Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
PLoS One. 2013;8(2):e55894. doi: 10.1371/journal.pone.0055894. Epub 2013 Feb 6.
Period1 (PER1) is an important core clock gene, which regulates normal cell proliferations and physiological rhythms of human beings. Recent studies have showed aberrant expressions and altered rhythms of PER1 were highly correlated to the carcinogenesis and development of malignant tumors. However, there is no study on the correlation of aberrant expressions and altered rhythms of PER1 with the growth, proliferation and metastasis of buccal squamous cell carcinoma (BSCC). In this study, PER1 and MMP-2 expression in the cancerous and adjacent noncancerous tissues of 38 patients with BSCC and its correlations with patients' clinical pathologic characteristics were investigated. A mouse model of BSCC was also established and mice were sacrificed at 4 different time points in a period of 24 hours. Xenografted tumor weight, proliferation index (PI), and mitotic index (MI) of tumors in the 4 time groups were detected. Results showed that PER1 expression was significantly down-regulated in cancerous tissues of patients with BSCC (P<0.05). PER1 expression was significantly down-regulated in patients of T3∼T4 staging and those with lymph node metastasis compared to that of T1∼T2 staging and those without lymph node metastasis (P<0.05), respectively. PER1 mRNA expression, MI and tumor weight had significant differences among the 4 time groups, which PI all confirmed to circadian rhythms. MI, PI, MMP-2 mRNA and tumor weight had negative correlation with PER1 mRNA expression. Peak value of PER1 mRNA expression and trough values of MI, PI and tumor weight all appeared in middle activity phase, whereas trough value of PER1 mRNA expression and peak values of MI, PI and tumor weight all occurred in middle rest phase. Our study suggested that aberrant expression of PER1 had significant correlation with the growth, proliferation and metastasis of BSCC and it might act as an anti-oncogene.
PER1 是一个重要的核心时钟基因,调节着人类正常的细胞增殖和生理节律。最近的研究表明,PER1 的异常表达和节律改变与恶性肿瘤的发生发展高度相关。然而,目前还没有研究表明 PER1 的异常表达和节律改变与颊鳞状细胞癌(BSCC)的生长、增殖和转移有关。本研究检测了 38 例 BSCC 患者癌组织和癌旁非癌组织中 PER1 和 MMP-2 的表达,并探讨了其与患者临床病理特征的关系。同时还建立了 BSCC 小鼠模型,在 24 小时的 4 个不同时间点处死小鼠,检测 4 个时间点的移植瘤重量、增殖指数(PI)和有丝分裂指数(MI)。结果表明,BSCC 患者癌组织中 PER1 表达明显下调(P<0.05)。T3∼T4 期和有淋巴结转移的患者 PER1 表达明显低于 T1∼T2 期和无淋巴结转移的患者(P<0.05)。PER1 mRNA 表达、MI 和肿瘤重量在 4 个时间组之间存在显著差异,PI 均证实存在昼夜节律。MI、PI、MMP-2 mRNA 和肿瘤重量与 PER1 mRNA 表达呈负相关。PER1 mRNA 表达的峰值和 MI、PI 和肿瘤重量的低谷值均出现在中活动期,而 PER1 mRNA 表达的低谷值和 MI、PI 和肿瘤重量的峰值均出现在中休息期。本研究表明,PER1 的异常表达与 BSCC 的生长、增殖和转移密切相关,可能作为一种抑癌基因发挥作用。