Cell Free Circulating Nucleic Acids as New Tumor Diagnostics From Human Plasma Samples.
Study Details
Study Description
Brief Summary
Cell Free Circulating Nucleic Acids as New Tumor Diagnostics From Human Plasma Samples.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Cell free circulating free nucleic acids is new substrates for laboratory diagnostics in a number of medical areas including oncology, transfusion medicine, gynecology/obstetrics, inflammatory and autoimmune diseases etc.There are various qualities of cell free nucleic acids. In oncology, it has been shown that the early detection of cell free nucleic acids originating from the tumour preceeds the diagnostic detection of clinical relapse as done by imaging techniques or clinical symptoms by 6-8- months.
Exosomes are small, lipid bilayer membrane vesicles (30-100 nm) that are released from all cell types into the extracellular space. These tiny membrane vesicles transmit EV-mediated signals by proteins, lipids, nucleic acids and sugars, and the unique molecular pattern of this package direct the type of extracellular signal to be transmitted to target cells. Interest in exosomes range from their mode of action and various functions in the body to more practical applications such as development of biomarkers based on analysis of their RNA and protein content and their use in clinical diagnostics. It was proposed that micro RNAs are transferred through exosomes to recipient cells and can there mediate repression of their mRNA targets.
The use of highly expensive targeted therapies (e.g. tyrosine kinase inhibitors or PARP inhibitors) may become obsolete during therapy due to changes in the mutational molecular profile of the malignant tumour. Indeed, if early detection of cell free nucleic acids suggest therapy failure, new stratification of the patient and changed therapy modalities may be possible in the future, thus helping to prolong overall survival of tumour patients.
Aims of the Research:
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To isolate exosomes as a stable source of cell free nucleic acids.
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To perform protein profiling on the isolated exosomes.
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To isolate nucleic acids from exosomes for analysis.
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To define and develop standards and protocols for cell free nucleic acids analysis particularly regarding epigenetic alterations with emphasis on DNA methylation.
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Optimizing of pre-analytical process to improve the pre-analytical aspects of assays.
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To test the stability of methylated compared to non-methylated circulating DNA under various pre-analytical conditions.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| case group, Melanoma Patients 15 patients of with Melanoma, Age between 40 and 90 years. -Withdrawal of Blood sample, Isolation of Exosomes: Bradford protein assay And Qubit protein assay. Bioanalyzer. Real time PCR. |
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| control group 10 Persons without Melanoma, age > 40 years -Withdrawal of Blood sample, Isolation of Exosomes: Bradford protein assay And Qubit protein assay. Bioanalyzer. Real time PCR. |
Outcome Measures
Primary Outcome Measures
- Isolation of Exosomes as a stable source of nucleic acid as an early Detection Method to diagnose Melanoma. [one year]
Real time PCR for detecting the presence of Melanoma relevant nucleic acids isolated of Exososmes.
Eligibility Criteria
Criteria
Inclusion Criteria:
- patients with Melanoma
Exclusion Criteria:
- patients with other types of malignancies
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Assiut University Hospitals- Faculty of Medicine | Assiut | Egypt | 71111 |
Sponsors and Collaborators
- Assiut University
Investigators
- Study Director: Hesham A Abdel-Baset, Prof., Assiut University- Faculty of Medicine- Clinical Pathology dept.
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Sara Alameldin 20.06.2016