Keller Evan T
Department of Urology, University of Michigan, 1500 E. Medical Center Dr., Room 5308 CCGCB, Ann Arbor, MI 48105.
For Immunopathol Dis Therap. 2011;2(1):89-94. doi: 10.1615/ForumImmunDisTher.v2.i1.
Raf kinase inhibitor protein (RKIP) is a small, cytosolic protein named for its ability to block Raf-mediated activation of MAPK and ERK. It also block G-protein signaling and NF-κB activation. An in vitro screen to identify genes that regulate prostate cancer (PCa) metastasis revealed that expression of RKIP was decreased in high versus low metastatic PCa cells. Modulation of RKIP expression revealed that it inhibited invasion and loss of RKIP promoted in vitro invasion. Animal studies were used to demonstrate that RKIP could inhibit PCa metastasis from orthotopically injected tumor cells without an effect on primary tumor growth. Taken together, these results indicated RKIP acted as a PCa metastasis suppressor gene. Evaluation of RKIP expression in clinical cases of PCa revealed that RKIP expression was moderate to high in non-neoplastic prostate, low in 50% of primary prostate cancers, and absent to low in the majority of metastases. Furthermore, low RKIP expression in primary prostate tumors was predictive of early tumor recurrence. Loss of RKIP was shown to induce resistance to radiation in PCa cells in vitro and in an in vivo murine model. Taken together, these studies indicate that RKIP plays multiple roles in PCa pathophysiology, suggesting that a method to increase RKIP expression in PCa may have therapeutic benefits.
Raf激酶抑制蛋白(RKIP)是一种小分子胞质蛋白,因其能够阻断Raf介导的MAPK和ERK激活而得名。它还能阻断G蛋白信号传导和NF-κB激活。一项旨在鉴定调控前列腺癌(PCa)转移基因的体外筛选显示,高转移与低转移PCa细胞中RKIP的表达均降低。对RKIP表达的调控表明,它能抑制侵袭,而RKIP的缺失则会促进体外侵袭。动物研究表明,RKIP可以抑制原位注射肿瘤细胞引起的PCa转移,而对原发性肿瘤生长没有影响。综上所述,这些结果表明RKIP作为一种PCa转移抑制基因发挥作用。对PCa临床病例中RKIP表达情况进行评估发现,RKIP在非肿瘤性前列腺组织中表达为中度至高度,在50%的原发性前列腺癌中表达较低,而在大多数转移灶中表达缺失或较低。此外,原发性前列腺肿瘤中RKIP低表达预示着肿瘤早期复发。在体外PCa细胞和体内小鼠模型中均显示,RKIP的缺失会诱导对辐射的抗性。综上所述,这些研究表明RKIP在PCa病理生理学中发挥多种作用,这表明一种增加PCa中RKIP表达的方法可能具有治疗益处。