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SRVF,一种包含玄参和钩藤的新型草药配方,破坏焦点黏附,并导致恶性癌细胞发生分离诱导凋亡。

SRVF, a novel herbal formula including Scrophulariae Radix and Viticis Fructus, disrupts focal adhesion and causes detachment-induced apoptosis in malignant cancer cells.

机构信息

Korean Medicine (KM) Application Center, Korea Institute of Oriental Medicine (KIOM), 70 Chumdan-ro, Dong-gu, Daegu, 41062, Republic of Korea.

出版信息

Sci Rep. 2017 Oct 16;7(1):12756. doi: 10.1038/s41598-017-12934-y.

DOI:10.1038/s41598-017-12934-y
PMID:29038437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5643381/
Abstract

When cells lose adhesion, they undergo detachment-induced apoptosis, known as anoikis. In contrast, tumor cells acquire resistance to anoikis, enabling them to survive, even after separating from neighboring cells or the ECM. Therefore, agents that restore anoikis sensitivity may serve as anti-cancer candidates. In this study, we constructed a novel herbal formula, SRVF, which contains Scrophulariae Radix (SR) and Viticis Fructus (VF). SRVF rapidly decreased cell adhesion, altered the cell morphology to round, and induced cell death; however, SR, VF, or their co-treatment did not. SRVF arrested HT1080 cells in G/M phase, increased the levels of pro-apoptotic proteins, and decreased the levels of anti-apoptotic proteins. Furthermore, SRVF efficiently reduced cell-cell and cell-ECM interactions by disrupting the F-actin cytoskeleton and down-regulating the levels of focal adhesion-related proteins, suggesting that SRVF efficiently triggers detachment-induced apoptosis (i.e., anoikis) in malignant cancer cells. In xenograft mouse models, daily oral administration of 50 or 100 mg/kg SRVF retarded tumor growth in vivo, and repeated administration of SRVF did not cause systemic toxicity in normal mice. These data collectively indicate that SRVF induces cancer cell death by restoring anoikis sensitivity via disrupting focal adhesion. Therefore, SRVF may be a safe and potent anti-cancer herbal decoction.

摘要

当细胞失去黏附力时,它们会经历脱落诱导的凋亡,称为失巢凋亡。相比之下,肿瘤细胞获得了对失巢凋亡的抗性,使它们能够在与邻近细胞或细胞外基质分离后存活。因此,恢复失巢凋亡敏感性的药物可能成为抗癌候选药物。在这项研究中,我们构建了一种新型草药配方 SRVF,它包含玄参(SR)和络石藤(VF)。SRVF 可迅速降低细胞黏附力,使细胞形态变为圆形,并诱导细胞死亡;然而,SR、VF 或它们的联合处理并没有这种作用。SRVF 将 HT1080 细胞阻滞在 G2/M 期,增加促凋亡蛋白的水平,并降低抗凋亡蛋白的水平。此外,SRVF 通过破坏 F-肌动蛋白细胞骨架和下调与黏附斑相关的蛋白水平,有效地减少细胞-细胞和细胞-细胞外基质的相互作用,表明 SRVF 有效地触发了恶性癌细胞的脱落诱导凋亡(即失巢凋亡)。在异种移植小鼠模型中,每天口服 50 或 100mg/kg 的 SRVF 可在体内延缓肿瘤生长,并且重复给予 SRVF 不会在正常小鼠中引起全身毒性。这些数据表明,SRVF 通过破坏黏附斑来恢复失巢凋亡敏感性从而诱导癌细胞死亡。因此,SRVF 可能是一种安全有效的抗癌草药方剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/d88ac39f7e43/41598_2017_12934_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/59b4f39b6d6f/41598_2017_12934_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/11e76dafffd8/41598_2017_12934_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/281b631025e4/41598_2017_12934_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/7d3230151efe/41598_2017_12934_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/e688ad31ef37/41598_2017_12934_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/9cda5490f00c/41598_2017_12934_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/1f102c3a5a93/41598_2017_12934_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/d88ac39f7e43/41598_2017_12934_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/59b4f39b6d6f/41598_2017_12934_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/11e76dafffd8/41598_2017_12934_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/281b631025e4/41598_2017_12934_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/7d3230151efe/41598_2017_12934_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/e688ad31ef37/41598_2017_12934_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/9cda5490f00c/41598_2017_12934_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/1f102c3a5a93/41598_2017_12934_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/5643381/d88ac39f7e43/41598_2017_12934_Fig8_HTML.jpg

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