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使用SU6656、PP2和达沙替尼靶向头颈部肿瘤细胞中的Src家族激酶

Src family kinase targeting in head and neck tumor cells using SU6656, PP2 and dasatinib.

作者信息

Vu Anh Thu, Akingunsade Lara, Hoffer Konstantin, Petersen Cordula, Betz Christian Stephan, Rothkamm Kai, Rieckmann Thorsten, Bussmann Lara, Kriegs Malte

机构信息

Department of Radiobiology & Radiation Oncology, Hubertus Wald Tumorzentrum - University Cancer Center Hamburg (UCCH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

UCCH Kinomics Core Facility, Hubertus Wald Tumorzentrum - University Cancer Center Hamburg (UCCH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Head Neck. 2023 Jan;45(1):147-155. doi: 10.1002/hed.27216. Epub 2022 Oct 25.

Abstract

BACKGROUND

We have recently shown a frequent upregulation of Src-family kinases (SFK) in head and neck squamous cell carcinoma (HNSCC). Here we tested, if SFK targeting is effective especially in HNSCC cells with upregulated SFK signaling.

METHODS

The impact of SFK inhibitors SU6656, PP2 and dasatinib on three HNSCC cell lines with different SFK activity levels was analyzed using proliferation and colony formation assays, Western blot and functional kinomics.

RESULTS

Proliferation was blocked by all inhibitors in a micro-molar range. With respect to cell kill, dasatinib was most effective, while SU6656 showed moderate and PP2 minor effects. Cellular signaling was affected differently, with PP2 having no effect on SFK signaling while dasatinib probably has non-SFK specific effects. Only SU6656 showed clear SFK specific effects on signaling.

CONCLUSION

The results demonstrate potential benefit of SFK inhibition in HNSCC but they also highlight challenges due to non-specificities of the different drugs.

摘要

背景

我们最近发现头颈部鳞状细胞癌(HNSCC)中Src家族激酶(SFK)频繁上调。在此,我们测试了靶向SFK是否对SFK信号上调的HNSCC细胞特别有效。

方法

使用增殖和集落形成试验、蛋白质印迹法和功能激酶组学分析了SFK抑制剂SU6656、PP2和达沙替尼对三种具有不同SFK活性水平的HNSCC细胞系的影响。

结果

所有抑制剂在微摩尔范围内均能阻断增殖。就细胞杀伤而言,达沙替尼最有效,而SU6656显示出中等效果,PP2效果较小。细胞信号传导受到不同影响,PP2对SFK信号传导无影响,而达沙替尼可能具有非SFK特异性作用。只有SU6656对信号传导显示出明显的SFK特异性作用。

结论

结果证明了抑制SFK在HNSCC中的潜在益处,但也突出了不同药物非特异性带来的挑战。

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