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Src激酶相关磷蛋白2的表达与非小细胞肺癌的不良预后相关。

Src kinase-associated phosphoprotein2 expression is associated with poor prognosis in non-small cell lung cancer.

作者信息

Kuranami Satoshi, Yokobori Takehiko, Mogi Akira, Altan Bolag, Yajima Toshiki, Onozato Ryoichi, Azuma Yoko, Iijima Misaki, Kosaka Takayuki, Kuwano Hiroyuki

机构信息

Department of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.

Department of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan

出版信息

Anticancer Res. 2015 Apr;35(4):2411-5.

Abstract

BACKGROUND/AIM: Non-small cell lung cancer (NSCLC) is among the leading causes of cancer-related deaths worldwide. In certain human cancer types, Src is associated with cancer progression and refractory cancer. To improve the prognoses of NSCLC patients, we evaluated Src kinase-associated phosphoprotein 2 (SKAP2), a factor associated with integrin-stimulated cytoskeletal rearrangement, as a new therapeutic target.

MATERIALS AND METHODS

We performed immunohistochemistry for SKAP2 in 99 NSCLC samples and evaluated the relationship between SKAP2 expression, clinicopathological factors and prognosis.

RESULTS

Higher SKAP2 expression was detected in cancerous tissues and was predominantly expressed in the cytoplasm. Elevated SKAP2 expression levels were associated with poor prognosis (p=0.007) and shorter survival time after recurrence (p=0.035). High SKAP2 expression was an independent prognostic factor in NSCLC patients (p=0.027).

CONCLUSION

High SKAP2 expression levels in NSCLC tissues could be a powerful biomarker of poor prognosis. Therefore, SKAP2 is a promising candidate molecular target for NSCLC treatment.

摘要

背景/目的:非小细胞肺癌(NSCLC)是全球癌症相关死亡的主要原因之一。在某些人类癌症类型中,Src与癌症进展和难治性癌症有关。为改善NSCLC患者的预后,我们评估了Src激酶相关磷蛋白2(SKAP2),一种与整合素刺激的细胞骨架重排相关的因子,作为一种新的治疗靶点。

材料与方法

我们对99例NSCLC样本进行了SKAP2免疫组织化学检测,并评估了SKAP2表达、临床病理因素与预后之间的关系。

结果

癌组织中检测到较高的SKAP2表达,且主要在细胞质中表达。SKAP2表达水平升高与预后不良(p=0.007)和复发后生存时间缩短(p=0.035)相关。高SKAP2表达是NSCLC患者的独立预后因素(p=0.027)。

结论

NSCLC组织中高SKAP2表达水平可能是预后不良的有力生物标志物。因此,SKAP2是NSCLC治疗的一个有前景的候选分子靶点。

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