Sun Chiang Wang, Willmon Candice, Wu Li-Chen, Knopick Peter, Thoerner Jutta, Vile Richard, Townes Tim M, Terman David S
Department of Biochemistry and Molecular Genetics, University of Alabama Medical School at Birmingham , Birmingham, AL , USA.
Department of Molecular Medicine, Mayo Clinic Foundation , Rochester, MN , USA.
Front Oncol. 2016 Jul 8;6:166. doi: 10.3389/fonc.2016.00166. eCollection 2016.
Insights from the study of cancer resistance in animals have led to the discovery of novel anticancer pathways and opened new venues for cancer prevention and treatment. Sickle cells (SSRBCs) from subjects with homozygous sickle cell anemia (SCA) have been shown to target hypoxic tumor niches, induce diffuse vaso-occlusion, and potentiate a tumoricidal response in a heme- and oxidant-dependent manner. These findings spawned the hypothesis that SSRBCs and the vasculopathic microenvironment of subjects with SCA might be inimical to tumor outgrowth and thereby constitute a natural antitumor defense. We therefore implanted the B16F10 melanoma into humanized hemoglobin SS knockin mice which exhibit the hematologic and vasculopathic sequelae of human SCA. Over the 31-day observation period, hemoglobin SS mice showed no significant melanoma outgrowth. By contrast, 68-100% of melanomas implanted in background and hemoglobin AA knockin control mice reached the tumor growth end point (p < 0.0001). SS knockin mice also exhibited established markers of underlying vasculopathy, e.g., chronic hemolysis (anemia, reticulocytosis) and vascular inflammation (leukocytosis) that differed significantly from all control groups. Genetic differences or normal AA gene knockin do not explain the impaired tumor outgrowth in SS knockin mice. These data point instead to the chronic pro-oxidative vasculopathic network in these mice as the predominant cause. In related studies, we demonstrate the ability of the sickle cell component of this system to function as a therapeutic vehicle in potentiating the oncolytic/vasculopathic effect of RNA reovirus. Sickle cells were shown to efficiently adsorb and transfer the virus to melanoma cells where it induced apoptosis even in the presence of anti-reovirus neutralizing antibodies. In vivo, SSRBCs along with their viral cargo rapidly targeted the tumor and initiated a tumoricidal response exceeding that of free virus and similarly loaded normal RBCs without toxicity. Collectively, these data unveil two hitherto unrecognized findings: hemoglobin SS knockin mice appear to present a natural barrier to melanoma tumorigenesis while SSRBCs demonstrate therapeutic function as a vehicle for enhancing the oncolytic effect of free reovirus against established melanoma.
对动物抗癌抗性的研究见解促成了新抗癌途径的发现,并为癌症预防和治疗开辟了新途径。来自纯合镰状细胞贫血(SCA)患者的镰状细胞(SSRBCs)已被证明可靶向缺氧肿瘤微环境,诱导弥漫性血管阻塞,并以血红素和氧化剂依赖性方式增强杀肿瘤反应。这些发现催生了一种假说,即SSRBCs和SCA患者的血管病变微环境可能对肿瘤生长不利,从而构成一种天然的抗肿瘤防御。因此,我们将B16F10黑色素瘤植入表现出人类SCA血液学和血管病变后遗症的人源化血红蛋白SS基因敲入小鼠体内。在31天的观察期内,血红蛋白SS小鼠的黑色素瘤没有明显生长。相比之下,植入背景小鼠和血红蛋白AA基因敲入对照小鼠的黑色素瘤有68%-100%达到肿瘤生长终点(p < 0.0001)。SS基因敲入小鼠还表现出潜在血管病变的既定标志物,例如慢性溶血(贫血、网织红细胞增多)和血管炎症(白细胞增多),这些与所有对照组有显著差异。基因差异或正常AA基因敲入并不能解释SS基因敲入小鼠肿瘤生长受损的原因。相反,这些数据表明这些小鼠中的慢性促氧化血管病变网络是主要原因。在相关研究中,我们证明了该系统的镰状细胞成分作为治疗载体增强RNA呼肠孤病毒溶瘤/血管病变作用的能力。镰状细胞被证明能有效地吸附病毒并将其转移到黑色素瘤细胞中,即使在存在抗呼肠孤病毒中和抗体的情况下,病毒也能诱导黑色素瘤细胞凋亡。在体内,SSRBCs及其携带的病毒迅速靶向肿瘤并引发杀肿瘤反应,超过游离病毒和同样携带病毒的正常RBCs,且无毒性。总体而言,这些数据揭示了两个迄今未被认识的发现:血红蛋白SS基因敲入小鼠似乎对黑色素瘤肿瘤发生构成天然屏障,而SSRBCs作为载体具有治疗功能,可增强游离呼肠孤病毒对已形成黑色素瘤的溶瘤作用。