The impact of hypoxia and oxidative stress on proteo-metabolomic alterations of 3D cholangiocarcinoma models

The three-dimensional multicellular spheroid (3D MCS) model has been employed in cholangiocarcinoma research as it generates 3D architecture and includes more physiological relevance with the multicellular arrangement. However, it is also essential to explain the molecular signature in this microenvironment and its structural complexity. The results indicated that poorly differentiated CCA cell lines were unable to form 3D MCS due to the lack of cell adhesion molecules with more mesenchymal marker expression. The well-differentiated CCA and cholangiocyte cell lines were able to develop 3D MCSs with round shapes, smooth perimeter, and cell adhesion molecules that led to the hypoxic and oxidative microenvironment detected. For MMNK-1, KKU-213C, and KKU-213A MCSs, the proteo-metabolomic analysis showed proteins and metabolic products altered compared to 2D cultures, including cell-cell adhesion molecules, energy metabolism-related enzymes and metabolites, and oxidative-related metabolites. Therefore, the 3D MCSs provide different physiological states with different phenotypic signatures compared to 2D cultures. Considering the 3D model mimics more physiological relevance, it might lead to an alternate biochemical pathway, targeting to improve drug sensitivity for CCA treatment.

Automated summary

The three-dimensional multicellular spheroid (3D MCS) model is used in cholangiocarcinoma research to mimic the physiological relevance and architecture of the tumor. The study found that poorly differentiated CCA cell lines were unable to form 3D MCS due to lack of cell adhesion molecules, while well-differentiated CCA and cholangiocyte cell lines were able to develop 3D MCSs with distinct phenotypic signatures. The 3D MCSs provide a different physiological state compared to 2D cultures, making it a valuable tool for studying drug sensitivity and alternate biochemical pathways.