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首页> 外文期刊>Cancer biology & therapy >Mycobacterium indicus pranii (Mw) inhibits invasion by reducing matrix metalloproteinase (MMP-9) via AKT/ERK-1/2 and PKCα signaling: A potential candidate in melanoma cancer therapy
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Mycobacterium indicus pranii (Mw) inhibits invasion by reducing matrix metalloproteinase (MMP-9) via AKT/ERK-1/2 and PKCα signaling: A potential candidate in melanoma cancer therapy

机译:通过AKT / ERK-1/2和PKCα信号传导还原基质金属蛋白酶(MMP-9)和PKCα信号传导来抑制侵袭血糖杆菌(MW):黑素瘤癌症治疗中的潜在候选者

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摘要

Invasion and metastasis via induction of matrix metalloproteinases are the main causes of death in melanoma cancer. In this study, we investigated the inhibitory effects of heat killed saprophytic bacterium Mycobacterium indicus pranii (Mw) on B16F10 melanoma cell invasion. Mw reported to be an immunomodulator has antitumor activity however, its effect on cancer cell invasion has not been studied. Highly invasive B16F10 melanoma was found sensitive to Mw which downregulated MMP-9 expression. Mw treatment inhibited nuclear factor-κB (NF-κB) and activator protein-1 (AP-1) transcriptional activity and respective DNA binding to MMP-9 promoter. Moreover, Mw also overcame the promoting effects of PMA on B16F10 cell invasion. Mw decreased PMA-induced transcriptional activation of NF-κB and AP-1 by inhibiting phosphorylation of AKT and ERK-1/2. Furthermore, Mw strongly suppressed PMA-induced membrane localization of protein kinase C α (PKCα) since PKCα inhibition caused a marked decrease in PMA-induced MMP-9 secretion as well as AKT/ERK-1/2 activation. These results suggest that Mw may be a promising anti-invasive agent as it blocks tumor growth and inhibits B16F10 cell invasion by reducing MMP-9 activation through inhibition of PKCα/ AKT/ ERK-1/2 phosphorylation and NF-κB/AP-1 activation.
机译:通过诱导基质金属蛋白酶诱导侵袭和转移是黑素瘤癌症中死亡的主要原因。在这项研究中,我们研究了热杀死的脂肪菌细菌的抑制作用PRANII(MW)对B16F10黑色素瘤细胞侵袭。据报道,MW是免疫调节器具有抗肿瘤活性然而,其对癌细胞侵袭的影响尚未研究。高度侵袭性B16F10黑色素瘤对MW的敏感性,其下调MMP-9表达。 MW治疗抑制核因子-κB(NF-κB)和活化剂蛋白-1(AP-1)转录活性以及与MMP-9启动子的各自的DNA结合。此外,MW还克服了PMA对B16F10细胞侵袭的促进效果。通过抑制AKT和ERK-1/2的磷酸化,MW降低了PMA诱导的NF-κB和AP-1的转录激活。此外,MW强制抑制蛋白激酶Cα(PKCα)的PMA诱导的膜定位,因为PKCα抑制引起PMA诱导的MMP-9分泌和AKT / ERK-1/2活化的显着降低。这些结果表明,MW可能是一种有前途的抗侵入剂,因为它阻断肿瘤生长并通过通过抑制PKCα/ AKT / ERK-1/2磷酸化和NF-κB/ AP-1来抑制MMP-9活化来抑制B16F10细胞侵袭激活。

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