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Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression

Endometriosis is a common gynecological disease defined as the growth of endometrial tissues outside the uterus. Although the mechanism underlying the progression of endometriosis has not been fully elucidated, cancer-like aerobic glycolysis is considered to mediate the elevated growth and resistanc...

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Autores principales: Kim, Bo-Sung, Chung, Tae-Wook, Choi, Hee-Jung, Bae, Sung-Jin, Cho, Hye-Rin, Lee, Syng-Ook, Choi, Jung-Hye, Joo, Jong Kil, Ha, Ki-Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903453/
https://www.ncbi.nlm.nih.gov/pubmed/33732330
http://dx.doi.org/10.3892/etm.2021.9788
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author Kim, Bo-Sung
Chung, Tae-Wook
Choi, Hee-Jung
Bae, Sung-Jin
Cho, Hye-Rin
Lee, Syng-Ook
Choi, Jung-Hye
Joo, Jong Kil
Ha, Ki-Tae
author_facet Kim, Bo-Sung
Chung, Tae-Wook
Choi, Hee-Jung
Bae, Sung-Jin
Cho, Hye-Rin
Lee, Syng-Ook
Choi, Jung-Hye
Joo, Jong Kil
Ha, Ki-Tae
author_sort Kim, Bo-Sung
collection PubMed
description Endometriosis is a common gynecological disease defined as the growth of endometrial tissues outside the uterus. Although the mechanism underlying the progression of endometriosis has not been fully elucidated, cancer-like aerobic glycolysis is considered to mediate the elevated growth and resistance to apoptosis of endometriotic cells. The heartwood of Caesalpinia sappan L. (family Leguminosae) is a herbal medicinal product used to treat gynecological symptoms, including algomenorrhea and amenorrhea. The results of the present study revealed that endometriotic 12Z cells exhibited more rapid growth than normal endometrial cells (THES). The expression levels of pyruvate dehydrogenase kinase (PDK)1 and 3 and lactate production were higher in 12Z cells than in THES cells. In addition, the 12Z cells were more sensitive to the cytotoxicity of the aqueous extract of C. sappan heartwood (CS) than the THES cells. CS inhibited lactate production and phosphorylation of pyruvate dehydrogenase A by reducing the expression of PDK1. CS also increased mitochondrial reactive oxygen species (ROS) levels, decreased mitochondrial membrane potential and consequently stimulated the apoptosis of 12Z cells. CS-induced cell death was substantially inhibited by exogenous PDK1 expression. In conclusion, CS may be a novel drug candidate for treating endometriosis by inhibiting aerobic glycolysis and inducing ROS-mitochondria-mediated apoptotic cell death.
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spelling pubmed-79034532021-03-16 Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression Kim, Bo-Sung Chung, Tae-Wook Choi, Hee-Jung Bae, Sung-Jin Cho, Hye-Rin Lee, Syng-Ook Choi, Jung-Hye Joo, Jong Kil Ha, Ki-Tae Exp Ther Med Articles Endometriosis is a common gynecological disease defined as the growth of endometrial tissues outside the uterus. Although the mechanism underlying the progression of endometriosis has not been fully elucidated, cancer-like aerobic glycolysis is considered to mediate the elevated growth and resistance to apoptosis of endometriotic cells. The heartwood of Caesalpinia sappan L. (family Leguminosae) is a herbal medicinal product used to treat gynecological symptoms, including algomenorrhea and amenorrhea. The results of the present study revealed that endometriotic 12Z cells exhibited more rapid growth than normal endometrial cells (THES). The expression levels of pyruvate dehydrogenase kinase (PDK)1 and 3 and lactate production were higher in 12Z cells than in THES cells. In addition, the 12Z cells were more sensitive to the cytotoxicity of the aqueous extract of C. sappan heartwood (CS) than the THES cells. CS inhibited lactate production and phosphorylation of pyruvate dehydrogenase A by reducing the expression of PDK1. CS also increased mitochondrial reactive oxygen species (ROS) levels, decreased mitochondrial membrane potential and consequently stimulated the apoptosis of 12Z cells. CS-induced cell death was substantially inhibited by exogenous PDK1 expression. In conclusion, CS may be a novel drug candidate for treating endometriosis by inhibiting aerobic glycolysis and inducing ROS-mitochondria-mediated apoptotic cell death. D.A. Spandidos 2021-04 2021-02-11 /pmc/articles/PMC7903453/ /pubmed/33732330 http://dx.doi.org/10.3892/etm.2021.9788 Text en Copyright: © Kim et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Kim, Bo-Sung
Chung, Tae-Wook
Choi, Hee-Jung
Bae, Sung-Jin
Cho, Hye-Rin
Lee, Syng-Ook
Choi, Jung-Hye
Joo, Jong Kil
Ha, Ki-Tae
Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression
title Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression
title_full Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression
title_fullStr Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression
title_full_unstemmed Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression
title_short Caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12Z cells through suppressing pyruvate dehydrogenase kinase 1 expression
title_sort caesalpinia sappan induces apoptotic cell death in ectopic endometrial 12z cells through suppressing pyruvate dehydrogenase kinase 1 expression
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903453/
https://www.ncbi.nlm.nih.gov/pubmed/33732330
http://dx.doi.org/10.3892/etm.2021.9788
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