The Expression of CD24 "do-not-eat-me" Signal in Cholangiocarcinoma
CD24CCA
2 other identifiers
observational
50
1 country
1
Brief Summary
The investigators found an inverse relationship between CD24 and MiR-122 levels. Then the investigators found that CD24 that goes up with MiR-122 down makes macrophages unable to engulf the tumor cells. All this in mice. the investigators are interested in confirming this result in humans. Details of the preliminary results are attached to the submission of the research documents. the investigators will compare Cholangiocarcinoma tumors with other solid tumors, including liver tissue. The need to deepen understanding the investigators will also make a comparison between cancerous tissue and "normal" tissue adjacent to the tumor.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2023
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 10, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2024
CompletedFirst Submitted
Initial submission to the registry
November 10, 2024
CompletedFirst Posted
Study publicly available on registry
November 27, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
October 28, 2026
ExpectedMarch 14, 2025
October 1, 2024
12 months
November 10, 2024
March 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
the investigators will analyze ductular reaction and cancer stem cells markers including CD24, CD44
the investigators will perform the analysis on tissue samples of cholangiocarcinoma and non tumor controls, using immunohistochemistry and RT-PCR
All along the study, from the first recruitment to the last recruitment. average of 1 year
Eligibility Criteria
Patients with liver cancer.
You may qualify if:
- \* Donors with cholangiocarcinoma samples
You may not qualify if:
- \* Donors who do not have cholangiocarcinoma samples
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hdassah Hospital
Jerusalem, Israel, 9112001, Israel
Biospecimen
the investigators are collecting plasma circulating free DNA. the investigators are not performing DNA sequencing. this is similar to chipSEQ.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Tamar Hamburger
Hadassah Hospital Hebrew University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 10, 2024
First Posted
November 27, 2024
Study Start
November 10, 2023
Primary Completion
November 1, 2024
Study Completion (Estimated)
October 28, 2026
Last Updated
March 14, 2025
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- January 2028 for 7 years
- Access Criteria
- After publication any one.
Publication