- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05070039
Value of Cortactin Expression in Invasive and Non-invasive Urinary Bladder Urothelial Carcinoma in Egyptian Population
July 13, 2022 updated by: Maisa Hashem Mohammed, Sohag University
Urothelial carcinoma is the ninth most common malignant neoplasm worldwide.
nearly in all human tumors, actin filaments are involved in lamellopodia or cellular extensions.
Cortactin is involved in fixing the actin assembly to enhance cellular penetration.
Assessment of Cortactin expression in invasive and non-invasive urothelial carcinoma and recording any significant different expressions may have benefits in developing more effective anticancer chemotherapeutic agents.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Bladder carcinoma is the 9th most prevalent cancer worldwide.
Mostcases are diagnosed in men.
Bladder carcinoma is categorized into three disticly different categories; non- muscle invasive, muscle invasive and metastatic bladder carcinoma.
Vast majority of all bladder carcinomas are diagnosed as urothelial carcinoma (UC).
Squamous cell carcinoma (SCC), adenocarcinoma and other rare types represent the remaining 10%.
In Egypt, bladder carcinoma is ranked as the most prevalent cancer .
The most important etiological causes for such disease in Egypt are festation by S. haematopium and Cigarette smoking.
Cortactin is a 63-65 kDa protein, encoded by a gene located on 11q13.
Cortactin activates and binds to Arp2/3 and stabilizes the branched Actin networks.
Invadopodia are Actin-rich cellular protrusions, associated with enhanced proteolytic activities in the invasive regions of carcinomas. it is also incorporated in invadopodia, Cortactin expression is enhanced once or rapidly following secretions of transmembrane metalloproteinase, MT1-MMP.
Extracellular matrix (ECM) proteolytic cleavage develops soon after secretion of MT1-MMP and Cortactin.
increased secretion of Cortactin was studied in a lot of malignant tumors, including melanoma, mammary, pancreatic duct, hepatocellular and colorectal adenocarcinomas.
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
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
-
-
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Sohag, Egypt, 82524
- Maisa Hashem Mohammed
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients with primary urinary bladder carcinoma.
Exclusion Criteria:
- patients received chemotherapeutic agents.
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
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: patients with invasive and non invasive urothelial carcinoma
patients with urothelial carcinoma will be subjected to radical cystectomy or trans uretheral resection of the tumor, specimens will be sent to the pathology lab. to be examined.
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assessment of Cortactin immunohistochemical expression in invasive and non-invasive urothelial carcinoma.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment and correlating Cortactin expression in invasive and non-invasive urothelial carcinoma.
Time Frame: 6 months
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immunohistochemical staining of tumor sections and correlating the immuno-expresion of Cortactin to different tumor parameters as tumor grade, stage and status of lymph nodes involved, inorder to detect the prognostic role of Cortactin in urothelial carcinoma.
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6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
July 1, 2021
Primary Completion (Actual)
December 30, 2021
Study Completion (Actual)
January 1, 2022
Study Registration Dates
First Submitted
September 19, 2021
First Submitted That Met QC Criteria
September 27, 2021
First Posted (Actual)
October 6, 2021
Study Record Updates
Last Update Posted (Actual)
July 15, 2022
Last Update Submitted That Met QC Criteria
July 13, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Soh-Med-21-09-44
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
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