Regulation and Function of PTP-PEST in colon carcinoma

PTP-PEST在结肠癌中的调控及功能

• 批准号: 8014970
• 负责人: Sarita Kandula Sastry
• 金额: $ 27.83万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-05-01 至 2014-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8014970
• 关键词: Adherens Junction; Affect; Binding; Binding Proteins; Biochemical; Biological Markers; Cadherins; Cancer Center; Candidate Disease Gene; Cell-Cell Adhesion; Cells; Cellular biology; Colon Carcinoma; Contact Inhibition; Doctor of Philosophy; Ensure; Environment; Fibroblasts; Foundations; Future; Genes; Goals; Guanine Nucleotide Exchange Factors; Intercellular Junctions; Lead; Malignant Epithelial Cell; Malignant neoplasm of gastrointestinal tract; Medical; Mutate; Neoplasm Metastasis; PTPN12 gene; Phenotype; Protein Tyrosine Kinase; Protein Tyrosine Phosphatase; Proteins; Regulation; Research; Research Personnel; Signal Transduction; Site; Testing; Texas; Tumor Suppressor Proteins; Tyrosine; Tyrosine Phosphorylation; Universities; VAV2 gene; Work; anticancer research; base; cancer cell; catenin p120ctn protein; cell motility; effective therapy; functional loss; gene therapy; programs; rho GTP-Binding Proteins; success; tool; tumor progression

DESCRIPTION (provided by applicant): Protein tyrosine phosphatases (PTPases) are a largely understudied class of putative tumor suppressors. A critical step in tumor progression is the loss of cell-cell contacts leading to a highly invasive phenotype. Increased tyrosine kinase signaling at cell-cell contacts contributes to the invasion of colon carcinomas through disruption of adherens junctions. Cadherin engagement promotes cell-cell adhesion and contact inhibition of cell motility through regulation of Rho GTPases. p120 catenin is a tyrosine phosphorylated cadherin binding protein that regulates Rho GTPase activity. Binding of p120ctn to cadherins stabilizes adherens junctions. Elevated RTK signaling increases cytoplasmic p120ctn and leads to cell scattering and invasion by delocalizing Rho GTPase activity from adherens junctions to the leading edge. The delocalization of p120ctn is associated with aggressive colon cancer. However, the mechanisms that control tyrosine phosphorylation of p120ctn and how this affects junctional integrity, Rho GTPase activity and subsequent invasion of colon carcinoma cells are poorly understood. PTP-PEST is a cytoplasmic PTPase that, like p120ctn, regulates cell motility through Rho GTPases. Our preliminary evidence indicates that PTP-PEST targets p120ctn in colon carcinoma cells. In addition, the PTP-PEST gene is mutated in colon cancer cells leading to a loss of functional protein. How loss of PTP-PEST expression correlates with motility and Rho GTPase activity is not known. Our long-term goal is to understand how PTP-PEST contributes to colon cancer progression. The purpose of this proposal is to investigate how PTP-PEST controls Rho GTPase activity in adherens junctions to limit colon carcinoma invasion and how changes in PTP-PEST expression influence invasive potential. The specific aims of this proposal are: 1) Determine how localization of PTP-PEST affects integrity of adherens junctions and cell motility 2) Elucidate how PTP- PEST modulates Rac1 and RhoA activity downstream of cadherin engagement and 3) Examine how PTP- PEST expression affects the invasive and metastatic potential of colon carcinoma cells. A major barrier to effective treatment of colon cancer is a need for targeted therapies. Our work will establish PTP-PEST as a potential candidate for the treatment of colon cancer as a suppressor of invasion. Completion of the proposed aims will lead to a better understanding of the cellular and biochemical mechanisms by which PTP- PEST functions to control colon carcinoma invasion. Moreover, our studies will lay a foundation for future studies investigating PTP-PEST as a potential biomarker and as a candidate for gene therapy based approaches to circumvent colon carcinoma invasion.

描述（由申请人提供）：蛋白酪氨酸磷酸酶（PTPases）是一类研究不足的假定肿瘤抑制因子。肿瘤进展的关键步骤是细胞-细胞接触的丧失，导致高度侵袭性表型。细胞-细胞接触处增加的酪氨酸激酶信号通过破坏粘附连接促进结肠癌的侵袭。钙粘蛋白结合通过调节Rho GTP酶促进细胞-细胞粘附和细胞运动的接触抑制。p120连环蛋白是一种酪氨酸磷酸化钙粘蛋白结合蛋白，调节Rho GT3活性。p120 ctn与钙粘蛋白的结合使粘附连接稳定。升高的RTK信号增加细胞质p120 ctn，并通过使Rho GTdR活性从粘附连接处离域到前缘而导致细胞分散和侵袭。p120 ctn的非定位与侵袭性结肠癌相关。然而，控制p120 ctn的酪氨酸磷酸化的机制，以及这如何影响连接的完整性，Rho GT3活性和随后的结肠癌细胞的侵袭知之甚少。PTP-PEST是一种细胞质PTB，与p120 ctn一样，通过Rho GTPases调节细胞运动。我们的初步证据表明PTP-PEST靶向p120 ctn在结肠癌细胞。此外，PTP-PEST基因在结肠癌细胞中发生突变，导致功能性蛋白质的丧失。PTP-PEST表达的丧失如何与运动性和Rho GT3活性相关尚不清楚。我们的长期目标是了解PTP-PEST如何促进结肠癌进展。本研究的目的是探讨PTP-PEST如何控制粘附连接中Rho GT3的活性以限制结肠癌的侵袭，以及PTP-PEST表达的变化如何影响侵袭潜力。该提议的具体目的是：1）确定PTP-PEST的定位如何影响粘附连接的完整性和细胞运动性2）阐明PTP-PEST如何调节钙粘蛋白接合下游的Rac 1和RhoA活性和3）检查PTP-PEST表达如何影响结肠癌细胞的侵袭和转移潜力。有效治疗结肠癌的主要障碍是需要靶向治疗。我们的工作将建立PTP-PEST作为一个潜在的候选人治疗结肠癌作为一个抑制剂的侵袭。该目标的实现将有助于更好地理解PTP-PEST控制结肠癌侵袭的细胞和生化机制。此外，我们的研究将为未来研究PTP-PEST作为潜在的生物标志物和作为基于基因治疗的方法来规避结肠癌侵袭的候选者奠定基础。