Human Prostate Cancer Metastasis and Laminin Binding Integrins

人类前列腺癌转移和层粘连蛋白结合整合素

• 批准号: 8468666
• 负责人: ANNE E CRESS
• 金额: $ 29.26万
• 依托单位: UNIVERSITY OF ARIZONA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-26 至 2016-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8468666
• 关键词: Ablation; Adhesions; Antibodies; Archives; Biological Assay; Blocking Antibodies; Cancer Control; Cell Adhesion; Cells; Cessation of life; Clinical; Collaborations; Complex; Coupled; Development; Disease; Disease Progression; Epiphysial cartilage; Excision; Focal Adhesions; Genes; Goals; Human; Image; In Vitro; Injection of therapeutic agent; Integrin Binding; Integrins; Laminin; Ligand Binding Domain; Ligands; MSX1 gene; Malignant Neoplasms; Malignant neoplasm of prostate; Metastatic Lesion; Metastatic Neoplasm to the Bone; Methods; Molecular; Molecular and Cellular Biology; Morbidity - disease rate; Neoplasm Metastasis; Pain; Pathology; Patients; Peptides; Predisposition; Primary Lesion; Prostate; Prostatectomy; Prostatic Neoplasms; Proteolysis; Radiation therapy; Radiology Specialty; Recurrence; Recurrent disease; Residencies; Role; SCID Mice; Secondary to; Site; Source; Staging; Testing; Therapeutic; Translating; Variant; Work; Xenograft Model; Xenograft procedure; base; bone; cancer cell; cancer pain; cell motility; conventional therapy; digital; directed attention; genome wide association study; in vivo; inhibitor/antagonist; insight; migration; mimetics; mouse model; neoplastic cell; novel; novel therapeutics; prevent; prophylactic; receptor; skeletal; success; tissue culture; tumor

DESCRIPTION (provided by applicant): Our goal is to understand human prostate tumor cell adhesion, migration and to use this information to block subsequent aggressive spread to late stage secondary skeletal sites. Specifically, we will identify the role of laminin binding integrins A6B1, A6pB1 and A3B1 at the molecular and cellular level using both in vitro tissue culture and in vivo xenograft SCID mouse models. We will translate these findings to utilize blockers of integrin interactions and aggressive spread. Archived human prostate cancer bone metastases will validate key results. Several key observations have stimulated this work. First, laminin 511 binding integrins drive invasion and metastasis of human prostate cancer. They are persistently expressed in human prostate metastatic lesions, including bone. Recently, a laminin 511 receptor, A6 integrin, was 1 of 7 new prostate cancer susceptibility loci discovered in a genome-wide association study. Lastly, elevated expression of A6B1 is correlated with reduced patient survival in cancer. We and others have shown that blocking expression or function of A6B1 curtails invasion and metastasis of tumor cells both in vivo and in vitro. How they facilitate adhesion and migration, with subsequent metastasis and/or recurrent disease has yet to be fully elucidated. The central hypothesis is that laminin 511 adhesion and colonization of cancer cells in bone is dependent upon laminin binding integrins and regulated by novel pericellular proteolysis involving the uPA/uPAR axis. Early (and often clinically inapparent) bone metastasis can provide a sanctuary site for tumor cells. Deployment of tumor cells from bone via A6pB1 may explain the clinical reality of widespread skeletal recurrence as aggressive metastatic disease 5 to 10 years after primary therapy. If proven correct, this hypothesis could have important translational implications. The therapeutic strategy would consist of ablation of the primary lesion using radiotherapy and/or prostatectomy coupled with prophylactic anti-integrin antibodies or peptide combinations to eliminate osseous sanctuary sites, and thereby the potential source of late bone recurrence. This is a new concept of cancer control directed at adhesion dependent and bone resident cancer. We will test our central hypothesis by three specific aims using a combination of expertise including collaborations between experts in Molecular Cellular Biology, Pathology and Radiology. All aims contain functional endpoints of laminin 511 dependent adhesion and migration using in vitro tissue culture methods and in vivo assays, using an intra- osseous injection xenograft model, digital radiographs and quantitative micro CT imaging. Understanding the fundamental molecular basis of adhesion dependent sanctuary of tumor cells in bone and their subsequent deployment will lend novel insight into mechanisms controlling cancer cell migration and metastasis to secondary skeletal sites. Metastasis to secondary sites is a cause of skeletal morbidity, disease progression, cancer pain or death. Recurrent disease could be potentially eliminated by adding important "pre-emptive" strategies to conventional therapy.

描述（由申请人提供）：我们的目标是了解人前列腺肿瘤细胞的粘附、迁移，并利用这些信息阻断随后侵袭性扩散至晚期继发性骨骼部位。具体而言，我们将确定层粘连蛋白结合整合素A6 B1，A6 pB 1和A3 B1在分子和细胞水平上使用体外组织培养和体内异种移植物SCID小鼠模型的作用。我们将把这些发现转化为利用整合素相互作用和积极传播的阻断剂。存档的人前列腺癌骨转移将验证关键结果。几个关键的观察刺激了这项工作。首先，层粘连蛋白511结合整合素驱动人前列腺癌的侵袭和转移。它们在人前列腺转移性病变（包括骨）中持续表达。最近，层粘连蛋白511受体，A6整合素，是在全基因组关联研究中发现的7个新的前列腺癌易感性位点之一。最后，A6 B1的表达升高与癌症患者存活率降低相关。我们和其他人已经表明，阻断A6 B1的表达或功能可以在体内和体外减少肿瘤细胞的侵袭和转移。它们如何促进粘附和迁移，以及随后的转移和/或复发性疾病尚未完全阐明。核心假设是层粘连蛋白511粘附和骨中癌细胞的定植依赖于层粘连蛋白结合整联蛋白，并受涉及uPA/uPAR轴的新型细胞周蛋白水解调节。早期（通常临床上不明显）骨转移可以为肿瘤细胞提供庇护所。肿瘤细胞通过A6 pB 1从骨中的部署可能解释了在初次治疗后5至10年广泛骨骼复发作为侵袭性转移性疾病的临床现实。如果被证明是正确的，这一假设可能具有重要的翻译意义。治疗策略将包括使用放射治疗和/或直肠切除术消融原发性病变，结合预防性抗整联蛋白抗体或肽组合，以消除骨保护区部位，从而消除晚期骨复发的潜在来源。这是一种针对粘附依赖性和骨驻留性癌症的癌症控制新概念。我们将通过三个具体目标来测试我们的中心假设，这些目标使用专业知识的组合，包括分子细胞生物学，病理学和放射学专家之间的合作。所有目标均包含层粘连蛋白511依赖性粘附和迁移的功能终点，使用体外组织培养方法和体内测定，使用骨内注射异种移植模型、数字射线照片和定量显微CT成像。了解骨中肿瘤细胞的粘附依赖性避难所的基本分子基础及其随后的部署将为控制癌细胞迁移和转移到继发性骨骼部位的机制提供新的见解。转移到继发部位是骨骼发病、疾病进展、癌症疼痛或死亡的原因。通过在常规治疗中加入重要的“先发制人”策略，复发性疾病可能会被消除。