Janes Peter W, Parslow Adam C, Cao Diana, Rigopoulos Angela, Lee Fook-Thean, Gong Sylvia J, Cartwright Glenn A, Burvenich Ingrid J G, Eriksson Ulf, Johns Terrance G, Scott Fiona E, Scott Andrew M
Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, VIC 3084, Australia.
School of Cancer Medicine, La Trobe University, Melbourne, VIC 3083, Australia.
Cancers (Basel). 2024 May 16;16(10):1902. doi: 10.3390/cancers16101902.
The vascular endothelial growth factors (VEGFs) and their receptors (VEGFRs) are key regulators of blood vessel formation, including in tumors, where their deregulated function can promote the production of aberrant, leaky blood vessels, supporting tumor development. Here we investigated the VEGFR1 ligand VEGF-B, which we demonstrate to be expressed in tumor cells and in tumor stroma and vasculature across a range of tumor types. We examined the anti-VEGF-B-specific monoclonal antibody 2H10 in preclinical xenograft models of breast and colorectal cancer, in comparison with the anti-VEGF-A antibody bevacizumab. Similar to bevacizumab, 2H10 therapy was associated with changes in tumor blood vessels and intra-tumoral diffusion consistent with normalization of the tumor vasculature. Accordingly, treatment resulted in partial inhibition of tumor growth, and significantly improved the response to chemotherapy. Our studies indicate the importance of VEGF-B in tumor growth, and the potential of specific anti-VEGF-B treatment to inhibit tumor development, alone or in combination with established chemotherapies.
血管内皮生长因子(VEGF)及其受体(VEGFR)是血管形成的关键调节因子,在肿瘤中也是如此,其功能失调可促进异常、渗漏血管的生成,从而支持肿瘤发展。在此,我们研究了VEGFR1配体VEGF-B,我们证明其在一系列肿瘤类型的肿瘤细胞、肿瘤基质和脉管系统中均有表达。我们在乳腺癌和结直肠癌的临床前异种移植模型中检测了抗VEGF-B特异性单克隆抗体2H10,并与抗VEGF-A抗体贝伐单抗进行了比较。与贝伐单抗相似,2H10治疗与肿瘤血管变化及瘤内扩散改变有关,这与肿瘤脉管系统正常化一致。因此,治疗导致肿瘤生长部分受抑,并显著改善了对化疗的反应。我们的研究表明VEGF-B在肿瘤生长中的重要性,以及特异性抗VEGF-B治疗单独或与既定化疗联合抑制肿瘤发展的潜力。