Skp2 in androgen-dependent proliferation of prostate cancer cells

描述（由申请人提供）：前列腺癌已成为西方人群中最常见的男性癌症。前列腺癌通常以雄激素依赖性（AD）形式开始，雄激素消融术可以有效治疗。然而，雄激素消融治疗几乎总是导致更具侵袭性的雄激素非依赖型（AI）疾病。关于这一重要问题的大多数研究都集中在确定从AD到AI的疾病进展中的细胞和分子变化。在这个应用中，我们建议将重点放在了解雄激素-雄激素受体（AR）如何促进AD前列腺癌细胞的增殖。雄激素- ar促进AD前列腺癌细胞的增殖和分化。我们相信，更好地了解雄激素-AR如何促进AD前列腺癌细胞的增殖，将有助于如何特异性地靶向AR的增殖促进功能，从而可能导致不损害癌细胞分化的AD前列腺癌的新治疗方法。与雄激素消融术相比，雄激素消融术可以抑制AD前列腺癌细胞的增殖和分化，这将为治疗AD前列腺癌建立一个新的范例。由于AR的功能至少在一些雄激素非依赖性（AI）前列腺癌中被发现是重要的，因此针对AR的促增殖功能也将影响AI前列腺癌的治疗，这是目前无法治愈的。我们在本应用中需要验证的假设是，F-box蛋白Skp2是AR的一个重要下游效应蛋白，可以独立于AD和部分AI前列腺癌细胞的分化介导AD和部分AI前列腺癌细胞的增殖，特异性靶向Skp2代表了治疗AD和部分AI前列腺癌的一个新概念。在Specific Aim 1中，我们将确定AR对Skp2调控的分子机制。在Specific Aim 2中，我们将确定雄激素对人类AD前列腺癌异种移植物中Skp2的调控，并确定和比较去势和Skp2敲低对异种移植物肿瘤生长和复发的影响。最后，在Specific Aim 3中，我们将使用小鼠模型来确定Skp2在AR致癌水平诱导的前列腺上皮增殖和转化中的作用，AR是人类前列腺癌的一个可疑原因。

DESCRIPTION (provided by applicant): Prostate cancer has become the most common male cancer diagnosed in Western populations. Prostate cancer generally starts in an androgen-dependent (AD) form, which can be effectively treated with androgen ablation therapies. Androgen ablation therapies however almost always lead to more aggressive androgen-independent (AI) forms of the disease. Most research on this important issue has focused on identifying cellular and molecular changes in disease progression from AD to AI. In this application, we propose instead to focus on understanding how androgen-androgen receptor (AR) functions to promote proliferation of AD prostate cancer cells. Androgen-AR promotes both proliferation and differentiation of AD prostate cancer cells. We believe that a better understanding of how androgen-AR promotes proliferation of AD prostate cancer cells will shed light on how to specifically target the proliferation-promoting function of AR, which may lead to new treatment for AD prostate cancer that does not compromise cancer cell differentiation. This will establish a new paradigm of treating AD prostate cancer as compared to androgen ablation therapy, which inhibits both proliferation and differentiation of AD prostate cancer cells. Since functions of AR have been found important for at least some androgen-independent (AI) prostate cancer, targeting the proliferation-promoting functions of AR will impact on the treatment of AI prostate cancer as well, which is current incurable. Our hypothesis to be tested in this application is that the F-box protein Skp2 is an important downstream effector of AR in mediating proliferation of AD and some AI prostate cancer cells independently of their differentiation, and specifically targeting Skp2 represents a new concept in treatment of AD and some AI prostate cancer. In Specific Aim 1, we will determine the molecular mechanisms underlying the regulation of Skp2 by AR. In Specific Aim 2, we will determine the regulation of Skp2 by androgen in human AD prostate cancer xenografts and determine and compare the effects of castration and Skp2 knockdown on xenograft tumor growth and recurrence. Finally in Specific Aim 3, we will use mouse models to determine the role of Skp2 in prostate epithelium proliferation and transformation induced by oncogenic levels of AR, which is a suspected cause of prostate cancer in humans. PUBLIC HEALTH RELEVANCE: Prostate cancer has become the most common male cancer diagnosed in Western populations. A fundamental property of prostate cancer is its initial androgen-dependence and inevitable progression to lethal androgen-independent forms of the disease. This project aims to understand how the androgen receptor promotes prostate cancer and to develop targeted treatment strategy for prostate cancer.