Ruizhe Xu , Xiaomin Su , Xifeng Qin , Yue Liu , Jiayi Wu , Xuejing Li , Ting Wang , Xingyue Gong , Boshu Ouyang , Huiwen Liu , Wuli Yang , Jun Zhang , Bo Zhang , Zhiqing Pang
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引用次数: 0
Abstract
Combination therapy, as a vital strategy in cancer treatment, aims to overcome the limitations of monotherapies by combining two or more drugs or treatments to enhance antitumor efficacy. However, the unclear interactions between different therapies and the difficulty of precisely identifying effective combination treatments remain major challenges. In this study, we developed an omics-based drug-HIFU combination therapy discovery framework taking ferroptosis treatment of triple-negative breast cancer (TNBC) as a paradigm. Using the transcriptomics of a large TNBC cohort, drug sensitivity databases, and transcriptomics of high-intensity focused ultrasound (HIFU)-treated cells, the interaction network between HIFU, key ferroptosis genes, and potential drugs was constructed to predict and identify novel drugs that target ferroptosis and synergize with HIFU. It was found that 11 candidate ferroptosis drugs demonstrated synergistic cytotoxicity with HIFU in 4T1 cells, which lacked previous reports. Especially, HIFU, by upregulating IL-6 expression by 2.69-fold, reduced the IC50 of panobinostat in 4T1 cells by 5.27-fold. Panobinostat was subsequently loaded into platelet-mimicking liposomes (Pan-PML) for tumor targeted drug delivery to amplify the synergistic effect of panobinostat and HIFU. Importantly, the combination of HIFU and Pan-PML resulted in significant inhibition of tumor growth in the 4T1 tumor model, with 50 % of mice remaining free of tumor and lung metastasis compared to those treated with HIFU or Pan-PML alone. Mechanistically, it was discovered that Pan-PML, in combination with HIFU, significantly inhibited histone deacetylase (HDAC) activity to 1/50 of the original level and further reduced the expression of the ferroptosis-related gene SIRT3 to 19.17 % of baseline, thereby synergistically promoting ferroptosis in tumor cells and activating anti-tumor immunity. Thus, this omics-based drug-HIFU combination therapy discovery framework provides an innovative method to screen the combination therapy, which leverages the synergistic effects of existing drugs and HIFU and enables combination treatments to maximize antitumor efficacy.
期刊介绍:
Biomaterials is an international journal covering the science and clinical application of biomaterials. A biomaterial is now defined as a substance that has been engineered to take a form which, alone or as part of a complex system, is used to direct, by control of interactions with components of living systems, the course of any therapeutic or diagnostic procedure. It is the aim of the journal to provide a peer-reviewed forum for the publication of original papers and authoritative review and opinion papers dealing with the most important issues facing the use of biomaterials in clinical practice. The scope of the journal covers the wide range of physical, biological and chemical sciences that underpin the design of biomaterials and the clinical disciplines in which they are used. These sciences include polymer synthesis and characterization, drug and gene vector design, the biology of the host response, immunology and toxicology and self assembly at the nanoscale. Clinical applications include the therapies of medical technology and regenerative medicine in all clinical disciplines, and diagnostic systems that reply on innovative contrast and sensing agents. The journal is relevant to areas such as cancer diagnosis and therapy, implantable devices, drug delivery systems, gene vectors, bionanotechnology and tissue engineering.