TY - JOUR
T1 - Selective microfluidic capture and detection of prostate cancer cells from urine without digital rectal examination
AU - Chan, Kit Man
AU - Gleadle, Jonathan M.
AU - Gregory, Philip A.
AU - Phillips, Caroline A.
AU - Safizadeh Shirazi, Hanieh
AU - Whiteley, Amelia
AU - Li, Jordan
AU - Vasilev, Krasimir
AU - Macgregor, Melanie
PY - 2021/11/1
Y1 - 2021/11/1
N2 - 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.
AB - 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.
KW - Biosensors
KW - Cancer detection
KW - Hexaminolevulinic acid
KW - Microfluidic
KW - Nanotechnologies
KW - Photodynamic diagnosis
KW - Prostate cancer
KW - PSMA
KW - Urine
UR - http://www.scopus.com/inward/record.url?scp=85118333441&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/FT200100301
UR - http://purl.org/au-research/grants/ARC/DP180101254
U2 - 10.3390/cancers13215544
DO - 10.3390/cancers13215544
M3 - Article
AN - SCOPUS:85118333441
SN - 2072-6694
VL - 13
JO - Cancers
JF - Cancers
IS - 21
M1 - 5544
ER -