High-content siRNA 3D co-cultures to identify myoepithelial cell-derived breast cancer suppressor proteins.
Hendrika M DuivenvoordenNatasha K BrockwellCameron J NowellKaylene J SimpsonBelinda S ParkerPublished in: Scientific data (2021)
Understanding how cancer cells interact with the surrounding microenvironment early in breast cancer development can provide insight into the initiation and progression of invasive breast cancers. The myoepithelial cell layer surrounding breast ducts acts as a physical barrier in early breast cancer, preventing cancer cells from invading the surrounding stroma. Changes to the expression profile and properties of myoepithelial cells have been implicated in progression to invasive carcinoma. Identifying the molecular drivers of myoepithelial cell-mediated tumour suppression may offer new approaches to predict and block the earliest stages of cancer invasion. We employed a high-content approach to knock down 87 different genes using siRNA in an immortalised myoepithelial cell line, prior to co-culture with invasive breast cancer cells in 3D. Combined with high-content imaging and a customised analysis pipeline, this system was used to identify myoepithelial proteins that are necessary to control cancer cell invasion. This dataset has identified prospective myoepithelial suppressors of early breast cancer invasion which may be used by researchers to investigate their clinical validity and utility.
Keyphrases
- early breast cancer
- papillary thyroid
- squamous cell
- breast cancer cells
- single cell
- stem cells
- induced apoptosis
- cancer therapy
- cell therapy
- physical activity
- high resolution
- squamous cell carcinoma
- signaling pathway
- cell cycle arrest
- genome wide
- mass spectrometry
- bone marrow
- drug delivery
- dna methylation
- endoplasmic reticulum stress
- pi k akt
- genome wide analysis