Synthetic Metabolic and Genetic Networks for Medical Diagnosics
- Conditions
- ProstateCancer
- Interventions
- Other: Blood sample (1 EDTA tube, 1 SST tube, 1 Streck tube) and urine sample (100 ml)
- Registration Number
- NCT04518072
- Lead Sponsor
- University Hospital, Montpellier
- Brief Summary
This is a category 3 human study, prospective, comparative, in parallel groups. A comparative qualitative and quantitative analysis of several markers in 250 samples is proposed.
- Detailed Description
The assumption is that researchers can engineer synthetic metabolic and genetic networks to expand the panel of molecules that are currently known to be detected by natural systems. The investigators also hypothesize synthetic metabolic and genetic networks can be tuned for decisions making and in particular to diagnose diseases from biomarkers detections.
This project proposes for the first time a hybrid analogue / digital solution for the multiplexed detection of biomarkers using bacterial and paper-based biosensors. Biosensors can be designed using analog or digital devices. Digital devices in synthetic and natural systems are noise-resistant and useful for decision-making. Analog devices are useful for signal transmission and processing. Here the investigators take advantage of signal transmission and processing via analog transducers and adders, and then decision-making via genetic switches. Such a hybrid analogue / digital approach has not yet been developed for biosensing. Another novelty of the project is to use synthetic metabolic pathways to develop analog devices. The advantage in term of treatment, for example, consists in the fact that the speed of enzymatic reactions in an analog adder far exceeds the speed of gene expression required to create a genetic logic matrix; it becomes even more pronounced when the devices are connected in series. The methodology will be illustrated for the detection of biomarkers of prostate tumors, but it is broad enough to be applicable to other diagnoses. The choice to develop biosensors for prostate disease is of practical relevance since the current screening strategy (based on PSA measurement) can lead to overdiagnosis and cannot differentiate between patients with aggressive tumors and those with an indolent illness.This study propose to mainly develop a bacterial and paper-based biosensor system
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Male
- Target Recruitment
- 250
- Men aged over 18
- Informed, written consent of the patient for the biological collection
- Subject affiliated to a French social security scheme or beneficiary of such a scheme
Patients specific inclusion criteria :
- Admitted to care prostate disease or suspicion of prostate cancer and with a positive or negative PSA blood result
Controls specific inclusion criteria :
- Man free from all prostate or bladder pathologies
- Patient under legal protection
- Persons deprived of their liberty, protected adults or vulnerable persons
- Participants may withdraw their consent at any time and for any reason whatsoever without incurring any negative consequences without change in their usual care
Controls specific non-inclusion criteria :
- Patient with current prostatic or urinary infection
- History of treatment for prostate cancer other than surveillance management
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Biopsy prostatic group Blood sample (1 EDTA tube, 1 SST tube, 1 Streck tube) and urine sample (100 ml) positive biopsy (100) negative biopsy (100) Control group Blood sample (1 EDTA tube, 1 SST tube, 1 Streck tube) and urine sample (100 ml) No prostate cancer (50)
- Primary Outcome Measures
Name Time Method Ability to detect and quantify biomarkers such as PSA in samples using biosensors platform Up to 69 months The positive signal is bases on a permeation in E. coli cell membrane and recombinase switches.
- Secondary Outcome Measures
Name Time Method Investigational biomarker panel for diagnosis / Creatinine Baseline Biospecimen retention: blood serum and urine (unit µmol/l)
Investigational biomarker panel for diagnosis / Fumarate Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / Putrescine Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / 2-oxoglutarate Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / Sarcosine Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / Ornithine Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / Serotonin Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / inositol Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / Prostatic specific antigen Baseline Biospecimen retention: blood serum and urine (unit mg/l)
Investigational biomarker panel for diagnosis / Choline Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis / Spermine Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis /ribitol Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis /Taurine Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Investigational biomarker panel for diagnosis /citrate Baseline Biospecimen retention: blood serum and urine (unit: mg/l)
Trial Locations
- Locations (2)
Clinique Beau Soleil
🇫🇷Montpellier, France
University Hospital
🇫🇷Montpellier, Hérault, France