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靶向抑制素抑制黑色素瘤生长并克服靶向治疗耐药性。

Targeting Prohibitins to Inhibit Melanoma Growth and Overcome Resistance to Targeted Therapies.

机构信息

Laboratory of Clinical and Experimental Oncology (LOCE), Institut Jules Bordet, Université Libre de Bruxelles, 1000 Brussels, Belgium.

Department of Medical Oncology, Institut Jules Bordet, Université Libre de Bruxelles, 1070 Brussels, Belgium.

出版信息

Cells. 2023 Jul 14;12(14):1855. doi: 10.3390/cells12141855.

Abstract

Despite important advances in the treatment of metastatic melanoma with the development of MAPK-targeted agents and immune checkpoint inhibitors, the majority of patients either do not respond to therapies or develop acquired resistance. Furthermore, there is no effective targeted therapy currently available for BRAF wild-type melanomas (approximately 50% of cutaneous melanoma). Thus, there is a compelling need for new efficient targeted therapies. Prohibitins (PHBs) are overexpressed in several types of cancers and implicated in the regulation of signaling networks that promote cell invasion and resistance to cell apoptosis. Herein, we show that PHBs are highly expressed in melanoma and are associated with not only poor survival but also with resistance to BRAFi/MEKi. We designed and identified novel specific PHB inhibitors that can inhibit melanoma cell growth in 3D spheroid models and a large panel of representative cell lines with different molecular subtypes, including those with intrinsic and acquired resistance to MAPKi, by significantly moderating both MAPK (CRAF-ERK axis) and PI3K/AKT pathways, and inducing apoptosis through the mitochondrial pathway and up-regulation of p53. In addition, autophagy inhibition enhances the antitumor efficacy of these PHB ligands. More important, these ligands can act in synergy with MAPKi to more efficiently inhibit cell growth and overcome drug resistance in both BRAF wild-type and mutant melanoma. In conclusion, targeting PHBs represents a very promising therapeutic strategy in melanoma, regardless of mutational status.

摘要

尽管 MAPK 靶向药物和免疫检查点抑制剂的发展在转移性黑色素瘤的治疗方面取得了重要进展,但大多数患者要么对治疗无反应,要么产生获得性耐药。此外,目前对于 BRAF 野生型黑色素瘤(约占皮肤黑色素瘤的 50%)尚无有效的靶向治疗方法。因此,迫切需要新的高效靶向治疗方法。抑素(PHBs)在多种类型的癌症中过度表达,并与促进细胞侵袭和抵抗细胞凋亡的信号网络的调节有关。在此,我们表明 PHBs 在黑色素瘤中高度表达,不仅与不良预后相关,而且与 BRAFi/MEKi 耐药相关。我们设计并鉴定了新型特异性 PHB 抑制剂,这些抑制剂可以通过显著调节 MAPK(CRAF-ERK 轴)和 PI3K/AKT 通路,以及通过线粒体途径诱导细胞凋亡和上调 p53,来抑制 3D 球体模型和具有不同分子亚型的代表性细胞系(包括对 MAPKi 具有内在和获得性耐药的细胞系)中的黑色素瘤细胞生长。此外,自噬抑制增强了这些 PHB 配体的抗肿瘤功效。更重要的是,这些配体可以与 MAPKi 协同作用,更有效地抑制 BRAF 野生型和突变型黑色素瘤的细胞生长并克服耐药性。总之,靶向 PHBs 代表了一种非常有前途的黑色素瘤治疗策略,无论突变状态如何。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c095/10378173/aefa3e322cba/cells-12-01855-g001.jpg

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