Mechanosensitive changes in the expression of genes in colorectal cancer-associated fibroblasts.

Most solid tumors become stiff with progression of cancer. Cancer Associated Fibroblasts (CAFs), most abundant stromal cells in the tumor microenvironment (TME), are known to mediate such stiffening. While the biochemical crosstalk between CAFs and cancer cells have been widely investigated, it is not clear if and how CAFs in stiffer TME promote metastatic progression. To gather insights into the process, we controlled the mechanical stiffness of the substrates and collected gene expression data with human colorectal CAFs. We cultured human primary CAFs on 2D polyacrylamide hydrogels with increasing elastic modulus (E) of 1, 10 and 40 kPa, and performed genome-wide transcriptome analyses in these cells to identify expression levels of ~16000 genes. The high-quality RNAseq results can be an excellent data-source for bioinformatic analysis for identifying novel pathways and biomarkers in cancer development and metastatic progression. With thorough analysis and accurate interpretation, this data may help researchers understand the role of mechanical stiffness of the TME in CAF-cancer cell crosstalk. Design Type(s) solid tumor development model • biophysical progression in colorectal cancer • transcription profiling by high throughput sequencing design Measurement Type(s) transcription profiling assay Technology Type(s) RNA sequencing Factor Type(s) substrate mechanical stiffness • cancer progression stage Sample Characteristic(s) Human (Homo sapiens) • colorectal cancer (CRC)• cancer associated fibroblast [ABSTRACT FROM AUTHOR]