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三尖杉酯碱通过激活 caspase-9、下调 XIAP 和 STAT-3 以及内质网应激抑制 SW872 人恶性脂肪肉瘤细胞生长并诱导其凋亡。

Growth-Suppressive and Apoptosis-Inducing Effects of Tetrandrine in SW872 Human Malignant Liposarcoma Cells via Activation of Caspase-9, Down-Regulation of XIAP and STAT-3, and ER Stress.

机构信息

Department of Molecular Medicine, College of Medicine, Keimyung University, 1095 Dalgubeoldaero, Dalseo-gu, Daegu 42601, Korea.

出版信息

Biomolecules. 2022 Jun 17;12(6):843. doi: 10.3390/biom12060843.

DOI:10.3390/biom12060843
PMID:35740967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9221093/
Abstract

Liposarcoma is a rare and heterogeneous soft tissue malignant tumor and has a significant impact on mortality with a poor prognosis. To date, there is no effective treatment for liposarcoma, whereas surgical resection is only the gold treatment with numerous adverse effects. Here we investigated whether tetrandrine inhibits the growth of SW872 human malignant liposarcoma cells. Of note, tetrandrine at 10 μM vastly inhibited growth and induced apoptosis, as evidenced by increased nuclear DNA fragmentation and sub-G1 population of SW872 cells. Mechanistically, treatment with tetrandrine led to activation of caspase-9/3 in SW872 cells, and z-VAD-fmk, a pan-caspase inhibitor, attenuated the tetrandrine-induced apoptosis and growth suppression in SW872 cells. In addition, tetrandrine treatment resulted in down-regulation of XIAP andSTAT-3 in SW872 cells, and importantly knockdown of STAT-3 caused a significant reduction of the cell survival. Tetrandrine also had abilities to up-regulate not only the expression of GRP78 and ATF-4 but also the phosphorylation of eIF-2α in SW872 cells. In summary, these results demonstrated that tetrandrine has strong growth-suppressive and apoptosis-inducing effects on SW872 cells, which are mediated through control of the intrinsic caspase pathway, down-regulation of XIAP and STAT-3, and triggering ER stress.

摘要

脂肪肉瘤是一种罕见且异质性的软组织恶性肿瘤,死亡率高,预后差。迄今为止,脂肪肉瘤尚无有效的治疗方法,而手术切除仅是金标准治疗方法,但有许多不良反应。在这里,我们研究了汉防己甲素是否能抑制 SW872 人恶性脂肪肉瘤细胞的生长。值得注意的是,汉防己甲素在 10 μM 时极大地抑制了生长并诱导了细胞凋亡,这表现为 SW872 细胞的核 DNA 片段化和亚 G1 群体增加。在机制上,汉防己甲素处理导致 SW872 细胞中 caspase-9/3 的激活,而 z-VAD-fmk,一种广谱半胱天冬酶抑制剂,减弱了汉防己甲素诱导的 SW872 细胞凋亡和生长抑制。此外,汉防己甲素处理导致 SW872 细胞中 XIAP 和 STAT-3 的下调,重要的是 STAT-3 的敲低导致细胞存活显著减少。汉防己甲素还能够上调 SW872 细胞中不仅 GRP78 和 ATF-4 的表达,而且还能上调 eIF-2α 的磷酸化。总之,这些结果表明,汉防己甲素对 SW872 细胞具有很强的生长抑制和诱导凋亡作用,这是通过控制内在的半胱天冬酶途径、下调 XIAP 和 STAT-3 以及触发内质网应激来介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/35b85c6312da/biomolecules-12-00843-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/e6264151e32b/biomolecules-12-00843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/9bca467d322f/biomolecules-12-00843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/28e5686cbf94/biomolecules-12-00843-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/349c2abf603c/biomolecules-12-00843-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/a22bbd038af4/biomolecules-12-00843-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/6f4c65edc584/biomolecules-12-00843-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/35b85c6312da/biomolecules-12-00843-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/e6264151e32b/biomolecules-12-00843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/9bca467d322f/biomolecules-12-00843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/28e5686cbf94/biomolecules-12-00843-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/349c2abf603c/biomolecules-12-00843-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/a22bbd038af4/biomolecules-12-00843-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/6f4c65edc584/biomolecules-12-00843-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ec/9221093/35b85c6312da/biomolecules-12-00843-g007.jpg

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