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Kif11 过表达是肾透明细胞癌的一个不良预后因素。

Overexpression of kif11 is a poor prognostic factor in clear cell renal cell carcinoma.

机构信息

Chair and Department of Clinical Pathomorphology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, Poland.

Department of Tumor Pathology and Pathomorphology, Oncology Centre - Prof. Franciszek £ukaszczyk Memorial Hospital, Bydgoszcz, Poland.

出版信息

Pol J Pathol. 2022;73(2):82-87. doi: 10.5114/pjp.2022.118137.

Abstract

INTRODUCTION

Unresectable renal cell carcinoma continues to be a great challenge due to our limited understanding of its underlying pathophysiology. We explored the relationship between KIF11 protein expression and the clinical courses of clear cell renal cell carcinoma (ccRCC) using a tissue microarray.

MATERIAL AND METHODS

The tissue microarray contained specimens derived from 90 patients, cancer and matched adjacent non-cancerous tissue (2 cores per case), followed up for 7 years. Tumour samples were evaluated for KIF11 expression using the H-score, and their correlations with clinicopathological data and survival data were analysed.

RESULTS

72.7% of ccRCC tissues presented KIF11 cytoplasmic expression with a median value of 20 (interquartile range 0-200). The nuclear staining was positive in 36.36% of ccRCC tissues. Among controls, nuclear KIF11 expression was absent, but cytoplasmic expression was identified in all cases, with a median value of 230 (interquartile range 45-290). Cytoplasmic KIF11 expression in ccRCC tissues was lower than in the control tissues and was positively correlated with tumour grade and mortality (p < 0.05). KIF11 nuclear expression did not correlate with overall survival.

CONCLUSIONS

Elevated expression of KIF11 predicts poor clinical outcome in ccRCC patients. Downregulation of KIF11 may provide a new therapeutic strategy for ccRCC.

摘要

简介

由于我们对其潜在病理生理学的理解有限,因此无法切除的肾细胞癌仍然是一个巨大的挑战。我们使用组织微阵列探索了 KIF11 蛋白表达与透明细胞肾细胞癌(ccRCC)临床病程之间的关系。

材料和方法

组织微阵列包含 90 名患者的标本,癌症和匹配的相邻非癌组织(每个病例 2 个核心),随访 7 年。使用 H 评分评估肿瘤样本中的 KIF11 表达,并分析其与临床病理数据和生存数据的相关性。

结果

72.7%的 ccRCC 组织存在 KIF11 细胞质表达,中位数为 20(四分位距 0-200)。36.36%的 ccRCC 组织存在核染色阳性。在对照组中,核 KIF11 表达缺失,但所有病例均存在细胞质表达,中位数为 230(四分位距 45-290)。ccRCC 组织中的细胞质 KIF11 表达低于对照组织,与肿瘤分级和死亡率呈正相关(p < 0.05)。KIF11 核表达与总生存期无关。

结论

KIF11 表达升高预示着 ccRCC 患者的临床预后不良。下调 KIF11 可能为 ccRCC 提供新的治疗策略。

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