DEVELOPMENTAL CHANGES IN CORPUS LUTEUM

黄体的发育变化

• 批准号: 7381693
• 负责人: Carlos Marcelo Telleria
• 金额: $ 2.99万
• 依托单位: UNIVERSITY OF SOUTH DAKOTA
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-05-01 至 2007-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7381693
• 关键词: DEVELOPMENTAL; CHANGES; CORPUS; LUTEUM

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The major area of research undertaken in Dr. Telleria's laboratory deals with the molecular mechanisms by which steroid and peptide hormones control function, survival and physiological death (apoptosis) of ovarian cells. In vivo, ex-vivo and in-vitro experimental approaches are used combined with state-of-the-art techniques for the study of apoptosis and gene expression. The ultimate goal is to understand the mechanisms of ovarian cell death to be able to: i) reestablish function in cases of infertility caused by luteal dysfunction and corpus luteum inadequacy, in which the primary problem is the insufficient quantity or duration of progesterone secretion that leads to repetitive pregnancy losses; and ii) accelerate cell death in the case of ovarian cancer, which is the fourth most frequent cause of cancer death among women and the leading cause of death from gynecological malignancies.

该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者（PI）可能从另一个NIH来源获得主要资金，因此可以在其他CRISP条目中表示。所列机构为中心，不一定是研究者所在机构。Telleria博士实验室的主要研究领域涉及类固醇和肽类激素控制卵巢细胞功能、存活和生理死亡（凋亡）的分子机制。体内、离体和体外实验方法与最先进的技术相结合用于研究细胞凋亡和基因表达。最终目标是了解卵巢细胞死亡的机制，以便能够：i）在由黄体功能障碍和黄体不足引起的不孕症的情况下重建功能，其中主要问题是孕酮分泌的量或持续时间不足，导致重复妊娠损失;和ii）在卵巢癌的情况下加速细胞死亡，卵巢癌是妇女癌症死亡的第四大最常见原因，并且是妇科恶性肿瘤死亡的主要原因。