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促红细胞生成素及其受体在人肾细胞癌中的表达

Expression of erythropoietin and its receptor in human renal cell carcinoma.

作者信息

Papworth Karin, Bergh Anders, Grankvist Kjell, Ljungberg Börje, Rasmuson Torgny

机构信息

Department of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden.

出版信息

Tumour Biol. 2009;30(2):86-92. doi: 10.1159/000216844. Epub 2009 May 4.

Abstract

OBJECTIVE

To investigate the prognostic impact of erythropoietin (EPO) and EPO-receptor (EPO-R) expression in tumour as well as serum EPO in patients with renal cell carcinoma (RCC).

METHODS

Using immunohistochemistry, EPO and EPO-R were assessed in tissue microarrays from 195 RCCs. RCC type, TNM stage, nuclear grade, survival, EPO and haemoglobin (Hb) levels in blood were registered.

RESULTS

Strong expression of EPO and EPO-R in tumour tissue was found in 83 and 56%, respectively. EPO and EPO-R expression differed between RCC types. Serum EPO and blood Hb did not correlate to the expression of EPO or EPO-R. A positive correlation was found between the expression of EPO and EPO-R (p = 0.028). Survival was not related to tumour EPO, whereas strong EPO-R expression indicated a non-significantly worse prognosis. Serum EPO correlated positively to TNM stage and nuclear grade and negatively to survival. A multivariate analysis showed that TNM stage and nuclear grade were independent prognostic factors. Tumour EPO and EPO-R expression as well as serum EPO added no independent prognostic information.

CONCLUSION

No correlation between EPO or EPO-R in tumour tissue and serum EPO or blood Hb was found. Neither EPO, EPO-R in tumour tissue nor serum EPO are independent prognostic factors.

摘要

目的

研究促红细胞生成素(EPO)和EPO受体(EPO-R)在肿瘤中的表达以及血清EPO对肾细胞癌(RCC)患者预后的影响。

方法

采用免疫组织化学方法,对195例RCC组织芯片中的EPO和EPO-R进行评估。记录RCC类型、TNM分期、核分级、生存率、血液中的EPO和血红蛋白(Hb)水平。

结果

肿瘤组织中EPO和EPO-R的强表达分别见于83%和56%的病例。EPO和EPO-R的表达在不同RCC类型之间存在差异。血清EPO和血液Hb与EPO或EPO-R的表达无关。EPO和EPO-R的表达之间存在正相关(p = 0.028)。生存率与肿瘤EPO无关,而EPO-R的强表达提示预后稍差但无统计学意义。血清EPO与TNM分期和核分级呈正相关,与生存率呈负相关。多因素分析显示TNM分期和核分级是独立的预后因素。肿瘤EPO和EPO-R的表达以及血清EPO均未增加独立的预后信息。

结论

未发现肿瘤组织中的EPO或EPO-R与血清EPO或血液Hb之间存在相关性。肿瘤组织中的EPO、EPO-R以及血清EPO均不是独立的预后因素。

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