Institute for Molecular Oncology, Radio-Biology and Experimental Radiotherapy, Universitätsklinikum Marien Hospital Herne, Ruhr-Universität Bochum, Herne, Germany.
Universitätsklinikum Marien Hospital, Hölkeskampring 40, 44265, Herne, Germany.
Radiat Oncol. 2019 Feb 4;14(1):25. doi: 10.1186/s13014-019-1230-3.
Radiotherapy is administered in more than 60% of all solid tumors. Most patients are cured but a significant number develops local recurrences or distant metastases. The question arises if irradiation might influence the metastatic process. In the present study we examined whether the adhesion of glioblastoma or breast cancer cells to endothelial cells, an important step in metastasis, is affected by photon irradiation.
U-87 MG, U-373 MG and MDA-MB-231 cancer cells as well as primary human endothelial cells were irradiated with 0, 2, 4, or 8 Gy photons at a dose rate of 5 Gy/min. The adhesion of cancer cells to endothelial cells was tested either with the Vybrant based assay via fluorescent labelling or with an ibidi pump system able to mimic the physiological blood flow in vitro. In addition, the impact of FAK (focal adhesion kinase) inhibitor PF-573, 228 on the adhesion of non-irradiated and irradiated tumor cells was analyzed. Adhesion related and regulated proteins were analyzed by Western blotting.
The cellular adhesion was increased after irradiation regardless of which cell type was irradiated. The FAK-inhibitor was able to reduce the adhesion of non-irradiated cells but also the irradiation-induced increase in adhesion of tumor cells to endothelium. Adhesion related proteins were enhanced after irradiation with 4 Gy or 8 Gy in both cells types. The increased adhesion after irradiation is accompanied by the phosphorylation of src (Y416), FAK (Y397) and increased expression of paxillin.
Irradiation with photons in therapeutic doses is able to enhance the interaction between tumor cells and endothelial cells and by that might influence important steps of the metastatic process.
放疗应用于超过 60%的实体肿瘤。大多数患者得以治愈,但仍有相当一部分患者出现局部复发或远处转移。由此产生疑问,放疗是否会影响转移过程。本研究旨在探讨光子照射是否会影响胶质母细胞瘤或乳腺癌细胞黏附至内皮细胞这一转移过程中的重要步骤。
用 0、2、4 或 8Gy 光子剂量率 5Gy/min 对 U-87MG、U-373MG 和 MDA-MB-231 癌细胞以及原代人内皮细胞进行照射。采用基于 Vybrant 的荧光标记检测法或能够模拟体外生理血流的 ibidi 泵系统检测癌细胞与内皮细胞的黏附。此外,还分析了 FAK(粘着斑激酶)抑制剂 PF-573,228 对非照射和照射肿瘤细胞黏附的影响。通过 Western blot 分析黏附相关和调节蛋白。
无论哪种细胞类型被照射,细胞黏附性在照射后均增加。FAK 抑制剂能够降低非照射细胞的黏附性,同时也降低了照射后肿瘤细胞与内皮细胞的黏附性增加。两种细胞类型在接受 4Gy 或 8Gy 照射后,黏附相关蛋白均增强。照射后黏附增加伴随着 src(Y416)、FAK(Y397)的磷酸化以及桩蛋白表达增加。
在治疗剂量下,光子照射能够增强肿瘤细胞与内皮细胞之间的相互作用,从而影响转移过程中的重要步骤。