Trials / Completed
CompletedNCT00953693
Patient Specific Induced Pluripotency Stem Cells (PSiPS)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 15 (estimated)
- Sponsor
- Royan Institute · Other Government
- Sex
- All
- Age
- 12 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
Induced pluripotent stem cells (iPSCs) are adult cells that have been genetically reprogrammed to an embryonic stem cell-like state by being forced to express genes and factors important for maintaining the defining properties of embryonic stem cells. The reprogramming of adult cells into embryonic stem (ES) cells enables the generation of patient-specific stem cells and thus has enormous potential for the treatment and analysis of degenerative diseases. In this project the investigators are going to induce pluripotent stem cells from cell cultures from skin biopsies of patients. The iPS cells will be developed for modeling diseases and drug discovery as well as basic research.
Detailed description
iPS cells are typically derived by transfection of certain stem cell-associated genes into non-pluripotent cells, such as adult fibroblasts. Transfection is typically achieved through viral vectors, such as retroviruses. Transfected genes include the master transcriptional regulators Oct-3/4 (Pouf51) and Sox2, although to enhance the efficiency of induction some other genes e.g. Klf4, c-Myc. In this study after separation the fibroblasts from patient's skin biopsy, the cells are transfected with 4 Yamanaka factors (human Oct4, Sox2, Klf4, c-Myc) after 3-4 weeks, transfected cells are isolated through morphological selection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Biopsy | Skin biopsy |
Timeline
- Start date
- 2009-04-01
- Primary completion
- 2010-01-01
- Completion
- 2010-07-01
- First posted
- 2009-08-06
- Last updated
- 2012-12-27
Locations
1 site across 1 country: Iran
Source: ClinicalTrials.gov record NCT00953693. Inclusion in this directory is not an endorsement.