Cytotoxic Effect of a β1,4-Galactosyltransferase Inhibitor in Hepatic Carcinoma Cells.
The incidence and mortality of hepatocellular carcinoma (HCC) are increasing worldwide, underscoring the need for novel therapeutic strategies.
APA
Dai Z, Sun M, et al. (2026). Cytotoxic Effect of a β1,4-Galactosyltransferase Inhibitor in Hepatic Carcinoma Cells.. Cells, 15(3). https://doi.org/10.3390/cells15030251
MLA
Dai Z, et al.. "Cytotoxic Effect of a β1,4-Galactosyltransferase Inhibitor in Hepatic Carcinoma Cells.." Cells, vol. 15, no. 3, 2026.
PMID
41677617
Abstract
The incidence and mortality of hepatocellular carcinoma (HCC) are increasing worldwide, underscoring the need for novel therapeutic strategies. Synthetic 2-naphthyl 2-butanamido-2-deoxy-1-thio-β-d-glucopyranoside () is a selective inhibitor of β1,4-galactosyltransferase 1 (β4GalT1). In this study, we investigated the cytotoxic effects of across multiple cancer cell lines, with a focus on HCC, and explored the underlying mechanisms. We demonstrate that preferentially exhibits cytotoxicity toward cancer cells with elevated expression of β4GalT family members, while human umbilical vein endothelial cells and immortalized human embryonic kidney epithelial cells are comparatively less sensitive. Treatment with suppresses cancer cell migration and invasion and induces pronounced endoplasmic reticulum and Golgi stress, accompanied by G2/M cell cycle arrest. Furthermore, activates apoptosis through ER stress-associated pathways by downregulating the anti-apoptotic protein Bcl-2 and upregulating pro-apoptotic proteins Bax and Bak, along with activation of caspase-3, -8, and -9. Collectively, these findings identify as a promising anti-cancer candidate targeting β4GalTs-overexpressing HCC cells and warrant further therapeutic development.
MeSH Terms
Humans; Carcinoma, Hepatocellular; Liver Neoplasms; Apoptosis; Endoplasmic Reticulum Stress; Cell Line, Tumor; Cell Movement; Enzyme Inhibitors; Galactosyltransferases; Human Umbilical Vein Endothelial Cells; G2 Phase Cell Cycle Checkpoints; Cell Proliferation; Antineoplastic Agents
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