IGFBP-3 in Ovarian Cancer Invasion

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT00154986
Collaborator
(none)
30
1
11
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Study Details

Study Description

Brief Summary

An ovarian cancer cell line (OVTW-59) derived from an ovarian endometrioid carcinoma was established and its sublines, labeled as P0, P1, P2, P3, and P4 with increasing invasion abilities were selected from transwell invasion chambers.Using cDNA microarray and verified with quantitative reverse-transcriptase polymerase chain reaction, we have identified IGFBP-3 as an invasion-suppressor gene. We plan to study the role of IGFBP-3 in ovarian cancer invasion.

Condition or Disease Intervention/Treatment Phase
  • Procedure: immunohistochemical staining, transfection, invasion assay
N/A

Detailed Description

We have successfully established an ovarian cancer cell line (OVTW-59), which was derived from an ovarian endometrioid carcinoma. Its sublines, labeled as P0, P1, P2, P3, and P4 with increasing invasion abilities, were selected from transwell invasion chambers, where P0 represented the original cell line at 100th passage. By using cDNA microarray and verified with quantitative reverse-transcriptase polymerase chain reaction, we have identified the differentially gene expression profiles of these OVTW-59 series cell lines in order to identify the invasion related suppressor and oncogenes from ovarian carcinoma. From these genes, we selected insulin-like growth factor binding protein (IGFBP)-3, which is a suppressor gene, and found it lower expressed in higher-grade tumors and correlated with poor patient survival. In vitro, we found IGFBP-3 related to the inhibition of cancer cell migration. In this study, we plan to setup stable transfected IGFBP-3 cell lines in P0 and P4, and study the relationship among IGFBP-3, metalloproteinase-2 (our previous studies which verified its relationship with tumor invasiveness) and insulin-like growth factor (IGF)-1. We would study the changes in cytoskeletal structures and the known functions of anti-proliferation and apoptosis in IGFBP-3. Furthermore, we would like to investigate the mechanism of IGFBP-3 in the inhibition of invasion/migration of ovarian carcinoma, either signaling through MAPK or PI3K/AKT pathways. Finally, through xenograft, we plan to study for the possible application of IGFBP-3 in ovarian cancer therapy.

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
Single
Primary Purpose:
Diagnostic
Official Title:
Study of IGFBP-3 in the Ovarian Carcinoma Cell Invasion
Study Start Date :
Aug 1, 2004
Study Completion Date :
Jul 1, 2005

Outcome Measures

Primary Outcome Measures

  1. migration, invasion, metastasis []

Secondary Outcome Measures

  1. transfection efficiency []

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 80 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Ovarian Endometrioid Adenocarcinoma

Exclusion Criteria:

Other types of ovaria epithelial cell carcinoma

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwna University Hospital Taipei Taiwan 10020

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Principal Investigator: Torng Pao-Ling, MD, PhD, Department of Obsteteric and Gynecology, National Tiawan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00154986
Other Study ID Numbers:
  • 9361700500
  • NSC93-2314-B-002-168
First Posted:
Sep 12, 2005
Last Update Posted:
Sep 12, 2005
Last Verified:
Apr 1, 2004

Study Results

No Results Posted as of Sep 12, 2005