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Smo gene silencing: a promising strategy for natural killer/t-cell lymphoma treatment via modulating proliferation and apoptosis.

Molecular medicine (Cambridge, Mass.) 2025 Vol.31(1) p. 319

Liu S, Wang S, Xu Y, Huang Y, Xin P, Zheng Y, Wu Y, Yang Y, Zhu X, Li C

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Natural killer/T-cell lymphoma (NKTCL) is a malignancy with a poor prognosis.

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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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