A novel recombinant attenuated Salmonella carrying RGD and melittin genes induces apoptosis of B16 cells and inhibits melanoma growth
文献类型： 外文期刊
作者： Li, Xin 1 ; Wu, Jingqiao 1 ; Meng, Jiali 1 ; Gao, Keke 1 ; Wang, Xiaoyue 1 ; Lan, Zhaoyu 1 ; Zhang, Dongchao 1 ; Jin, Tianming 1 ;
作者机构： 1.Tianjin Agr Univ, Coll Anim Sci & Vet Med, Tianjin Key Lab Agr Anim Breeding & Hlth Husb, 22 Jinjing Rd, Tianjin 300392, Peoples R China
2.Tianjin Acad Agr Sci, Inst Anim Sci & Vet, Tianjin Key Lab Anim Mol Breeding & Biotechnol, Tianjin 300381, Peoples R China
3.Shenyang Agr Univ, Coll Anim Sci & Vet Med, Shenyang 110866, Peoples R China
4.Tianjin Med Univ, Basic Med Coll, Tianjin 300070, Peoples R China
5.Capital Med Univ, Beijing Anzhen Hosp, Beijing Inst Heart Lung & Blood Vessel Dis, Beijing 100029, Peoples R China
6.Qitai Cty Anim Dis Prevent & Control Ctr, Changji 831800, Peoples R China
7.Tangshan Acad Agr Sci, Anim Husb & Vet Res Inst, Tangshan 063001, Peoples R China
8.Tianjin Ringpu Biotechnol Co Ltd, Tianjin 300308, Peoples R China
关键词： Melanoma; Arg-gly-asp; Melittin; salmonella; Targeted therapy
期刊名称：EUROPEAN JOURNAL OF PHARMACOLOGY （ 影响因子：4.7； 五年影响因子：4.7 ）
ISSN： 0014-2999
年卷期： 2025 年 1003 卷
页码：
收录情况： SCI
摘要： The tumor provides a favorable microenvironment for the growth of anaerobes and facultative anaerobes, such as Salmonella. Melittin (MEL) is a major component of bee venom that has a distinct inhibitory effect on tumor cell metastasis and invasion, but its clinical application is limited owing to non-specific cytotoxicity. Arg-Gly-Asp (RGD) is a potent competitive antagonist of extracellular matrix binding to alpha v beta 3, and is often used as a tumortargeting marker. Here, we engineered Salmonella typhimurium to selectively express and release RGD-MEL. The engineered bacteria were intratumourally injected into mice bearing B16 melanoma xenografts. We observed that RGD-mediated expression and release of MEL by S. Typhimurium promoted apoptosis while inhibiting B16 cell proliferation, migration, chemotaxis, and invasion. LH430/pRGD-MEL also had a prominent inhibitory effect on solid tumors. By leveraging the combined mechanisms of RGD and S. Typhimurium, LH430/pRGD-MEL demonstrates enhanced accumulation and expression within tumor tissues. Furthermore, no signs of tumor cell metastasis or noticeable lesions were observed in the liver and lungs. Notably, the mice treated with LH430/ pRGD-MEL exhibited significantly prolonged survival. RNA sequencing analysis revealed that engineered S. Typhimurium primarily disrupted the immune barrier within tumor tissue and inhibited tumor growth by upregulating apoptosis and phagocytosis-related pathways. These results indicate that LH430/pRGD-MEL demonstrates strong tumor-targeting capacity, minimizes host toxicity, and exhibits significant tumorsuppressive effects by promoting tumor cell apoptosis, highlighting the translational potential of microbialmediated precision oncology strategies.
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