE.
Keyphrases
- prostate cancer
- induced apoptosis
- label free
- high throughput
- real time pcr
- cell cycle arrest
- loop mediated isothermal amplification
- radical prostatectomy
- signaling pathway
- endoplasmic reticulum stress
- oxidative stress
- high resolution
- human health
- quantum dots
- benign prostatic hyperplasia
- artificial intelligence
- data analysis