Engineered Bacteriorhodopsin May Induce Lung Cancer Cell Cycle Arrest and Suppress Their Proliferation and Migration.
Chui-Wei WongLing-Ning KoHung-Jin HuangChii-Shen YangShan-Hui HsuPublished in: Molecules (Basel, Switzerland) (2021)
Highly expressible bacteriorhodopsin (HEBR) is a light-triggered protein (optogenetic protein) that has seven transmembrane regions with retinal bound as their chromophore to sense light. HEBR has controllable photochemical properties and regulates activity on proton pumping. In this study, we generated HEBR protein and incubated with lung cancer cell lines (A549 and H1299) to evaluate if there was a growth-inhibitory effect with or without light illumination. The data revealed that the HEBR protein suppressed cell proliferation and induced the G0/G1 cell cycle arrest without light illumination. Moreover, the migration abilities of A549 and H1299 cells were reduced by ~17% and ~31% after incubation with HEBR (40 μg/mL) for 4 h. The Snail-1 gene expression level of the A549 cells was significantly downregulated by ~50% after the treatment of HEBR. In addition, HEBR significantly inhibited the gene expression of Sox-2 and Oct-4 in H1299 cells. These results suggested that the HEBR protein may inhibit cell proliferation and cell cycle progression of lung cancer cells, reduce their migration activity, and suppress some stemness-related genes. These findings also suggested the potential of HEBR protein to regulate the growth and migration of tumor cells, which may offer the possibility for an anticancer drug.
Keyphrases
- cell cycle arrest
- pi k akt
- cell proliferation
- cell death
- gene expression
- cell cycle
- induced apoptosis
- protein protein
- amino acid
- stem cells
- signaling pathway
- binding protein
- epithelial mesenchymal transition
- optical coherence tomography
- risk assessment
- big data
- single cell
- diabetic retinopathy
- deep learning
- replacement therapy
- smoking cessation
- stress induced
- endoplasmic reticulum stress
- diabetic rats