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DESCRIPTION (provided by applicant): The myometrium plays a fundamental role in a variety of female reproductive events and has a significant impact on pregnancy outcome. The structural and functional abnormalities of myometrium can lead to reproductive disorders, such as implantation failure, preterm labor, and uterine rupture, some of which are severe causes of neonatal mortality and morbidity. Despite the long-recognized importance of myometrial function in pregnancy, key signaling pathways that control myometrial development and function are not well defined. Lack of this knowledge is partially due to the lack of an animal model with myometrial defects resulting from disruption of defined cell signaling pathways. This creates a significant barrier that prevents an effective therapeutic intervention for myometrial dysfunction. Our objective of this proposal is to define the role of transforming growth factor (TGF) signaling in myometrium, and identify the contribution of dysregulated TGF signaling to the development of uterine diseases. We hypothesize that TGF signaling is required for myometrial development and function, and dysregulated myometrial TGF signaling is linked to uterine diseases such as adenomyosis. We will test our hypothesis in two specific aims: 1) Identify the role of TGF signaling in myometrial contractility and pregnancy; and 2) Define the mechanistic contributions of dysregulated TGF signaling to the development of myometrial defects and uterine adenomyosis. To achieve these aims, we will use complementary approaches including a conditional knockout strategy and in vitro assays to test our working hypotheses. Successful completion of the proposed application will help to uncover the signaling pathways that control the structural and functional properties of the myometrium, and achieve a new paradigm for understanding the mechanisms underlying myometrial pathologies. These data could potentially guide the design of novel therapies for myometrial dysfunction and myometrium-associated diseases.
期刊论文(6)
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会议论文
DOI: 10.1186/2049-1891-5-52
发表时间: 2014
期刊: Journal of animal science and biotechnology
影响因子: 7
作者: [Li Q]
通讯作者: Li Q
Conditional abrogation of transforming growth factor-β receptor 1 in PTEN-inactivated endometrium promotes endometrial cancer progression in mice.
在PTEN灭活的子宫内膜中转化生长因子-β受体1的条件废除可促进小鼠的子宫内膜癌进展。
DOI: 10.1002/path.4930
发表时间: 2017-09
期刊: The Journal of pathology
影响因子: --
作者: [Gao Y, Lin P, Lydon JP, Li Q]
通讯作者: Li Q
UTX: A novel regulator of decidualization?
  • 批准号:
    10390537
  • 项目类别:
  • 资助金额:
    $7.3万
  • 财政年份:
    2022
  • 负责人:
    Qinglei Li
  • 依托单位:
UTX: A novel regulator of decidualization?
  • 批准号:
    10570990
  • 项目类别:
  • 资助金额:
    $7.29万
  • 财政年份:
    2022
  • 负责人:
    Qinglei Li
  • 依托单位:
A novel mouse model of testicular granulosa cell tumors
  • 批准号:
    10062490
  • 项目类别:
  • 资助金额:
    $7.31万
  • 财政年份:
    2019
  • 负责人:
    Qinglei Li
  • 依托单位:
TGF-BETA SIGNALING IN ENDOMETRIAL CELL FUNCTION AND DYSFUNCTION
  • 批准号:
    9886078
  • 项目类别:
  • 资助金额:
    $30.44万
  • 财政年份:
    2017
  • 负责人:
    Qinglei Li
  • 依托单位:
国内基金
海外基金
分化肌细胞脱细胞ECM-cells sheet 3D 支架构建及其促进容积性肌组织缺损再 生修复应用及机制研究
CAFs-TAMs-tumor cells调控在HRHPV感染致癌中的作用机制研究及AI可追溯预测模型建立
  • 批准号:
    82072862
  • 项目类别:
    面上项目
  • 资助金额:
    56.0万元
  • 批准年份:
    2020
  • 负责人:
    徐云升
  • 依托单位:
S100A8/A9--Myeloid cells特异性可溶性表氧化物水解酶(sEH)基因敲除改善胰岛素抵抗的新靶点
  • 批准号:
    82070825
  • 项目类别:
    面上项目
  • 资助金额:
    53.0万元
  • 批准年份:
    2020
  • 负责人:
    徐西振
  • 依托单位:
Leader cells通过CCL5调控糖酵解及基质硬度促进结直肠癌集体侵袭的 作用机制
  • 批准号:
    81903002
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.5万元
  • 批准年份:
    2019
  • 负责人:
    王斐斐
  • 依托单位: