Cell Free Circulating Nucleic Acids as New Tumor Diagnostics From Human Plasma Samples.

September 15, 2019 updated by: Sara Alameldin, Assiut University
Cell Free Circulating Nucleic Acids as New Tumor Diagnostics From Human Plasma Samples.

Study Overview

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:

  • To isolate exosomes as a stable source of cell free nucleic acids.
  • To perform protein profiling on the isolated exosomes.
  • To isolate nucleic acids from exosomes for analysis.
  • To define and develop standards and protocols for cell free nucleic acids analysis particularly regarding epigenetic alterations with emphasis on DNA methylation.
  • Optimizing of pre-analytical process to improve the pre-analytical aspects of assays.
  • To test the stability of methylated compared to non-methylated circulating DNA under various pre-analytical conditions.

Study Type

Observational

Enrollment (Anticipated)

15

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Assiut, Egypt, 71111
        • Recruiting
        • Assiut University Hospitals- Faculty of Medicine
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Study group: 15 Patients control Group: 10 Persons

Description

Inclusion Criteria:

  • patients with Melanoma

Exclusion Criteria:

  • patients with other types of malignancies

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
case group, Melanoma Patients

15 patients of with Melanoma, Age between 40 and 90 years.

-Withdrawal of Blood sample, Isolation of Exosomes:

  1. Bradford protein assay And Qubit protein assay.
  2. Bioanalyzer.
  3. Real time PCR.
control group

10 Persons without Melanoma, age > 40 years

-Withdrawal of Blood sample, Isolation of Exosomes:

  1. Bradford protein assay And Qubit protein assay.
  2. Bioanalyzer.
  3. Real time PCR.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Isolation of Exosomes as a stable source of nucleic acid as an early Detection Method to diagnose Melanoma.
Time Frame: one year
Real time PCR for detecting the presence of Melanoma relevant nucleic acids isolated of Exososmes.
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Hesham A Abdel-Baset, Prof., Assiut University- Faculty of Medicine- Clinical Pathology dept.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2016

Primary Completion (Anticipated)

November 1, 2019

Study Completion (Anticipated)

December 1, 2019

Study Registration Dates

First Submitted

September 5, 2019

First Submitted That Met QC Criteria

September 5, 2019

First Posted (Actual)

September 9, 2019

Study Record Updates

Last Update Posted (Actual)

September 17, 2019

Last Update Submitted That Met QC Criteria

September 15, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • Sara Alameldin 20.06.2016

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on New Tumor Diagnostics From Human Plasma Samples

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