Mohamedali Khalid A, Poblenz Ann T, Sikes Charles R, Navone Nora M, Thorpe Philip E, Darnay Bryant G, Rosenblum Michael G
Department of Experimental Therapeutics and Genitourinary Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
Cancer Res. 2006 Nov 15;66(22):10919-28. doi: 10.1158/0008-5472.CAN-06-0459.
The pathophysiology of tumor growth following skeletal metastases and the poor response of this type of lesion to therapeutic intervention remains incompletely understood. Vascular endothelial growth factor (VEGF)-A and its receptors play a role in both osteoclastogenesis and tumor growth. Systemic (i.v.) treatment of nude mice bearing intrafemoral prostate (PC-3) tumors with the vascular ablative agent VEGF(121)/recombinant gelonin (rGel) strongly inhibited tumor growth. Fifty percent of treated animals had complete regression of bone tumors with no development of lytic bone lesions. Immunohistochemical analysis showed that VEGF(121)/rGel treatment suppressed tumor-mediated osteoclastogenesis in vivo. In vitro treatment of murine osteoclast precursors, both cell line (RAW264.7) and bone marrow-derived monocytes (BMM), revealed that VEGF(121)/rGel was selectively cytotoxic to osteoclast precursor cells rather than mature osteoclasts. VEGF(121)/rGel cytotoxicity was mediated by Flt-1, which was down-regulated during osteoclast differentiation. Analysis by flow cytometry and reverse transcription-PCR showed that both BMM and RAW264.7 cells display high levels of Flt-1 but low levels of Flk-1. Internalization of VEGF(121)/rGel into osteoclast precursor cells was suppressed by pretreatment with an Flt-1 neutralizing antibody or by placenta growth factor but not with an Flk-1 neutralizing antibody. Thus, VEGF(121)/rGel inhibits osteoclast maturation in vivo and it seems that this process is important in the resulting suppression of skeletal osteolytic lesions. This is a novel and unique mechanism of action for this class of agents and suggests a potentially new approach for treatment or prevention of tumor growth in bone.
骨骼转移后肿瘤生长的病理生理学以及这类病变对治疗干预反应不佳的情况仍未完全了解。血管内皮生长因子(VEGF)-A及其受体在破骨细胞生成和肿瘤生长中均发挥作用。用血管消融剂VEGF(121)/重组去糖链植物凝血素(rGel)对股骨内植入前列腺(PC-3)肿瘤的裸鼠进行全身(静脉内)治疗,可强烈抑制肿瘤生长。50%接受治疗的动物骨肿瘤完全消退,未出现溶骨性骨病变。免疫组织化学分析表明,VEGF(121)/rGel治疗在体内可抑制肿瘤介导的破骨细胞生成。对小鼠破骨细胞前体(细胞系RAW264.7和骨髓来源的单核细胞(BMM))进行体外治疗发现,VEGF(121)/rGel对破骨细胞前体细胞具有选择性细胞毒性,而非对成熟破骨细胞。VEGF(121)/rGel的细胞毒性由Flt-1介导,Flt-1在破骨细胞分化过程中表达下调。流式细胞术和逆转录PCR分析表明,BMM和RAW264.7细胞均高表达Flt-1但低表达Flk-1。用Flt-1中和抗体预处理或用胎盘生长因子可抑制VEGF(121)/rGel内化进入破骨细胞前体细胞,但用Flk-1中和抗体则无此作用。因此,VEGF(121)/rGel在体内可抑制破骨细胞成熟,而且这一过程似乎在最终抑制骨骼溶骨性病变中很重要。这是这类药物一种新颖独特的作用机制,提示了一种治疗或预防骨肿瘤生长的潜在新方法。