Kamarajan Pachiyappan, Hayami Takayuki, Matte Bibiana, Liu Yang, Danciu Theodora, Ramamoorthy Ayyalusamy, Worden Francis, Kapila Sunil, Kapila Yvonne
Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Department of Orthodontics and Pediatric Dentistry, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS One. 2015 Jul 1;10(7):e0131008. doi: 10.1371/journal.pone.0131008. eCollection 2015.
The use of small antimicrobial peptides or bacteriocins, like nisin, to treat cancer is a new approach that holds great promise. Nisin exemplifies this new approach because it has been used safely in humans for many years as a food preservative, and recent laboratory studies support its anti-tumor potential in head and neck cancer. Previously, we showed that nisin (2.5%, low content) has antitumor potential in head and neck squamous cell carcinoma (HNSCC) in vitro and in vivo. The current studies explored a naturally occurring variant of nisin (nisin ZP; 95%, high content) for its antitumor effects in vitro and in vivo. Nisin ZP induced the greatest level of apoptosis in HNSCC cells compared to low content nisin. HNSCC cells treated with increasing concentrations of nisin ZP exhibited increasing levels of apoptosis and decreasing levels of cell proliferation, clonogenic capacity, and sphere formation. Nisin ZP induced apoptosis through a calpain-dependent pathway in HNSCC cells but not in human oral keratinocytes. Nisin ZP also induced apoptosis dose-dependently in human umbilical vein endothelial cells (HUVEC) with concomitant decreases in vascular sprout formation in vitro and reduced intratumoral microvessel density in vivo. Nisin ZP reduced tumorigenesis in vivo and long-term treatment with nisin ZP extended survival. In addition, nisin treated mice exhibited normal organ histology with no evidence of inflammation, fibrosis or necrosis. In summary, nisin ZP exhibits greater antitumor effects than low content nisin, and thus has the potential to serve as a novel therapeutic for HNSCC.
使用小抗菌肽或细菌素(如乳链菌肽)来治疗癌症是一种极具前景的新方法。乳链菌肽就是这种新方法的典型代表,因为它作为食品防腐剂已在人类中安全使用多年,并且最近的实验室研究支持其对头颈部癌症的抗肿瘤潜力。此前,我们表明乳链菌肽(2.5%,低含量)在体外和体内对头颈部鳞状细胞癌(HNSCC)具有抗肿瘤潜力。当前的研究探索了乳链菌肽的一种天然变体(乳链菌肽ZP;95%,高含量)在体外和体内的抗肿瘤作用。与低含量乳链菌肽相比,乳链菌肽ZP在HNSCC细胞中诱导的凋亡水平最高。用浓度不断增加的乳链菌肽ZP处理的HNSCC细胞,其凋亡水平不断升高,而细胞增殖、克隆形成能力和球体形成水平则不断降低。乳链菌肽ZP通过钙蛋白酶依赖性途径在HNSCC细胞中诱导凋亡,但在人口腔角质形成细胞中则不然。乳链菌肽ZP还在人脐静脉内皮细胞(HUVEC)中剂量依赖性地诱导凋亡,同时在体外血管芽形成减少,在体内肿瘤内微血管密度降低。乳链菌肽ZP在体内降低了肿瘤发生,并且用乳链菌肽ZP长期治疗可延长生存期。此外,用乳链菌肽处理的小鼠器官组织学正常,没有炎症、纤维化或坏死的迹象。总之,乳链菌肽ZP比低含量乳链菌肽表现出更强的抗肿瘤作用,因此有潜力作为HNSCC的一种新型治疗方法。