Hypoxia and the endometrium: An indispensable role for HIF-1α as therapeutic strategies

被引:3
|
作者
Dai, Wanlin [1 ]
Guo, Renhao [1 ]
Na, Xinni [2 ]
Jiang, Shuyi [1 ]
Liang, Junzhi [1 ]
Guo, Cuishan [2 ]
Fang, Yuanyuan [1 ,3 ]
Na, Zhijing [1 ,3 ]
Li, Da [1 ,3 ,4 ]
机构
[1] China Med Univ, Shengjing Hosp, Ctr Reprod Med, Dept Obstet & Gynecol, Shenyang, Peoples R China
[2] China Med Univ, Shengjing Hosp, Dept Obstet & Gynecol, Shenyang, Peoples R China
[3] China Med Univ, Natl Hlth Commiss, NHC Key Lab Adv Reprod Med & Fertil, Shenyang, Peoples R China
[4] Key Lab Reprod Dysfunct Dis & Fertil Remodeling Li, Shenyang, Peoples R China
来源
REDOX BIOLOGY | 2024年 / 73卷
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hypoxia; HIF-1; alpha; Endometrium; Menstruation; Decidualization; Endometrial diseases; ENDOTHELIAL GROWTH-FACTOR; INDUCIBLE FACTOR-I; DNA TOPOISOMERASE-I; STROMAL CELLS; ASHERMANS-SYNDROME; SIGNALING PATHWAY; FACTOR; 1-ALPHA; PHASE-I; EXPRESSION; FACTOR-1-ALPHA;
D O I
10.1016/j.redox.2024.103205
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypoxia-inducible factor 1 alpha (HIF-1 alpha) is a major molecular mediator of the hypoxic response. In the endometrium, local hypoxic conditions induced by hormonal fluctuations and endometrial vascular remodeling contribute to the production of HIF-1 alpha, which plays an indispensable role in a series of physiological activities, such as menstruation and metamorphosis. The sensitive regulation of HIF-1 alpha maintains the cellular viability and regenerative capacity of the endometrium against cellular stresses induced by hypoxia and excess reactive oxygen species. In contrast, abnormal HIF-1 alpha levels exacerbate the development of various endometrial pathologies. This knowledge opens important possibilities for the development of promising HIF-1 alpha-centered strategies to ameliorate endometrial disease. Nonetheless, additional efforts are required to elucidate the regulatory network of endometrial HIF-1 alpha and promote the applications of HIF-1 alpha-centered strategies in the human endometrium. Here, we summarize the role of the HIF-1 alpha-mediated pathway in endometrial physiology and pathology, highlight the latest HIF-1 alpha-centered strategies for treating endometrial diseases, and improve endometrial receptivity.
引用
收藏
页数:15
相关论文
共 50 条
  • [1] Crustacean responses to hypoxia:: The role of HIF-1α.
    Head, JM
    Terwilliger, NB
    INTEGRATIVE AND COMPARATIVE BIOLOGY, 2005, 45 (06) : 1010 - 1010
  • [2] Novel Therapeutic Targets for Hypoxia-Related Cardiovascular Diseases: The Role of HIF-1
    Liu, Minxuan
    Galli, Gina
    Wang, Yilin
    Fan, Qiru
    Wang, Zhenzhong
    Wang, Xin
    Xiao, Wei
    FRONTIERS IN PHYSIOLOGY, 2020, 11
  • [3] Cancer Cell Metabolism in Hypoxia: Role of HIF-1 as Key Regulator and Therapeutic Target
    Infantino, Vittoria
    Santarsiero, Anna
    Convertini, Paolo
    Todisco, Simona
    Iacobazzi, Vito
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (11)
  • [4] Development of novel therapeutic strategies that target HIF-1
    Semenza, GL
    EXPERT OPINION ON THERAPEUTIC TARGETS, 2006, 10 (02) : 267 - 280
  • [5] Harnessing the response to tissue hypoxia -: HIF-1α and therapeutic angiogenesis
    Vincent, KA
    Feron, O
    Kelly, RA
    TRENDS IN CARDIOVASCULAR MEDICINE, 2002, 12 (08) : 362 - 367
  • [6] The role of hypoxia inducible factor 1 (HIF-1) in hypoxia induced apoptosis
    Greijer, AE
    van der Wall, E
    JOURNAL OF CLINICAL PATHOLOGY, 2004, 57 (10) : 1009 - 1014
  • [7] Hypoxia-induced activation of HIF-1, role of HIF-1α-Hsp90 interaction
    Minet, E
    Mottet, D
    Michel, G
    Roland, I
    Raes, M
    Remacle, J
    Michiels, C
    FEBS LETTERS, 1999, 460 (02) : 251 - 256
  • [8] Hypoxia and HIF-1α in chondrogenesis
    Schipani, E
    SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (4-5) : 539 - 546
  • [9] Hypoxia and HIF-1α in osteoarthritis
    Pfander, D
    Cramer, T
    Swoboda, B
    INTERNATIONAL ORTHOPAEDICS, 2005, 29 (01) : 6 - 9
  • [10] Hypoxia, HIF-1, and cancer
    Semenza, G. L.
    CLINICAL & EXPERIMENTAL METASTASIS, 2008, 25 : 20 - 20