Sleeping Beauty-Mediated microRNA Therapeutics for Metastatic Colorectal Cancer

描述（由申请人提供）：结直肠癌是全球癌症死亡的主要原因之一，肝脏是结直肠癌转移发展的最常见和关键部位。对于转移到肝脏的疾病患者，手术切除仍然是唯一的治愈希望。然而，这些患者中有85%不适合进行切除，其中结肠癌患者的5年生存率为0- 5%。MicroRNA（miRNAs）是长度约20个核苷酸的非编码RNA，其通过结合主要位于其mRNA靶的3 'UTR内的不完全互补位点来发挥其调节作用。它们在促进肿瘤发生、侵袭和转移中的因果作用只是最近才被发现。几乎所有的癌症类型都显示出miRNA的异常表达，在肿瘤细胞中具有过表达或更常见的低表达模式。我们假设这些miRNAs构成了发展抗转移性疾病分子疗法的有效靶点。在这里，我们建议使用睡美人转座子系统，以实现延长和高水平的肝脏定向表达的肿瘤抑制miRNAs以及针对致癌miRNAs的antimiRs在治疗转移到肝脏的人结直肠癌。虽然已经确定miRNA可以通过许多不同的机制水平转移，但缺乏在癌症动物模型中证明外源性miRNA从正常细胞转移到肿瘤细胞的体内数据。在目标1中，我们设计了一种方法来定量评估从正常肝组织到人肿瘤异种移植物的miRNA的细胞间转移，通过对肿瘤中荧光素酶报告基因表达的影响来测定miRNA向mRNA靶的递送。在目标2中，我们将测试肿瘤抑制性miRNA（miR-34 a、miR-9）以及靶向致癌性miRNA（miR-21）单独和组合针对裸鼠中的人结肠直肠肿瘤异种移植物的有效性。这些研究的结果将为在转移性疾病的体内模型中将治疗性microRNA从正常组织转移到肿瘤细胞中提供基本的实验支持。他们还将为基于miRNA的抗转移性结直肠癌的抗肿瘤策略提供临床前支持，该策略可能适用于治疗转移到肝脏的癌症。

DESCRIPTION (provided by applicant): Colorectal cancer is one of the leading causes of cancer death worldwide, with the liver being the most common and critical site for development of colorectal cancer metastases. Surgical resection remains the only curative hope for patients with disease that is metastatic to the liver. However, 85% of these patients are ineligible for resection, with the 5-year survival for inoperative patients ranging from 0-5%. MicroRNAs (miRNAs) are non-coding RNAs approximately 20 nucleotides in length that exert their regulatory effects by binding to imperfect complementary sites predominantly located within the 3'UTR of their mRNA targets. Their causal role in promoting tumorigenesis, invasion and metastases has only recently come to light. Almost all cancer types show aberrant expression of miRNAs, with patterns of overexpression or, more commonly, underexpression in tumor cells. We hypothesize that these miRNAs constitute valid targets for the development of molecular therapies against metastatic disease. Here we propose to use the Sleeping Beauty transposon system to achieve extended and high level liver-directed expression of both tumor suppressor miRNAs as well as antimiRs against oncogenic miRNAs in the treatment of human colorectal cancer metastatic to the liver. Although it is well established that miRNAs can be transferred horizontally by a number of different mechanisms, in vivo data demonstrating exogenous miRNA transfer from normal cells to tumor cells in an animal model of cancer are lacking. In Aim 1, we have devised an approach to quantitatively evaluate intercellular transfer of miRNA from normal liver tissue into human tumor xenografts, assaying for miRNA delivery to an mRNA target by the effect on luciferase reporter gene expression in tumors. In Aim 2 we will test the effectiveness of tumor suppressive miRNAs (miR-34a, miR-9) as well as targeting an oncogenic miRNA (miR-21) both singly and in combination against human colorectal tumor xenografts in nude mice. Results from these studies will provide fundamental experimental support for therapeutic microRNA transfer from normal tissues into tumor cells in an in vivo model of metastatic disease. They will also provide preclinical support for an miRNA-based antitumor strategy against metastatic colorectal cancer that is potentially applicable to the treatment of an cancer that is metastatic to the liver.