DIETARY SOYBEAN COMPONENTS AFFECT ON PROSTATE CANCER PRO

膳食大豆成分对前列腺癌的影响

• 批准号: 2861895
• 负责人: JIN-RONG ZHOU
• 金额: $ 24.43万
• 依托单位: BETH ISRAEL DEACONESS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-06-01 至 2002-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/2861895
• 关键词: SCID mouse; androgens; angiogenesis; biomarker; cancer prevention; cell line; dietary supplements; genistein; immunocytochemistry; insulinlike growth factor; metalloendopeptidases; metastasis; neoplasm /cancer blood supply; neoplasm /cancer nutrition therapy; neoplastic growth; neoplastic process; nonhuman therapy evaluation; nutrition aspect of cancer; nutrition related tag; phytoestrogens; prostate neoplasms; soybeans; vascular endothelial growth factors

The long-term objective of this application is to test the hypothesis that soybeans bioactive components inhibit the growth and metastasis of prostate cancer (CaP). The specific aims are: 1) to evaluate the effects of soybean components on the growth and metastasis of an androgen-sensitive and PSA-producing human CaP cell line LNCaP, and an advanced and metastatic human CaP cell line PC-3 in vivo, and 2) To determine that soybean bioactive components inhibit the growth and metastasis of CaP tumors via inhibition of tumor angiogenesis. Male SCID mice will be inoculated intraprostatically with LNCaP or PC-3 cells, and assigned to one of the five soybean components-containing diets: 1) AIN-93M as control diet; 2) AIN-93 with isoflavone-depleted soy protein isolate, 3) AIN-93 with 0.7 percent of soy phytochemical concentrate, providing 800 mg genistein equivalents and 770mg daidzein equivalents/kg diet, 4) AIN-93 diet with 800mg genistein equivalents in the glycosylated form typically found in foods, or 5) AIN-93 diet with 770 mg daidzein equivalents/kg diet. At the end of experiment, primary tumor weight will be measured to determine prostatic tumor growth rate. We will quantitate the effects of dietary treatment on intraprostatic tumor growth and metastatic spread to the lymph nodes or lungs. We will first quantitate tumor proliferation index and apoptotic index which in prior studies show specific patterns of changes relative to microvessel density (factor VIII stainig). We will determine if VEGF, an angiogenic factor regulated by androgens and associated with prostate cancer progression, is inhibited by soy based diets. We will determine if circulating IGF-1 and androgens, both of which may modulate tumor angiogenesis and growth, are inhibited by soy treatments. Expression and activity of tumor metalloproteinases, critical regulators of tumor metastasis and angiogensis will be examined. Statistical analyses will be performed to answer the following questions: 1) if soy isoflavones are the major bioactive components inhibiting the growth and metastasis of prostate tumors; 2) if isoflavone-depleted soy protein has inhibitory effects on tumor growth and metastasis; 3) if other soybean phytochemicals have effects on tumor growth and metastasis; 4) if soybean bioactive components inhibit growth and/or metastasis of prostate tumors associated with regulations of angiogenesis-related biomarkers and/or other biomarkers. The proposed studies will provide new insight concerning the ability of bioactive components of soy to inhibit CaP progression. It is expencted that the results from proposed project will be translated to future clinical trials on CaP prevention/intervention.

本申请的长期目标是测试大豆生物活性成分抑制前列腺癌（CaP）的生长和转移的假设。 具体目标是：1）评价大豆组分对雄激素敏感的和产生PSA的人CaP细胞系LNCaP和晚期和转移性人CaP细胞系PC-3的体内生长和转移的影响，和2）确定大豆生物活性组分通过抑制肿瘤血管生成来抑制CaP肿瘤的生长和转移。 雄性SCID小鼠将前列腺内接种LNCaP或PC-3细胞，并分配至五种含大豆组分的饮食之一：1）AIN-93 M作为对照饮食; 3）AIN-93与0.7%的大豆植物化学浓缩物，提供800 mg染料木黄酮当量和770 mg大豆苷元当量/kg饮食，4）AIN-93饮食，其中800 mg染料木黄酮当量为通常在食物中发现的糖基化形式，或5）AIN-93饮食，其中770 mg大豆苷元当量/kg饮食。 在实验结束时，将测量原发性肿瘤重量以确定前列腺肿瘤生长速率。 我们将定量饮食治疗对前列腺内肿瘤生长和转移扩散到淋巴结或肺的影响。我们将首先定量肿瘤增殖指数和凋亡指数，这在先前的研究中显示了相对于微血管密度的特定变化模式（因子VIII染色）。 我们将确定是否VEGF，一种由雄激素调节的血管生成因子，与前列腺癌进展相关，被大豆为基础的饮食抑制。 我们将确定是否循环IGF-1和雄激素，这两者都可以调节肿瘤血管生成和生长，被大豆治疗抑制。 将检测肿瘤转移和血管生成的关键调节因子肿瘤金属蛋白酶的表达和活性。 通过统计分析回答以下问题：1）大豆异黄酮是否是抑制前列腺肿瘤生长和转移的主要生物活性成分; 2）去除异黄酮的大豆蛋白是否具有抑制肿瘤生长和转移的作用; 3）其他大豆植物化学物质是否具有抑制肿瘤生长和转移的作用; 4）大豆生物活性成分是否抑制与血管生成相关的生物标志物和/或其他生物标志物的调节相关的前列腺肿瘤的生长和/或转移。 拟议的研究将提供有关大豆生物活性成分抑制CaP进展的能力的新见解。 预计该项目的结果将转化为未来的CaP预防/干预临床试验。