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Suppressing migration and invasion of H1299 lung cancer cells by honokiol through disrupting expression of an HDAC6‐mediated matrix metalloproteinase 9

机译:通过破坏HDAC6介导的基质金属蛋白酶9的表达抑制H1299肺癌细胞的迁移和侵袭。

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Metastasis is the crucial mechanism to cause high mortality in lung cancer. Degradation of extracellular matrix (ECM) by proteolytic enzymes, especially matrix metalloproteinases (MMPs), is a key process for promoting cancer cell migration and invasion. Therefore, targeting MMPs might be a strategy for lung cancer metastasis suppression. Honokiol, a biological active component of Magnolia officinalis, has been indicated to suppress lung cancer tumorigenesis through epigenetic regulation. However, the regulation of MMPs‐mediated migration and invasion by honokiol through epigenetic regulation in lung cancer is still a mystery. In the present study, the migration and invasion ability of H1299 lung cancer was suppressed by noncytotoxic concentrations of honokiol treatment. The proteolytic activity of MMP‐9, rather than MMP‐2, was inhibited in honokiol‐treated H1299 cells. Honokiol‐inhibited MMP‐9 expression was through promoting MMP‐9 protein degradation rather than suppressing transcription mechanism. Furthermore, the expression of specific histone deacetylases 6 (HDAC6) substrate, acetyl‐α‐tubulin, was accumulated after honokiol incubation. The disassociation of MMP‐9 with hyper‐acetylated heat shock protein 90 (Hsp90) was observed resulting in MMP‐9 degradation after honokiol treatment. Meanwhile, honokiol‐suppressed MMP‐9 expression and invasion ability of H1299 lung cancer cells was rescued by HDAC6 overexpression. Accordingly, the results suggested that the suppression of migration and invasion activities by honokiol was through inhibiting HDAC6‐mediated Hsp90/MMP‐9 interaction and followed by MMP‐9 degradation in lung cancer.
机译:转移是肺癌引起高死亡率的关键机制。通过蛋白水解酶,特别是基质金属蛋白酶(MMPS)的细胞外基质(ECM)的降解是促进癌细胞迁移和侵袭的关键方法。因此,靶向MMP可能是肺癌转移抑制的策略。已表明通过表观遗传调控抑制肺癌肿瘤瘤的莫冬醇。然而,通过肺癌中的象牙遗传调节通过卓越术治疗MMP介导的迁移和侵袭的调节仍然是一个谜。在本研究中,通过纯致氧体处理的非胞毒毒性浓度抑制了H1299肺癌的迁移和侵袭能力。在Honokiol处理的H1299细胞中抑制了MMP-9而不是MMP-2的蛋白水解活性。纯粹抑制的MMP-9表达是通过促进MMP-9蛋白质降解而不是抑制转录机制。此外,在檀香孵育后积累了特异性组蛋白脱乙酰酶6(HDAC6)谱系,乙酰-α-微管蛋白的表达。观察到具有超乙酰化热休克蛋白90(HSP90)的MMP-9的脱离,得到HOLOKIOL处理后MMP-9降解。同时,通过HDAC6过表达来拯救H1299肺癌细胞的MMP-9表达和侵袭能力。因此,结果表明,通过纯粹致纯化的HDAC6介导的HSP90 / MMP-9相互作用,然后在肺癌中进行MMP-9降解,抑制迁移和侵袭活性。

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