Tianjin Medical University, Cancer Institute and Hospital, Research Center of Basic Medical Sciences, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin 300060, China.
J Biomed Sci. 2012 May 25;19(1):53. doi: 10.1186/1423-0127-19-53.
We aimed to examine the expression level of Nucleophosmin (NPM1) protein in colon cancer tissues and to investigate the potential role of NPM1 in the regulation of cell migration and invasiveness.
Immunohistochemical assay was performed to examine the expression pattern of NPM1 in 31 groups of colonic carcinoma samples, including colon tumors, adjacent normal tissues, and matched metastatic lymph nodes from the same patients. Small interfering RNA technique and exogenous expression of wild type NPM1 methods were used to further verify the function of NPM1.
High-expression of NPM1 correlates with lymph node metastasis (P = 0.0003) and poor survival rate of human colon cancer patients (P = 0.017). SiRNA-mediated reduction of NPM1 was also shown to inhibit the migration and invasiveness of metastatic colon cancer HCT116 cell line. In addition, the exogenous expression of NPM1 in HT29 cells, a NPM1 low expression and low invasive colon cancer cell line, enhanced cell migration and invasiveness along with increased cell proliferation.
The current study uncovered the critical role of NPM1 in the regulation of colon cancer cells migration and invasion, and NPM1 may serve as a potential marker for the prognosis of colon cancer patients.
我们旨在研究核仁磷酸蛋白(NPM1)在结肠癌组织中的表达水平,并探讨 NPM1 对细胞迁移和侵袭的调控作用。
采用免疫组织化学方法检测 31 组结直肠癌样本中 NPM1 的表达模式,包括结肠癌、相邻正常组织和来自同一患者的匹配转移性淋巴结。采用小干扰 RNA 技术和外源性表达野生型 NPM1 方法进一步验证 NPM1 的功能。
NPM1 的高表达与淋巴结转移(P=0.0003)和结肠癌患者的生存率降低显著相关(P=0.017)。NPM1 的 siRNA 介导的敲低也抑制了转移性结肠癌 HCT116 细胞系的迁移和侵袭。此外,在 NPM1 低表达和侵袭性低的 HT29 细胞系中,外源性表达 NPM1 可增强细胞迁移和侵袭能力,同时促进细胞增殖。
本研究揭示了 NPM1 在调控结肠癌细胞迁移和侵袭中的关键作用,NPM1 可能成为结肠癌患者预后的潜在标志物。