KANSL2 and MBNL3 are regulators of pancreatic ductal adenocarcinoma invasion.
Peter O OladimejiJesse BakkeWilliam C WrightTaosheng ChenPublished in: Scientific reports (2020)
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal forms of cancer. One major reason for this is that PDAC quickly metastasizes to other organs, thereby making its treatment difficult. The molecular machinery driving PDAC metastasis is still poorly understood. In this study, we applied an unbiased approach using CRISPR screening to identify genes that strongly regulate invasion (based on an in vitro assessment of their metastatic potential) in PANC-1, a PDAC cell line. Through CRISPR screening, we identified MBNL3 and KANSL2 as strong regulators of invasion in PANC-1 cells. We further validated MBNL3 and KANSL2 as regulators of PANC-1 cell invasion by using the doxycycline-inducible shRNA system. We also showed that MBNL3 and KANSL2 do not affect cell proliferation. Through our efforts, we have established a process to identify genes that regulate cell invasion and can be further investigated as potential targets for therapeutic intervention.
Keyphrases
- genome wide
- cell migration
- cell proliferation
- transcription factor
- crispr cas
- genome editing
- dna methylation
- induced apoptosis
- randomized controlled trial
- small cell lung cancer
- squamous cell carcinoma
- genome wide identification
- papillary thyroid
- bioinformatics analysis
- gene expression
- cell cycle
- quality improvement
- mass spectrometry
- endoplasmic reticulum stress
- signaling pathway
- high resolution
- cell death
- combination therapy
- genome wide analysis
- replacement therapy
- childhood cancer