不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Smo gene silencing: a promising strategy for natural killer/t-cell lymphoma treatment via modulating proliferation and apoptosis.
Smo gene silencing: a promising strategy for natural killer/t-cell lymphoma treatment via modulating proliferation and apoptosis.
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自然杀伤/T细胞淋巴瘤(NKTCL)是一种预后不良的恶性肿瘤。Smoothened(Smo)蛋白与NKTCL的生长有关。本研究采用慢病毒载体介导的Smo RNA干扰(LV-Smo-RNAi)沉默人NKTCL细胞系SNT8中的Smo基因。荧光显微镜、qRT-PCR和Western blot验证了Smo mRNA和蛋白水平的降低。CCK-8实验显示,Smo沉默抑制了细胞增殖。annexin V-PE/7-AAD双染流式细胞术表明凋亡率增加。此外,GLI家族锌指1(Gli1)和程序性死亡配体1(PD-L1)的表达下调。在体内,异种移植实验表明,Smo沉默导致肿瘤生长减慢,肿瘤体积和重量减少。总体而言,Smo基因沉默通过有效抑制细胞增殖和促进凋亡,有望成为NKTCL的一种新型分子靶向治疗方法。
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.
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