Department of Nuclear Medicine and Radiobiology, Université de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Department of Surgery, Division of Neurosurgery, Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Int J Mol Sci. 2021 Nov 10;22(22):12150. doi: 10.3390/ijms222212150.
Chemoattraction is a normal and essential process, but it can also be involved in tumorigenesis. This phenomenon plays a key role in glioblastoma (GBM). The GBM tumor cells are extremely difficult to eradicate, due to their strong capacity to migrate into the brain parenchyma. Consequently, a complete resection of the tumor is rarely a possibility, and recurrence is inevitable. To overcome this problem, we proposed to exploit this behavior by using three chemoattractants: CXCL10, CCL2 and CCL11, released by a biodegradable hydrogel (GlioGel) to produce a migration of tumor cells toward a therapeutic trap. To investigate this hypothesis, the agarose drop assay was used to test the chemoattraction capacity of these three chemokines on murine F98 and human U87MG cell lines. We then studied the potency of this approach in vivo in the well-established syngeneic F98-Fischer glioma-bearing rat model using GlioGel containing different mixtures of the chemoattractants. In vitro assays resulted in an invasive cell rate 2-fold higher when chemokines were present in the environment. In vivo experiments demonstrated the capacity of these specific chemoattractants to strongly attract neoplastic glioblastoma cells. The use of this strong locomotion ability to our end is a promising avenue in the establishment of a new therapeutic approach in the treatment of primary brain tumors.
趋化作用是一种正常且必要的过程,但它也可能参与肿瘤发生。这种现象在胶质母细胞瘤(GBM)中起着关键作用。由于 GBM 肿瘤细胞具有很强的向脑实质迁移的能力,因此极难根除。因此,完全切除肿瘤很少成为可能,复发是不可避免的。为了克服这个问题,我们提出利用三种趋化因子:CXCL10、CCL2 和 CCL11,由可生物降解的水凝胶(GlioGel)释放,以产生肿瘤细胞向治疗陷阱的迁移。为了验证这一假设,我们使用琼脂糖滴法测试了这三种趋化因子对鼠源性 F98 和人源性 U87MG 细胞系的趋化作用。然后,我们在建立良好的 F98-Fischer 同源性胶质母细胞瘤荷瘤大鼠模型中,研究了 GlioGel 中含有不同趋化因子混合物的这种方法的体内功效。体外实验结果表明,当环境中存在趋化因子时,侵袭性细胞率提高了 2 倍。体内实验证明了这些特定趋化因子强烈吸引恶性胶质母细胞瘤细胞的能力。利用这种强烈的运动能力来实现我们的目标,是在原发性脑肿瘤治疗中建立新的治疗方法的一个很有前途的途径。