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Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines

PURPOSE: This study aimed to investigate whether Müllerian inhibiting substance (MIS) in combination with calcitriol modulates proliferation and apoptosis of human ovarian cancer (OCa) cell lines (SKOV3, OVCAR3, and OVCA433) and identify the signaling pathway by which MIS mediates apoptosis. MATERIA...

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Autores principales: Jung, Yeon Soo, Kim, Hee Jung, Seo, Seok Kyo, Choi, Young Sik, Nam, Eun Ji, Kim, Sunghoon, Kim, Sang Wun, Han, Hyuck Dong, Kim, Jae Wook, Kim, Young Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696969/
https://www.ncbi.nlm.nih.gov/pubmed/26632380
http://dx.doi.org/10.3349/ymj.2016.57.1.33
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author Jung, Yeon Soo
Kim, Hee Jung
Seo, Seok Kyo
Choi, Young Sik
Nam, Eun Ji
Kim, Sunghoon
Kim, Sang Wun
Han, Hyuck Dong
Kim, Jae Wook
Kim, Young Tae
author_facet Jung, Yeon Soo
Kim, Hee Jung
Seo, Seok Kyo
Choi, Young Sik
Nam, Eun Ji
Kim, Sunghoon
Kim, Sang Wun
Han, Hyuck Dong
Kim, Jae Wook
Kim, Young Tae
author_sort Jung, Yeon Soo
collection PubMed
description PURPOSE: This study aimed to investigate whether Müllerian inhibiting substance (MIS) in combination with calcitriol modulates proliferation and apoptosis of human ovarian cancer (OCa) cell lines (SKOV3, OVCAR3, and OVCA433) and identify the signaling pathway by which MIS mediates apoptosis. MATERIALS AND METHODS: OCa cell lines were treated with MIS in the absence or presence of calcitriol. Cell viability and proliferation were evaluated using the Cell Counting Kit-8 assay and apoptosis was evaluated by DNA fragmentation assay. Western blot and enzyme-linked immunosorbent assay were used to determine the signaling pathway. RESULTS: The cells showed specific staining for the MIS type II receptor. Treatment of OCa cells with MIS and calcitriol led to dose- and time-dependent inhibition of cell growth and survival. The combination treatment significantly suppressed cell growth, down-regulated the expression of B-cell lymphoma 2 (Bcl-2), and up-regulated the expressions of Bcl-2 associated X protein, caspase-3, and caspase-9 through the extracellular signal-regulated kinase signaling pathway. CONCLUSION: These results, coupled with a much-needed decrease in the toxic side effects of currently employed therapeutic agents, provide a strong rationale for testing the therapeutic potential of MIS, alone or in combination with calcitriol, in the treatment of OCa.
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spelling pubmed-46969692016-01-04 Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines Jung, Yeon Soo Kim, Hee Jung Seo, Seok Kyo Choi, Young Sik Nam, Eun Ji Kim, Sunghoon Kim, Sang Wun Han, Hyuck Dong Kim, Jae Wook Kim, Young Tae Yonsei Med J Original Article PURPOSE: This study aimed to investigate whether Müllerian inhibiting substance (MIS) in combination with calcitriol modulates proliferation and apoptosis of human ovarian cancer (OCa) cell lines (SKOV3, OVCAR3, and OVCA433) and identify the signaling pathway by which MIS mediates apoptosis. MATERIALS AND METHODS: OCa cell lines were treated with MIS in the absence or presence of calcitriol. Cell viability and proliferation were evaluated using the Cell Counting Kit-8 assay and apoptosis was evaluated by DNA fragmentation assay. Western blot and enzyme-linked immunosorbent assay were used to determine the signaling pathway. RESULTS: The cells showed specific staining for the MIS type II receptor. Treatment of OCa cells with MIS and calcitriol led to dose- and time-dependent inhibition of cell growth and survival. The combination treatment significantly suppressed cell growth, down-regulated the expression of B-cell lymphoma 2 (Bcl-2), and up-regulated the expressions of Bcl-2 associated X protein, caspase-3, and caspase-9 through the extracellular signal-regulated kinase signaling pathway. CONCLUSION: These results, coupled with a much-needed decrease in the toxic side effects of currently employed therapeutic agents, provide a strong rationale for testing the therapeutic potential of MIS, alone or in combination with calcitriol, in the treatment of OCa. Yonsei University College of Medicine 2016-01-01 2015-11-30 /pmc/articles/PMC4696969/ /pubmed/26632380 http://dx.doi.org/10.3349/ymj.2016.57.1.33 Text en © Copyright: Yonsei University College of Medicine 2016 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jung, Yeon Soo
Kim, Hee Jung
Seo, Seok Kyo
Choi, Young Sik
Nam, Eun Ji
Kim, Sunghoon
Kim, Sang Wun
Han, Hyuck Dong
Kim, Jae Wook
Kim, Young Tae
Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines
title Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines
title_full Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines
title_fullStr Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines
title_full_unstemmed Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines
title_short Anti-Proliferative and Apoptotic Activities of Müllerian Inhibiting Substance Combined with Calcitriol in Ovarian Cancer Cell Lines
title_sort anti-proliferative and apoptotic activities of müllerian inhibiting substance combined with calcitriol in ovarian cancer cell lines
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696969/
https://www.ncbi.nlm.nih.gov/pubmed/26632380
http://dx.doi.org/10.3349/ymj.2016.57.1.33
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