Cysteine-rich angiogenic inducer 61 (CYR61), an angiogenic factor whose expression is decreased in fibroids. The aim of the present study was to determine if CYR61 secretion in smooth muscle cells (SMCs) is regulated by hypoxia and through the endothelin A (ETA) receptor. SMCs from fibroids (fSMC) and the adjacent myometrium smooth muscle cells (mSMCs) were extracted from ten women undergoing hysterectomy for uterine fibroids and cultured with or without 1.0 µM of an ETA receptor antagonist for 24 h under either normal or hypoxic oxygen conditions. Cellular secretion of endothelin-1 (ET-1) and CYR61 were measured via enzyme linked immunosorbent assay in the cell culture media. SMCs were collected to determine cell proliferation and CYR61 protein expression via Western blot. ET-1 secretion was significantly increased in fSMC and was decreased with blockade of the ETA receptor under both normoxia (P=0.0004) and hypoxia (P=0.008). CYR61 expression was decreased in fSMCs and significantly increased with blockade of the ETA receptor under hypoxia (P=0.04). Cell proliferation decreased with ETA blockade under normoxia (P=0.0001) and hypoxia (P=0.001). These results suggest that suppression of CYR61 secretion in fSMC is regulated by the ET-1 and that blockade with ETA could be considered for a future treatment option.
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October 2018
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Cover Image
In this issue, Wohlfahrtova et al. report on the link between early isolated v-lesion (eIV) and rejection of kidney allografts. The cover image is a Circos plot that depicts the association between the 15 most signifi cant up-regulated genes between TCMRV (T cell-mediated vascular rejection) and eIV, and signifi cantly enriched pathways and GO terms that play a role in the immune response. For further details, see pages 2269–2284 .
Research Article|
October 29 2018
Novel treatment avenues for uterine leiomyoma: a new implication for endothelin?
Kedra Wallace
;
1Department of Obstetrics & Gynecology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
Correspondence: Kedra Wallace ([email protected])
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Krystal Chatman;
Krystal Chatman
1Department of Obstetrics & Gynecology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
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Venessia Johnson;
Venessia Johnson
1Department of Obstetrics & Gynecology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
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Alexis Brookins;
Alexis Brookins
1Department of Obstetrics & Gynecology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
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John Rushing;
John Rushing
1Department of Obstetrics & Gynecology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
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Babbette LaMarca
Babbette LaMarca
1Department of Obstetrics & Gynecology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
2Department of Pharmacology & Toxicology, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216, U.S.A.
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Publisher: Portland Press Ltd
Received:
June 05 2018
Revision Received:
October 04 2018
Accepted:
October 08 2018
Accepted Manuscript online:
October 09 2018
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© 2018 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society
2018
Clin Sci (Lond) (2018) 132 (20): 2261–2267.
Article history
Received:
June 05 2018
Revision Received:
October 04 2018
Accepted:
October 08 2018
Accepted Manuscript online:
October 09 2018
Citation
Kedra Wallace, Krystal Chatman, Venessia Johnson, Alexis Brookins, John Rushing, Babbette LaMarca; Novel treatment avenues for uterine leiomyoma: a new implication for endothelin?. Clin Sci (Lond) 31 October 2018; 132 (20): 2261–2267. doi: https://doi.org/10.1042/CS20180474
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