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Updated: Mar 8, 2026

Generation of Induced Pluripotent Stem Cells from Human Melanoma Tumor-infiltrating Lymphocytes
Published on: November 11, 2016
Piwil2-transfected human fibroblasts are cancer stem cell-like and genetically unstable
Deying Zhang1, Xin Wu1, Xing Liu1
1Department of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Chongqing 400014, China.
Abstract:
Uncontrolled cell proliferation and inhibition of apoptosis are considered to be vital for cancer initiation, maintenance, infiltration, metastasis and recurrence after anti-cancer therapy. Here we report the generation of a novel cell line by reprogramming child foreskin fibroblast with the full length apoptosis inhibitor gene PIWIL2. The fibroblasts transfected with PIWIL2 expressed the stem cell markers OCT-4, NANOG, SOX-2, KLF-4 and C-MYC; endoderm marker AFP and GATA6; mesoderm markers ACTA2 and BRACHYURY; and ectoderm markers NESTIN and TUBB3. The karyotype was found to be hyperdiploid. The PIWIL2 transfected fibroblast cells grew into tumorous masses within 5 weeks of subcutaneous injection into adult nude mice. Although the injected cell expressed markers for all three germlines, ectoderm, mesoderm, and endoderm, they did not form teratomas in vivo. This study indicates that the PIWIL2 gene could play a key role in cancer induction and maintenance. This method for generating induced tumorigenic cells (ITGC) provides a new research tool to study oncogenesis that in turn may lead to a better understanding of cancer etiology and the development of novel anti-cancer therapies.
Insights
Researchers reprogrammed child fibroblasts using the apoptosis inhibitor gene PIWIL2, creating induced tumorigenic cells (ITGC). These cells promote cancer development, offering a new tool for oncogenesis research and potential therapeutic strategies.
Area of Science:
- Oncology
- Stem Cell Biology
- Gene Therapy
Background:
- Uncontrolled cell proliferation and apoptosis inhibition are critical in cancer development and recurrence.
- The PIWIL2 gene's role in cancer initiation and maintenance requires further investigation.
Purpose of the Study:
- To generate a novel cell line by reprogramming fibroblasts with the PIWIL2 gene.
- To investigate the potential of PIWIL2 in inducing tumorigenicity and its implications for cancer research.
Main Methods:
- Reprogramming of child foreskin fibroblasts using the full-length PIWIL2 gene.
- Characterization of transfected cells for stem cell and germline markers (OCT-4, NANOG, SOX-2, KLF-4, C-MYC, AFP, GATA6, ACTA2, BRACHYURY, NESTIN, TUBB3).
- In vivo tumorigenicity assay via subcutaneous injection into nude mice.
Main Results:
- PIWIL2-transfected fibroblasts expressed pluripotency and germline markers.
- The cells exhibited hyperdiploid karyotype.
- Subcutaneous injection led to tumor formation within 5 weeks, but not teratomas.
- The study identified PIWIL2 as a potential cancer induction and maintenance gene.
Conclusions:
- The PIWIL2 gene may play a significant role in cancer induction and maintenance.
- The generation of induced tumorigenic cells (ITGC) provides a novel research model for studying oncogenesis.
- This approach could advance understanding of cancer etiology and the development of new anti-cancer therapies.
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