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新型链霉菌来源的马努菌素 A 通过特异性蛋白 1 信号诱导人口腔鳞状细胞癌细胞发生内质网应激介导的细胞死亡。

Manumycin A from a new Streptomyces strain induces endoplasmic reticulum stress-mediated cell death through specificity protein 1 signaling in human oral squamous cell carcinoma.

机构信息

Department of Pharmacy, College of Pharmacy and Natural Medicine Research Institute, Mokpo National University, Jeonnam 534-729, Republic of Korea.

Department of Dental Pharmacology, School of Dentistry and Institute of Oral Bioscience, BK21 plus, Chonbuk National University, Jeonju 651-756, Republic of Korea.

出版信息

Int J Oncol. 2015 Nov;47(5):1954-62. doi: 10.3892/ijo.2015.3151. Epub 2015 Sep 8.

DOI:10.3892/ijo.2015.3151
PMID:26352011
Abstract

Manumycin A (Manu A) is a natural antibiotic produced by new Streptomyces strain, exhibiting antitumor and anticancer effects. However, the anticancer effects of Manu A on oral squamous cell carcinoma (OSCC) have not been reported. OSCC is an aggressive type of cancer because of its poor prognosis and low survival rate despite advanced medical treatment. We observed that Manu A reduced cell growth and Sp1 protein levels in OSCC cell lines (HN22 and HSC4) in a dose- and time-dependent manner. We also observed downregulation of Sp1 downstream target genes such as p27, p21, Mcl-1 and survivin. Moreover, nuclear staining with DAPI showed that Manu A was able to cause nuclear condensation and further fragmentation. Flow cytometry analyses using Annexin V and propiodium iodide supported Manu A-mediated apoptotic cell death of OSCC cells. Furthermore, Bcl-2 family such as mitochondrial pro‑apoptotic Bax, anti-apoptotic Bcl-xl and Bid were regulated by Manu A, triggering the mitochondrial apoptotic pathway. In conclusion, these results indicate that Manu A is a potential to treat human OSCC via cell apoptosis through the downregulation of Sp1.

摘要

马努菌素 A(Manu A)是一种新型链霉菌产生的天然抗生素,具有抗肿瘤和抗癌作用。然而,马努菌素 A 对口腔鳞状细胞癌(OSCC)的抗癌作用尚未有报道。OSCC 是一种侵袭性癌症,由于其预后不良和生存率低,尽管采用了先进的医疗方法。我们观察到马努菌素 A 以剂量和时间依赖的方式降低了 OSCC 细胞系(HN22 和 HSC4)中的细胞生长和 Sp1 蛋白水平。我们还观察到 Sp1 下游靶基因如 p27、p21、Mcl-1 和 survivin 的下调。此外,用 DAPI 进行的核染色显示马努菌素 A 能够引起核浓缩和进一步的片段化。使用 Annexin V 和碘化丙啶的流式细胞术分析支持马努菌素 A 介导的 OSCC 细胞凋亡。此外,Bcl-2 家族如线粒体促凋亡 Bax、抗凋亡 Bcl-xl 和 Bid 被马努菌素 A 调节,触发线粒体凋亡途径。总之,这些结果表明马努菌素 A 通过下调 Sp1 通过细胞凋亡来治疗人类 OSCC 具有潜力。

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