Resumen
The colony formation assay (CFA) is a widely used method to assess the self-renewal capacity of cancer cells and evaluate how this property is affected by drug treatment. This protocol presents a streamlined, high-throughput CFA workflow optimized for T-cell acute lymphoblastic leukemia (T-ALL), making it suitable for large-scale drug screening projects. Colonies are grown in a methylcellulose-based 3D matrix and quantified using an automated analysis pipeline, allowing robust estimation of colony number and size. This cost-effective approach provides a scalable platform for identifying compounds that impair self-renewal, facilitating prioritization of hits for validation in more complex in vivo models.
| Idioma original | English |
|---|---|
| Número de artículo | 103757 |
| Publicación | Stem Cell Research |
| Volumen | 87 |
| DOI | |
| Estado | Published - sept 2025 |
Nota bibliográfica
Publisher Copyright:© 2025 The Authors
Financiación
This research was supported by the National Cancer Institute ( R37CA227656 to JSB) and the Kentucky Pediatric Cancer Research Trust Fund ( PON2 728 2400001524 to JSB).
| Financiadores | Número del financiador |
|---|---|
| National Childhood Cancer Registry – National Cancer Institute | R37CA227656 |
| Kentucky Pediatric Cancer Research Trust Fund | PON2 728 2400001524 |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
-
Good health and well being
ASJC Scopus subject areas
- General Medicine
- Developmental Biology
- Cell Biology
Huella
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