Control of Medulloblastoma Migration & Survival by Unc5c

控制髓母细胞瘤迁移

• 批准号: 8269524
• 负责人: Robert J. Wechsler-Reya
• 金额: $ 4.78万
• 依托单位: SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-01 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8269524
• 关键词: Control; Medulloblastoma; Migration; Survival; Unc5c

DESCRIPTION (provided by applicant): Medulloblastoma is the most common malignant brain tumor in children. Its rapid growth and tendency to spread through the nervous system make it extremely difficult to treat, and more than 40% of the children who develop the disease die from it. Improved treatment of medulloblastoma is likely to come from a deeper understanding of the signals that control normal cerebellar development, and an appreciation of how these signals are dysregulated in tumors. To identify such signals, we have studied an animal model of medulloblastoma - the patched mutant mouse - and identified genes whose expression is altered in tumor cells compared to granule cell precursors (GCPs), the cells from which the tumor is believed to arise. Among the genes whose expression decreased most significantly was Unc5c, which encodes a receptor for the netrin family of signaling molecules. Unc5c was originally described as a regulator of cell migration, but has recently been shown to play an important role in apoptosis as well. Moreover, Unc5c is deleted or mutated in a variety of cancers, and has therefore been suggested to function as a tumor suppressor. We hypothesize that Unc5c controls migration and survival of GCPs during normal cerebellar development, and that its loss contributes to the abnormal migration and increased survival observed in medulloblastoma. If this hypothesis is correct, it will have important implications for our understanding of medulloblastoma, and open up new avenues for treatment of the disease. To test our hypothesis, we propose to: 1) Determine whether Unc5c regulates inward migration of granule cell precursors and tumor cells 2) Test whether Unc5c regulates survival of granule cell precursors and tumor cells 3) Determine whether loss of Unc5c is required for medulloblastoma formation Relevance to Public Health: One of the greatest challenges in medulloblastoma treatment is the ability of tumor cells to migrate into regions where they would not normally go, and to survive once they get there. Our observation of altered Unc5c expression in medulloblastoma is significant because it can contribute to both of these behaviors. By elucidating the role of Unc5c in migration and survival, our studies will shed light on the molecular mechanisms that underlie the aggressive growth and dissemination of medulloblastoma. This, in turn, will pave the way for developing new treatments that can be used to fight this devastating disease.

描述（由申请人提供）：髓母细胞瘤是儿童中最常见的恶性脑肿瘤。神经管母细胞瘤是一种神经系统疾病，它的生长速度快，易于通过神经系统扩散，因此治疗非常困难，超过40%的儿童死于这种疾病。神经管母细胞瘤的治疗方法的改进可能来自于对控制正常小脑发育的信号的更深入的理解，以及对这些信号在肿瘤中是如何失调的理解。为了识别这些信号，我们研究了髓母细胞瘤的动物模型-补丁突变小鼠-并确定了与颗粒细胞前体（GCPs）相比，肿瘤细胞中表达发生改变的基因，肿瘤被认为是由颗粒细胞前体（GCPs）引起的。其中表达下降最显著的基因是Unc 5c，它编码netrin家族信号分子的受体。Unc 5c最初被描述为细胞迁移的调节剂，但最近已被证明在凋亡中也起重要作用。此外，Unc 5c在多种癌症中缺失或突变，因此被认为是肿瘤抑制因子。我们推测Unc 5c在正常小脑发育过程中控制着GCPs的迁移和存活，其缺失导致了在髓母细胞瘤中观察到的异常迁移和存活增加。如果这一假设是正确的，它将对我们理解髓母细胞瘤有重要意义，并为治疗该病开辟新的途径。为了验证我们的假设，我们建议：1）确定Unc 5c是否调节颗粒细胞前体细胞和肿瘤细胞的向内迁移2）测试Unc 5c是否调节颗粒细胞前体细胞和肿瘤细胞的存活3）确定Unc 5c的缺失是否是髓母细胞瘤形成所必需的。髓母细胞瘤治疗中最大的挑战之一是肿瘤细胞迁移到它们通常不会去的区域的能力，并且一旦它们到达那里就能够存活。我们在髓母细胞瘤中观察到Unc 5c表达的改变是有意义的，因为它可以促进这两种行为。通过阐明Unc 5c在迁移和生存中的作用，我们的研究将揭示髓母细胞瘤侵袭性生长和播散的分子机制。反过来，这将为开发可用于对抗这种毁灭性疾病的新疗法铺平道路。

项目成果

Identification of CD15 as a marker for tumor-propagating cells in a mouse model of medulloblastoma.

• DOI: 10.1016/j.ccr.2008.12.016
• 发表时间: 2009-02-03
• 期刊: Cancer cell
• 影响因子: 50.3
• 作者: Read TA;Fogarty MP;Markant SL;McLendon RE;Wei Z;Ellison DW;Febbo PG;Wechsler-Reya RJ
• 通讯作者: Wechsler-Reya RJ

Medulloblastoma can be initiated by deletion of Patched in lineage-restricted progenitors or stem cells.

• DOI: 10.1016/j.ccr.2008.07.003
• 发表时间: 2008-08-12
• 期刊: Cancer cell
• 影响因子: 50.3
• 作者: Yang ZJ;Ellis T;Markant SL;Read TA;Kessler JD;Bourboulas M;Schüller U;Machold R;Fishell G;Rowitch DH;Wainwright BJ;Wechsler-Reya RJ
• 通讯作者: Wechsler-Reya RJ

Targeting sonic hedgehog-associated medulloblastoma through inhibition of Aurora and Polo-like kinases.

• DOI: 10.1158/0008-5472.can-12-4258
• 发表时间: 2013-10-15
• 期刊: Cancer research
• 影响因子: 11.2
• 作者: Markant SL;Esparza LA;Sun J;Barton KL;McCoig LM;Grant GA;Crawford JR;Levy ML;Northcott PA;Shih D;Remke M;Taylor MD;Wechsler-Reya RJ
• 通讯作者: Wechsler-Reya RJ