FGFR抑制作为一种新的治疗策略使胶质母细胞瘤干细胞对肿瘤治疗场敏感。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY
Pauline Deshors, Ziad Kheil, Laetitia Ligat, Valerie Gouazé-Andersson, Elizabeth Cohen-Jonathan Moyal
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引用次数: 0

摘要

胶质母细胞瘤(GBM)是侵袭性肿瘤,尽管标准治疗相关手术,化疗和放疗,但仍会系统性复发。最近,GBM治疗现在包括另一种治疗方式选择,肿瘤治疗场(TTFields)在标准治疗后与替莫唑胺(TMZ)联合给予。然而,即使与TTFields结合,由于治疗耐药性,GBM仍然是一种致命疾病。耐药的原因之一是癌症干细胞(GSC)的存在,已知其具有化疗和放射抗性,并负责肿瘤再生。因此,研究GSC对TTFields的抗性机制是一个重要的问题。成纤维细胞生长因子受体(FGFR)在癌症发展的许多重要过程中发挥重要作用,FGFR信号传导失调已在许多癌症类型中观察到,包括GBM。我们之前已经表明,酪氨酸激酶受体成纤维细胞生长因子受体1 (FGFR1)控制GBM侵袭性和GSC放射抗性,并且其抑制作用通过增加有丝分裂细胞死亡和微环境调节导致放射增敏。由于TTFields的主要作用机制之一是有丝分裂干扰,并且由于TTFields在体外与辐照(IR)协同作用,我们假设靶向FGFR可以使GSC对TTFields敏感。这里我们表明,像IR一样,TTFields显著降低GSC的生长。用pemigatinib (Pem)(一种FGFR1-3抑制剂)治疗GSC可改变FGFR信号通路。我们证明Pem通过协同降低GSC的存活和克隆生成能力使其对TTFields敏感。最后,将Pem与IR和TTFields联合处理可以通过诱导某些GSC进一步减少IR诱导的DNA损伤的修复而使GSC敏化。总之,这些结果突出了TTFields在一线标准GBM治疗中抑制FGFR以改善患者预后的潜在益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FGFR inhibition as a new therapeutic strategy to sensitize glioblastoma stem cells to tumor treating fields.

Glioblastomas (GBM) are aggressive tumors, which systematically relapse despite standard treatment associating surgery, chemotherapy and radiation therapy. More recently, GBM therapy now includes another therapeutic modality option, Tumor Treating Fields (TTFields) given in combination with Temozolomide (TMZ) following standard treatment. However even with the adjunction of TTFields, GBM remains a lethal disease due to treatment resistance. One of the causes of resistance is the presence of cancer stem cells (GSC) known to be chemo and radioresistant and responsible for tumor regrowth. Studying mechanisms of resistance of GSC to TTFields is thus a major issue to address. Fibroblast Growth Factor Receptors (FGFR) play a major role in numerous processes essential for cancer development, and dysregulation of FGFR signaling has been observed in many cancer types, including GBM. We have previously shown that tyrosine kinase receptor Fibroblast Growth Factor Receptor 1 (FGFR1) controls GBM aggressiveness and GSC radioresistance and that its inhibition leads to radiosensitization through increasing mitotic cell death and microenvironment modulation. Because one of the main mechanisms of action of TTFields is mitotic disturbance and because TTFields act synergistically in vitro with irradiation (IR), we hypothesize that targeting FGFR could sensitize GSC to TTFields. Here we show that, like IR, TTFields significantly decrease GSC growth. Treatment of GSC with pemigatinib (Pem), a FGFR1-3 inhibitor, alters FGFR signalling pathway. We demonstrate that Pem, sensitizes GSC to TTFields by synergistically decreasing their survival and clonogenic ability. Finally, the adjunction of Pem to treatment combining IR and TTFields could sensitize GSC by inducing, in some GSC, a further decrease in the repair of IR-induced DNA damages. Altogether, these results highlight the potential benefits of inhibiting FGFR with the concomitant application of TTFields in the first-line standard GBM treatment to improve patient prognosis.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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