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去整合素样蛋白策略抑制侵袭性三阴性乳腺癌。

Disintegrin-like Protein Strategy to Inhibit Aggressive Triple-Negative Breast Cancer.

机构信息

Laboratory of Biomolecules, Venoms and Theranostic Applications, LR20IPT01, Institut Pasteur of Tunis, Tunis El Manar University, Tunis 1068, Tunisia.

INSERM Unité 553, Laboratoire d'Hémostase, Endothélium et Angiogenèse, Hôpital Saint-Louis, 75010 Paris, France.

出版信息

Int J Mol Sci. 2023 Jul 30;24(15):12219. doi: 10.3390/ijms241512219.

Abstract

Venoms are a rich source of bioactive compounds, and among them is leberagin-C (Leb-C), a disintegrin-like protein derived from the venom of snakes. Leb-C has shown promising inhibitory effects on platelet aggregation. Previous studies have demonstrated that this SECD protein specifically targets α5β1, αvβ3, and αvβ6 integrins through a mimic mechanism of RGD disintegrins. In our current study, we focused on exploring the potential effects of Leb-C on metastatic breast cancer. Our findings revealed that Leb-C disrupted the adhesion, migration, and invasion capabilities of MDA-MB-231 breast cancer cells and its highly metastatic D3H2LN sub-population. Additionally, we observed significant suppression of adhesion, migration, and invasion of human umbilical vein endothelial cells (HUVECs). Furthermore, Leb-C demonstrated a strong inhibitory effect on fibroblast-growth-factor-2-induced proliferation of HUVEC. We conducted in vivo experiments using nude mice and found that treatment with 2 µM of Leb-C resulted in a remarkable 73% reduction in D3H2LN xenograft tumor size. Additionally, quantification of intratumor microvessels revealed a 50% reduction in tumor angiogenesis in xenograft after 21 days of twice-weekly treatment with 2 µM of Leb-C. Collectively, these findings suggest the potential utility of this disintegrin-like protein for inhibiting aggressive and resistant metastatic breast cancer.

摘要

毒液是生物活性化合物的丰富来源,其中包括 leberagin-C(Leb-C),一种源自蛇毒液的解整合素样蛋白。Leb-C 已显示出对血小板聚集具有有希望的抑制作用。先前的研究表明,这种 SECD 蛋白通过 RGD 解整合素的模拟机制特异性靶向 α5β1、αvβ3 和 αvβ6 整合素。在我们目前的研究中,我们专注于探索 Leb-C 对转移性乳腺癌的潜在影响。我们的研究结果表明,Leb-C 破坏了 MDA-MB-231 乳腺癌细胞及其高转移性 D3H2LN 亚群的粘附、迁移和侵袭能力。此外,我们观察到对人脐静脉内皮细胞(HUVEC)的粘附、迁移和侵袭的显著抑制。此外,Leb-C 对成纤维细胞生长因子-2 诱导的 HUVEC 增殖表现出强烈的抑制作用。我们使用裸鼠进行了体内实验,发现用 2µM 的 Leb-C 处理导致 D3H2LN 异种移植肿瘤大小显著减少 73%。此外,在 2µM 的 Leb-C 每周两次治疗 21 天后,对肿瘤内微血管的定量分析显示肿瘤血管生成减少了 50%。综上所述,这些发现表明这种解整合素样蛋白在抑制侵袭性和耐药性转移性乳腺癌方面具有潜在的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b5/10418936/21bb9c9d5515/ijms-24-12219-g001.jpg

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