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中文摘要
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描述(由申请人提供):超过50%的男性癌症患者接受以顺铂为基础的化疗后会长期不育。这是一个重大问题,因为这些患者中有许多是儿童或年轻男性,他们在癌症中幸存下来,并希望以后再生。然而,目前还没有针对化疗引起的不孕症的药物治疗。顺铂诱导不孕症发生的关键因素是生殖细胞凋亡,促凋亡介质p53和核因子κ B (NF?B)与它的发展有牵连。生长素是一种新型激素,具有抗凋亡和抑制NF?B在其他组织中。我们的初步研究表明,它可以减少顺铂诱导的生殖细胞凋亡。然而,胃饥饿素在这种情况下的作用机制及其对生育的影响尚不清楚。这项应用的长期目标是:a)开发新的策略来保护暴露于化疗药物的个体的生育能力;b)建立在这种情况下调节胃饥饿素作用的机制。假设:我们假设胃饥饿素可以预防顺铂诱导的不孕症并下调睾丸NF?顺铂诱导的B和p53活化。我们的具体目的是:1)确定ghrelin给药对顺铂性不孕的影响;2)确定ghrelin和顺铂对睾丸p53和NF?B的活动。设计和方法:在我们的顺铂诱导性腺损伤的啮齿动物模型中,我们观察到胃饥饿素可以阻止顺铂诱导的睾丸细胞凋亡和NF?B激活。我们现在提议测试生长素和顺铂对生育能力、p53和NF?利用一种新的转基因小鼠系,在含有NF?的启动子控制下表达荧光素酶和绿色荧光蛋白。B共识结合位点。基于我们的成人模型中产生的数据,我们也将建立青春期前不孕症模型的可行性。意义:生育能力是超过80%的儿童和男性癌症化疗长期幸存者的主要生活方式。ghrelin对生殖能力、生殖细胞凋亡和NF?在这种情况下,B和p53的活性对于开发预防或逆转顺铂和其他化疗药物引起的不孕症的方法将是重要的。这种追求将与那些暴露于化疗药物、化学物质或辐射的男性保持长期生育能力有关。公共卫生相关性:很大一部分接受化疗治疗癌症的儿童和男子的生殖器官受到损害,导致不孕症。我们目前还没有办法预防或预测谁会在接受化疗后变得不孕;然而,我们的初步工作首次表明,一种名为“生长素”的新激素可以防止化疗对生殖器官的损害。我们在这里提出的实验将确定生长素对生育的影响,并将引导我们开发预防或治疗不孕症的新方法。
英文摘要
DESCRIPTION (provided by applicant): More than 50% of male cancer patients subjected to cisplatin-based chemotherapy will suffer from long-term infertility. This is a significant concern because many of these patients are children or young men who survive their cancer and would hope to later reproduce. However, medical treatment for chemotherapy-induced infertility is not currently available. A key factor in the development of cisplatin-induced infertility is germ cell apoptosis, and activation of the proapoptotic mediators p53 and Nuclear Factor kappa B (NF?B) has been implicated in its development. Ghrelin, a novel hormone, has anti-apoptotic properties and suppresses NF?B in other tissues. Our preliminary studies indicate that it reduces cisplatin-induced apoptosis in germ cells. However, ghrelin's mechanism(s) of action in this setting and its effect on fertility are unknown. The long-term objectives of this application are: a) to develop new strategies for preserving fertility in individuals exposed to chemotherapeutic drugs and b) to establish the mechanisms mediating ghrelin's effects in this setting. Hypothesis: We hypothesize that ghrelin will prevent cisplatin-induced infertility and downregulate testicular NF?B and p53 activation induced by cisplatin. Our specific aims are: 1) To determine the effect of ghrelin administration on cisplatin-induced infertility and 2) To establish the effects of ghrelin and cisplatin on testicular p53 and NF?B activity. Design and methods: In our rodent model of cisplatin-induced gonadal damage we have observed that ghrelin prevents cisplatin-induced testicular apoptosis and NF?B activation. We are now proposing to test the effects of ghrelin and cisplatin on fertility, p53 and NF?B activity by exploiting a new transgenic mouse line that has been engineered to express luciferase and green fluorescent protein under control of a promoter that contains NF?B consensus binding sites. Based on the data generated in our adult model, we also will establish the feasibility of a prepubertal model of infertility. Significance: Fertility is the major life-style concern in more than 80% of children and men who are long-term survivors of cancer chemotherapy. Establishing the mechanisms and effects of ghrelin on fertility, germ cell apoptosis and NF?B and p53 activity in this setting will be important to develop methods to prevent or reverse the infertility caused by cisplatin and other chemotherapeutic agents. Such a pursuit will have relevance for maintaining long-term fertility in men who are exposed to chemotherapeutic agents, chemicals or radiation. PUBLIC HEALTH RELEVANCE: A significant proportion of children and men receiving chemotherapy for the treatment of cancer suffer damage to their reproductive organs leading to infertility. We currently do not have a way to prevent or predict who will become infertile after receiving chemotherapy; however, our preliminary work shows for the first time that a new hormone called "ghrelin" prevents this damage to the reproductive organs due to chemotherapy. The experiments we propose here will determine the effects of ghrelin on fertility and will lead us to the development of new ways to prevent or treat infertility.
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The Role of Ghrelin and the GHSR-1a receptor in Sarcopenic Obesity
  • 批准号:
    10292456
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2015
  • 负责人:
    Jose M. Garcia
  • 依托单位:
The Role of Ghrelin and the GHSR-1a receptor in Sarcopenic Obesity
  • 批准号:
    9887510
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2015
  • 负责人:
    Jose M. Garcia
  • 依托单位:
The Role of Ghrelin and the GHSR-1a receptor in Sarcopenic Obesity
  • 批准号:
    10057224
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2015
  • 负责人:
    Jose M. Garcia
  • 依托单位:
Mechanisms of action of ghrelin in muscle and adipose tissue in cancer cachexia
  • 批准号:
    9301106
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2015
  • 负责人:
    Jose M. Garcia
  • 依托单位:
海外基金