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来自绵毛酸模叶蓼的倍半萜破坏线粒体膜电位以诱导细胞凋亡,并通过下调NCI-H460细胞中的基质金属蛋白酶和骨桥蛋白来抑制转移。

Sesquiterpene from Polygonum barbatum disrupts mitochondrial membrane potential to induce apoptosis and inhibits metastasis by downregulating matrix metalloproteinase and osteopontin in NCI-H460 cells.

作者信息

Zehra Binte, Ahmed Ayaz, Khan Ajmal, Shams Afshan, Uddin Reaz, Rafi Sidra, Khan Taseer Ahmed, Farooq Umar, Abid Ali Syed

机构信息

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan.

Natural and Medical Sciences Research Center, University of Nizwa, Postal Code 616, Birkat Al Mauz, P.O. Box 33, Nizwa, Sultanate of Oman.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2022 Aug;395(8):987-1001. doi: 10.1007/s00210-022-02256-w. Epub 2022 May 23.

Abstract

Globally, lung cancer accounts for 18% of cancer-associated mortalities. Among the subtypes, non-small cell lung cancer (NSCLC) is the most prevalent. The increased resistance and poor survival rates signify disease aggressiveness and thus require a search for an alternative anticancer molecule. Earlier, the sesquiterpene, i.e., compound 3 ((E)-methyl 6-acetoxy-7-methoxy-1-(2-methylpropylidene)-1H-indene-3-carboxylate) from Polygonum barbatum, was isolated, characterized by us, and reported for preliminary anticancer activity. Therefore, based on these results, this study was designed to explore the underlying molecular mechanism of apoptosis and metastasis against NCI-H460 cells. The molecular mechanism of compound 3 inducing apoptosis and inhibiting metastasis was elucidated by analyzing mitochondrial membrane potential, DNA fragmentation, clonogenic assay, invasion assay, and expression of apoptotic (caspases 3, 6, 8, 9, and BAK) and metastatic markers (MMP 2, MMP 9, and osteopontin). Compound 3 significantly inhibited cell proliferation and induced apoptosis via the intrinsic route, i.e., the mitochondrial pathway, by disrupting mitochondrial membrane potential. The enhanced expression of caspases 6, 9, BAK, and HRK with downregulation of Bcl-2L1 and Ki67 further confirmed the involvement of the intrinsic apoptotic pathway. Moreover, compound 3 restricted the invasive nature of NCI-H460 cells evinced by reduced cell invasion in Boyden chamber invasion assay and downregulating the expression of metastatic markers, i.e., matrix metalloproteinase 2/9 and VEGF. It was also found to block osteopontin by negatively regulating its expression, a marker protein in cancer management. Conclusively, this sesquiterpene exhibited potent anticancer and antimetastatic activity and can be explored further as possible pharmacophores.

摘要

在全球范围内,肺癌占癌症相关死亡人数的18%。在这些亚型中,非小细胞肺癌(NSCLC)最为常见。耐药性增加和生存率低下表明该疾病具有侵袭性,因此需要寻找替代的抗癌分子。早些时候,我们从杠板归中分离出倍半萜,即化合物3((E)-6-乙酰氧基-7-甲氧基-1-(2-甲基亚丙基)-1H-茚-3-羧酸甲酯),对其进行了表征,并报道了其初步抗癌活性。因此,基于这些结果,本研究旨在探索其针对NCI-H460细胞的凋亡和转移的潜在分子机制。通过分析线粒体膜电位、DNA片段化、克隆形成试验、侵袭试验以及凋亡(半胱天冬酶3、6、8、9和BAK)和转移标志物(基质金属蛋白酶2、基质金属蛋白酶9和骨桥蛋白)的表达,阐明了化合物3诱导凋亡和抑制转移的分子机制。化合物3通过破坏线粒体膜电位,显著抑制细胞增殖并通过内在途径(即线粒体途径)诱导凋亡。半胱天冬酶6、9、BAK和HRK的表达增强以及Bcl-2L1和Ki67的下调进一步证实了内在凋亡途径的参与。此外,在Boyden小室侵袭试验中,化合物3降低了细胞侵袭,并下调了转移标志物(即基质金属蛋白酶2/9和血管内皮生长因子)的表达,从而限制了NCI-H460细胞的侵袭性。还发现它通过负调节骨桥蛋白的表达来阻断骨桥蛋白,骨桥蛋白是癌症治疗中的一种标志物蛋白。总之,这种倍半萜表现出强大的抗癌和抗转移活性,可以作为可能的药效基团进一步探索。

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