Smo gene silencing: a promising strategy for natural killer/t-cell lymphoma treatment via modulating proliferation and apoptosis.
Natural killer/T-cell lymphoma (NKTCL) is a malignancy with a poor prognosis.
APA
Liu S, Wang S, et al. (2025). Smo gene silencing: a promising strategy for natural killer/t-cell lymphoma treatment via modulating proliferation and apoptosis.. Molecular medicine (Cambridge, Mass.), 31(1), 319. https://doi.org/10.1186/s10020-025-01341-z
MLA
Liu S, et al.. "Smo gene silencing: a promising strategy for natural killer/t-cell lymphoma treatment via modulating proliferation and apoptosis.." Molecular medicine (Cambridge, Mass.), vol. 31, no. 1, 2025, pp. 319.
PMID
41162883
Abstract
Natural killer/T-cell lymphoma (NKTCL) is a malignancy with a poor prognosis. The Smoothened (Smo) protein is implicated in NKTCL growth. This study employed lentiviral vector-mediated Smo RNA interference (LV-Smo-RNAi) to silence the Smo gene in the human NKTCL cell line SNT8. Fluorescence microscopy, qRT-PCR, and Western blot verified the reduction of Smo mRNA and protein levels. The CCK-8 assay showed that Smo silencing inhibited cell proliferation. Flow cytometry with annexin V-PE/7-AAD double staining indicated an increased apoptosis rate. Moreover, the expression of GLI family zinc finger 1 (Gli1) and programmed death-ligand 1 (PD-L1) was downregulated. In vivo, xenotransplantation experiments demonstrated that Smo silencing led to slower tumor growth with reduced tumor volume and weight. Overall, Smo gene silencing holds great potential as a novel molecular-targeted therapy approach for NKTCL by effectively suppressing cell proliferation and promoting apoptosis.
MeSH Terms
Humans; Apoptosis; Cell Proliferation; Smoothened Receptor; Animals; Cell Line, Tumor; Gene Silencing; Mice; Xenograft Model Antitumor Assays; Lymphoma, T-Cell; RNA Interference; B7-H1 Antigen; Gene Expression Regulation, Neoplastic
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