We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Stem Cell Therapy is Safe: Reprogramming Does Not Increase the Rate of Mutagenesis

By LabMedica International staff writers
Posted on 22 Feb 2017
DNA mapping studies have shown that the genomes of induced pluripotent stem cells do not contain more mutations that did the original cell line from which they were generated.

One important unsolved question in the stem cell field is, do induced pluripotent stem cells (iPSCs) have more mutations than other cultured somatic cells because of the reprogramming process? The delay in answering this question has slowed adoption of iPSCs in biomedical research and medicine, as concerns that these cells are prone to increased numbers of genetic mutations persist.

Image: Induced pluripotent stem cells (iPSCs) are the basis of a technique that opens the doors to many medical advances involving repair and restoration of tissues and organs (Photo courtesy of Darryl Leja, National Human Genome Research Institute).
Image: Induced pluripotent stem cells (iPSCs) are the basis of a technique that opens the doors to many medical advances involving repair and restoration of tissues and organs (Photo courtesy of Darryl Leja, National Human Genome Research Institute).

Investigators at the [U.S.] National Human Genome Research Institute adopted a unique approach to answering the question of the possible increase in mutation rate in iSPCs by deriving fibroblast subclones and clonal iPSC lines from the same fibroblast population. This provided the investigators with parallel cell lines from the same source, only one of which having undergone the process to turn them into iPSCs.

The investigators applied next-generation sequencing to compare genomic variations in these lines. They reported in the February 6, 2017, online edition of the journal Proceedings of the [U.S.] National Academy of Sciences that targeted deep sequencing of parental fibroblasts revealed that most variants detected in clonal iPSCs and fibroblast subclones were rare variants inherited from the parental fibroblasts. More than 90% of these mutations were random, preexisting sequence variants in small subsets of the parental fibroblast population. This data strongly suggested that reprogramming process was not mutagenic.

"This technology will eventually change how doctors treat diseases. These findings suggest that the question of safety should not impede research using iPSC," said senior author Dr. Paul Liu, senior investigator in the Translational and Functional Genomics Branch of the [U.S.] National Human Genome Research Institute.


Platinum Member
COVID-19 Rapid Test
OSOM COVID-19 Antigen Rapid Test
Magnetic Bead Separation Modules
MAG and HEATMAG
Anti-Cyclic Citrullinated Peptide Test
GPP-100 Anti-CCP Kit
New
Gold Member
TORCH Panel Rapid Test
Rapid TORCH Panel Test

Latest BioResearch News

Genome Analysis Predicts Likelihood of Neurodisability in Oxygen-Deprived Newborns

Gene Panel Predicts Disease Progession for Patients with B-cell Lymphoma

New Method Simplifies Preparation of Tumor Genomic DNA Libraries