Jeng Yung-Ming, Chang Cheng-Chi, Hu Fu-Chang, Chou Han-Yi E, Kao Hsin-Lien, Wang Ting-Huang, Hsu Hey-Chi
Graduate Institute of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatology. 2008 Oct;48(4):1118-27. doi: 10.1002/hep.22459.
Insulin-like growth factor II mRNA-binding protein 3 (IMP3) is an RNA-binding protein expressed in embryonic tissues and multiple cancers. To investigate the role of IMP3 in hepatocellular carcinoma (HCC), its protein expression in the surgically resected unifocal tumors of 377 HCC patients (296 men and 81 women) with ages ranging from 7 to 88 years (mean, 55.49 years) was analyzed by immunohistochemistry. IMP3 was expressed in 255 (67.6%) of 377 resected unifocal primary HCCs. IMP3 protein was predominantly expressed in tumor border and invasive front, and it was more abundant in the satellite nodules and tumor thrombi than in the main tumors. The expression correlated with high alpha-fetoprotein (>200 ng/mL, P < 1 x 10(-7)), larger tumor size (>5 cm, P = 0.006), high tumor grade (P < 1 x 10(-7)), and high tumor stage with vascular invasion and various degrees of intrahepatic metastasis (P < 1 x 10(-7)). IMP3 expression predicted early tumor recurrence (P < 1 x 10(-7)) and was a strong indicator of poor prognosis (P < 0.0001). Depletion of IMP3 with RNA interference in HCC cell line HA22T caused a decrease in cell motility, invasion, and transendothelial migration. Microarray analysis revealed that IMP3 depletion was associated with downregulation of multiple genes involved in tumor invasion.
Our results indicate that IMP3 plays an important role in tumor invasion and metastasis and is a strong prognostic factor for patients with HCC.
胰岛素样生长因子II mRNA结合蛋白3(IMP3)是一种在胚胎组织和多种癌症中表达的RNA结合蛋白。为了研究IMP3在肝细胞癌(HCC)中的作用,通过免疫组织化学分析了377例年龄在7至88岁(平均55.49岁)的HCC患者(296例男性和81例女性)手术切除的单发病灶肿瘤中IMP3的蛋白表达情况。IMP3在377例切除的单发性原发性HCC中的255例(67.6%)中表达。IMP3蛋白主要在肿瘤边界和浸润前沿表达,在卫星结节和肿瘤血栓中比在主要肿瘤中更丰富。该表达与高甲胎蛋白(>200 ng/mL,P < 1×10⁻⁷)、较大肿瘤大小(>5 cm,P = 0.006)、高肿瘤分级(P < 1×10⁻⁷)以及伴有血管侵犯和不同程度肝内转移的高肿瘤分期(P < 1×10⁻⁷)相关。IMP3表达可预测肿瘤早期复发(P < 1×10⁻⁷),并且是预后不良的有力指标(P < 0.0001)。在HCC细胞系HA22T中用RNA干扰耗尽IMP3会导致细胞运动性、侵袭和跨内皮迁移减少。微阵列分析显示,IMP3耗尽与参与肿瘤侵袭的多个基因的下调有关。
我们的结果表明,IMP3在肿瘤侵袭和转移中起重要作用,并且是HCC患者的有力预后因素。