研究动态
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5-氨基乙酰丙酸介导的光动力疗法与激酶抑制剂拉帕替尼联合可增强胶质母细胞瘤细胞死亡。

5-Aminolevulinic acid-mediated photodynamic therapy in combination with kinase inhibitor lapatinib enhances glioblastoma cell death.

发表日期:2024 Aug 27
作者: Sharayu Chandratre, Daniel Merenich, Kenneth Myers, Bin Chen
来源: Cell Death & Disease

摘要:

5-氨基乙酰丙酸 (ALA) 是一种术中显像剂,被批准用于原卟啉 IX (PpIX) 荧光引导的胶质母细胞瘤 (GBM) 切除术。目前正在进行 GBM 手术完成后光动力疗法 (PDT) 的临床评估。我们之前展示了拉帕替尼,一种表皮生长因子受体 1 的临床激酶抑制剂
5-Aminolevulinic acid (ALA) is an intraoperative imaging agent approved for protoporphyrin IX (PpIX) fluorescence-guided resection of glioblastoma (GBM). It is currently under clinical evaluation for photodynamic therapy (PDT) after the completion of GBM surgery. We previously showed that lapatinib, a clinical kinase inhibitor of epidermal growth factor receptor 1 & 2 (EGFR and HER2), enhanced PpIX fluorescence in a panel of GBM cell lines by blocking ABCG2 (ATP-binding cassette super-family G member 2)-mediated PpIX efflux, which suggests its potential for improving ALA for GBM surgery and PDT. Here we show that lapatinib enhanced PDT-induced cytotoxicity by promoting GBM cell death with the induction of apoptosis followed by necrosis. While the induction of tumor cell apoptosis was massive and rapid in the H4 cell line with no detectable Bcl-2 and a low level of Bcl-xL, it was delayed and much less in extent in A172, U-87 and U-118 cell lines with higher levels of pro-survival Bcl-2 family proteins. Lapatinib treatment alone neither reduced GBM cell viability nor had any significant effect on EGFR downstream signaling. Its enhancement of ALA-PDT was largely due to the increase of intracellular PpIX particularly in the mitochondria, resulting in the activation of mitochondria-mediated apoptosis in H4 cells. Our present study demonstrates that lapatinib inhibits ABCG2-mediated PpIX efflux and sensitizes GBM cells to ALA-PDT by inducing tumor cell death.© 2024. The Author(s).