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Updated: Jun 11, 2025

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Isolation of Normal and Cancer-associated Fibroblasts from Fresh Tissues by Fluorescence Activated Cell Sorting FACS
Published on: January 14, 2013
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Comparative transcriptome of normal and cancer-associated fibroblasts
Apoorva Abikar1,2, Mohammad Mehaboob Subhani Mustafa1, Radhika Rajiv Athalye1
1Centre for Human Genetics, Bengaluru, India.
BMC Cancer
|October 5, 2024
Summary
Researchers identified key molecular markers in cancer-associated fibroblasts (CAFs) by comparing them to normal fibroblasts. These CAFs markers could lead to new targeted therapies to improve cancer treatment outcomes.
Area of Science:
- Oncology
- Cancer Biology
- Molecular Biology
Background:
- Tumor characteristics are influenced by the tumor micro-environment (TME).
- Cancer-associated fibroblasts (CAFs) are key cellular components of the TME, secreting factors that impact tumor growth and drug response.
- Identifying CAF-specific markers is crucial for developing novel therapeutic strategies.
Purpose of the Study:
- To identify differentially expressed genes and long non-coding RNAs (lincRNAs) between normal fibroblasts and CAFs.
- To discover potential biomarkers for targeted therapy against CAFs.
Main Methods:
- Fibroblasts were isolated from benign prostatic hyperplasia (BPH) and prostate cancer tissues.
- Transcriptome analysis was performed on RNA extracted from these fibroblasts to compare gene expression profiles.
Main Results:
- 818 differentially expressed messenger RNAs (mRNAs) and 17 lincRNAs were identified between normal and CAFs.
- 15 potential combinations of lincRNA-miRNA-mRNA were found, suggesting possible biomarkers.
Conclusions:
- The study identified distinct molecular markers in CAFs compared to normal fibroblasts.
- These markers could enable targeted therapies against CAFs or their secreted factors, potentially enhancing conventional chemotherapy.
- Further experimental validation is required to confirm these findings and their therapeutic potential.
Keywords:
Cancer-associated fibroblastsChemoresistanceLINCRNANon-coding RNAProstate cancerTumor microenvironment
