Division of Pediatrics, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Clin Cancer Res. 2010 Feb 1;16(3):848-56. doi: 10.1158/1078-0432.CCR-09-1299. Epub 2010 Jan 26.
Bone marrow (BM) cells contribute to tumor vessel formation that supports the growth of Ewing's sarcoma. These BM cells migrate into the tumor and differentiate into endothelial cells and pericytes. We investigated whether delta-like ligand 4 (DLL4) played a role in the formation of BM-derived pericytes/vascular smooth muscle cells (vSMC) during tumor vessel formation.
Using immunohistochemistry, we examined the expression pattern of DLL4 in 14 patient samples and two xenograft mouse models of Ewing's sarcoma. We then used intratumor injections of short hairpin RNA to inhibit DLL4 expression in Ewing's sarcoma tumors in mice, and evaluated the effect on BM-derived pericytes/vSMCs.
DLL4 was expressed by perivascular cells in 12 of 14 human samples and in BM-derived pericytes/vSMCs in both A4573 and TC71 xenograft tumors. Inhibition of DLL4 expression by short hairpin RNA correlated with the decreased numbers of BM-derived cells in tumor vessels and the decreased numbers of alpha-SMA(+), desmin(+), and NG2(+) pericytes/vSMCs, as well as increased tumor hypoxia.
DLL4 is important for the formation of BM-derived pericytes/vSMCs during vasculogenesis in Ewing's sarcoma. DLL4 may be a therapeutic target for treatment of Ewing's sarcoma by inhibition of blood vessel formation.
骨髓(BM)细胞有助于支持尤文肉瘤生长的肿瘤血管形成。这些 BM 细胞迁移到肿瘤中,并分化为内皮细胞和成纤维细胞。我们研究了在肿瘤血管形成过程中,delta 样配体 4(DLL4)是否在 BM 来源的周细胞/血管平滑肌细胞(vSMC)形成中发挥作用。
我们使用免疫组织化学方法检查了 DLL4 在 14 个人类样本和两种尤文肉瘤异种移植小鼠模型中的表达模式。然后,我们在小鼠的尤文肉瘤肿瘤中进行肿瘤内注射短发夹 RNA 以抑制 DLL4 的表达,并评估其对 BM 来源的周细胞/vSMC 的影响。
DLL4 在 14 个人类样本中的 12 个样本中和 A4573 和 TC71 异种移植肿瘤中的 BM 来源的周细胞/vSMC 中表达。短发夹 RNA 抑制 DLL4 的表达与肿瘤血管中 BM 来源细胞数量的减少以及 alpha-SMA(+)、结蛋白(+)和 NG2(+)周细胞/vSMC 的数量减少以及肿瘤缺氧增加相关。
DLL4 对于尤文肉瘤血管生成过程中 BM 来源的周细胞/vSMC 的形成是重要的。通过抑制血管形成,DLL4 可能成为治疗尤文肉瘤的治疗靶点。