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索凡替尼联合光动力疗法在肿瘤模型中诱导铁死亡以抑制胆管癌。

Surufatinib combined with photodynamic therapy induces ferroptosis to inhibit cholangiocarcinoma and in tumor models.

作者信息

Huang Yun-Peng, Wang Yong-Xiang, Zhou Hui, Liu Zhong-Tao, Zhang Zi-Jian, Xiong Li, Zou Heng, Wen Yu

机构信息

Department of General Surgery, The Second Xiangya Hospital of Central South University, Changsha, China.

出版信息

Front Pharmacol. 2024 Apr 5;15:1288255. doi: 10.3389/fphar.2024.1288255. eCollection 2024.

Abstract

The curative effect of single therapy for advanced cholangiocarcinoma (CCA) is poor, thus investigating combined treatment strategies holds promise for improving prognosis. Surufatinib (SUR) is a novel multikinase inhibitor that has been confirmed to prolong survival of patients with advanced CCA. Photodynamic therapy (PDT) can also ablate advanced CCA and relieve biliary obstruction. In this study, we explored the anti-CCA effect of SUR combined with PDT, and explored the underlying mechanism. We found that SUR could effectively inhibit the abilities of proliferation, migration and metastasis in CCA cells (HUCCT-1, RBE). The ability of SUR to inhibit CCA was also confirmed by the HUCCT-1 cell xenograft model in Balb/c nude mice and CCA patient-derived organoids. SUR combined with PDT can significantly enhance the inhibitory effect on CCA, and can be alleviated by two ferroptosis inhibitors (Ferrostatin-1, Deferoxamine). By detecting the level of reactive oxygen species, lipid peroxides, malondialdehyde and glutathione, we further confirmed that SUR combined with PDT can inhibit CCA cells by inducing ferroptosis. Glutathione peroxidase 4 (GPX4) belongs to the glutathione peroxidase family and is mainly responsible for the metabolism of intracellular hydrogen peroxide. GPX4 inhibits ferroptosis by reducing cytotoxic lipid peroxides (L-OOH) to the corresponding alcohols (L-OH). Acyl-CoA synthetase long-chain family member 4 (ACSL4) is a member of the long-chain fatty acid coenzyme a synthetase family and is mainly involved in the biosynthesis and catabolism of fatty acids. ACSL4 induces ferroptosis by promoting the accumulation of lipid peroxides. Both SUR and PDT can induce ferroptosis by promoting ACSL4 and inhibiting GPX4. The regulation effect is found to be more significant in combined treatment group. In conclusion, SUR combined with PDT exerted an anti-CCA effect by inducing ferroptosis. Combination therapy provides a new idea for the clinical treatment of CCA.

摘要

晚期胆管癌(CCA)的单一疗法疗效不佳,因此研究联合治疗策略有望改善预后。索凡替尼(SUR)是一种新型多激酶抑制剂,已被证实可延长晚期CCA患者的生存期。光动力疗法(PDT)也可消融晚期CCA并缓解胆道梗阻。在本研究中,我们探讨了SUR联合PDT的抗CCA作用,并探究其潜在机制。我们发现SUR可有效抑制CCA细胞(HUCCT-1、RBE)的增殖、迁移和转移能力。Balb/c裸鼠的HUCCT-1细胞异种移植模型和CCA患者来源的类器官也证实了SUR抑制CCA的能力。SUR联合PDT可显著增强对CCA的抑制作用,且两种铁死亡抑制剂(铁抑素-1、去铁胺)可减轻这种作用。通过检测活性氧、脂质过氧化物、丙二醛和谷胱甘肽水平,我们进一步证实SUR联合PDT可通过诱导铁死亡抑制CCA细胞。谷胱甘肽过氧化物酶4(GPX4)属于谷胱甘肽过氧化物酶家族,主要负责细胞内过氧化氢的代谢。GPX4通过将细胞毒性脂质过氧化物(L-OOH)还原为相应的醇(L-OH)来抑制铁死亡。酰基辅酶A合成酶长链家族成员4(ACSL4)是长链脂肪酸辅酶A合成酶家族的成员,主要参与脂肪酸的生物合成和分解代谢。ACSL4通过促进脂质过氧化物的积累诱导铁死亡。SUR和PDT均可通过促进ACSL4和抑制GPX4诱导铁死亡。联合治疗组的调节作用更为显著。综上所述,SUR联合PDT通过诱导铁死亡发挥抗CCA作用。联合治疗为CCA的临床治疗提供了新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/11027741/0cd2a14302a9/fphar-15-1288255-g001.jpg

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