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Nup88表达在结直肠癌患者中的临床病理意义

Clinicopathological significance of Nup88 expression in patients with colorectal cancer.

作者信息

Emterling Anna, Skoglund Johanna, Arbman Gunnar, Schneider Jose, Evertsson Sofia, Carstensen John, Zhang Hong, Sun Xiao-Feng

机构信息

Department of Oncology, Institute of Biomedicine and Surgery, Linköping University, Linköping, Sweden.

出版信息

Oncology. 2003;64(4):361-9. doi: 10.1159/000070294.

Abstract

OBJECTIVE

The nucleoporin Nup88 is overexpressed in a series of human malignancies, however, its clinicopathological significance has not been studied. Our aims were to analyze Nup88 expression in normal mucosa, primary tumors and metastases from colorectal cancer patients and further to identify relationships of Nup88 expression with clinicopathological and other factors.

MATERIALS AND METHODS

Using immunohistochemistry, we investigated Nup88 expression in 198 primary colorectal tumors, 96 normal mucosa samples and 35 lymph node metastases.

RESULTS

The results showed that the intensity of Nup88 expression increased from the normal mucosa to the primary tumors (p < 0.0001) and tended to increase from the primary tumors to the metastases (p = 0.15). Both primary tumors and metastases presented stronger expression in the invasive margin and vascular-invaded areas. Nup88 expression was positively related to distal tumor location (p = 0.01), infiltrative growth pattern (p = 0.04) and higher proliferative activity (p = 0.04) and reversely to the grade of differentiation (p = 0.02) and apoptosis (p = 0.049). Strong expression of Nup88 predicted a worse outcome in the patients with distal tumors during the follow-up period of up to 3 years (p = 0.02).

CONCLUSIONS

It seems that overexpression of Nup88 was involved in the tumorigenesis and aggressiveness of colorectal cancers, and Nup88 may be used as a prognostic factor in patients with distal tumors.

摘要

目的

核孔蛋白Nup88在一系列人类恶性肿瘤中过表达,然而,其临床病理意义尚未得到研究。我们的目的是分析Nup88在结直肠癌患者的正常黏膜、原发性肿瘤和转移灶中的表达,并进一步确定Nup88表达与临床病理及其他因素之间的关系。

材料与方法

我们采用免疫组织化学方法,研究了198例原发性结直肠癌肿瘤、96例正常黏膜样本和35例淋巴结转移灶中Nup88的表达情况。

结果

结果显示,Nup88表达强度从正常黏膜到原发性肿瘤逐渐增加(p < 0.0001),从原发性肿瘤到转移灶有增加趋势(p = 0.15)。原发性肿瘤和转移灶在浸润边缘和血管侵犯区域均呈现更强的表达。Nup88表达与肿瘤远端位置(p = 0.01)、浸润性生长模式(p = 0.04)和较高的增殖活性(p = 0.04)呈正相关,与分化程度(p = 0.02)和凋亡(p = 0.049)呈负相关。在长达3年的随访期内,Nup88的强表达预示着远端肿瘤患者预后较差(p = 0.02)。

结论

似乎Nup88的过表达参与了结直肠癌的肿瘤发生和侵袭性,并且Nup88可作为远端肿瘤患者的预后因素。

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