Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin

Kazuhisa Kameyama,1,* Keiichi Motoyama,1,* Nao Tanaka,1 Yuki Yamashita,1 Taishi Higashi,1 Hidetoshi Arima1,2,* 1Department of Physical Pharmaceutics, Graduate School of Pharmaceutical Sciences, 2Program for Leading Graduate Schools “HIGO (Health Life Science: Interdisciplinary and Glocal...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Kameyama K, Motoyama K, Tanaka N, Yamashita Y, Higashi T, Arima H
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://doaj.org/article/6de3764b95d44cbeb4b1ea0ff8ee86a8
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:6de3764b95d44cbeb4b1ea0ff8ee86a8
record_format dspace
spelling oai:doaj.org-article:6de3764b95d44cbeb4b1ea0ff8ee86a82021-12-02T03:58:39ZInduction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin1178-2013https://doaj.org/article/6de3764b95d44cbeb4b1ea0ff8ee86a82017-04-01T00:00:00Zhttps://www.dovepress.com/induction-of-mitophagy-mediated-antitumor-activity-with-folate-appende-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Kazuhisa Kameyama,1,* Keiichi Motoyama,1,* Nao Tanaka,1 Yuki Yamashita,1 Taishi Higashi,1 Hidetoshi Arima1,2,* 1Department of Physical Pharmaceutics, Graduate School of Pharmaceutical Sciences, 2Program for Leading Graduate Schools “HIGO (Health Life Science: Interdisciplinary and Glocal Oriented) Program,” Kumamoto University, Kumamoto, Japan *These authors contributed equally to this work Abstract: Mitophagy is the specific autophagic elimination system of mitochondria, which regulates cellular survival via the removal of damaged mitochondria. Recently, we revealed that folate-appended methyl-β-cyclodextrin (FA-M-β-CyD) provides selective antitumor activity in folate receptor-α (FR-α)-expressing cells by the induction of autophagy. In this study, to gain insight into the detailed mechanism of this antitumor activity, we focused on the induction of mitophagy by the treatment of FR-α-expressing tumor cells with FA-M-β-CyD. In contrast to methyl-β-cyclodextrin, FA-M-β-CyD entered KB cells, human epithelial cells from a fatal cervical carcinoma (FR-α (+)) through FR-α-mediated endocytosis. The transmembrane potential of isolated mitochondria after treatment with FA-M-β-CyD was significantly elevated. In addition, FA-M-β-CyD lowered adenosine triphosphate (ATP) production and promoted reactive oxygen species production in KB cells (FR-α (+)). Importantly, FA-M-β-CyD enhanced light chain 3 (LC3) conversion (LC3-I to LC3-II) in KB cells (FR-α (+)) and induced PTEN-induced putative kinase 1 (PINK1) protein expression, which is involved in the induction of mitophagy. Furthermore, FA-M-β-CyD had potent antitumor activity in BALB/c nu/nu mice xenografted with KB cells (FR-α (+)) without any significant side effects. Taken together, these findings demonstrate that the autophagic cell death elicited by FA-M-β-CyD could be associated with mitophagy induced by an impaired mitochondrial function. Keywords: mitophagy, autophagy, folate receptor, methyl-β-cyclodextrin, tumor targetingKameyama KMotoyama KTanaka NYamashita YHigashi TArima HDove Medical Pressarticlemitophagyautophagyfolate receptormethyl--cyclodextrintumor targetingMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 3433-3446 (2017)
institution DOAJ
collection DOAJ
language EN
topic mitophagy
autophagy
folate receptor
methyl--cyclodextrin
tumor targeting
Medicine (General)
R5-920
spellingShingle mitophagy
autophagy
folate receptor
methyl--cyclodextrin
tumor targeting
Medicine (General)
R5-920
Kameyama K
Motoyama K
Tanaka N
Yamashita Y
Higashi T
Arima H
Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
description Kazuhisa Kameyama,1,* Keiichi Motoyama,1,* Nao Tanaka,1 Yuki Yamashita,1 Taishi Higashi,1 Hidetoshi Arima1,2,* 1Department of Physical Pharmaceutics, Graduate School of Pharmaceutical Sciences, 2Program for Leading Graduate Schools “HIGO (Health Life Science: Interdisciplinary and Glocal Oriented) Program,” Kumamoto University, Kumamoto, Japan *These authors contributed equally to this work Abstract: Mitophagy is the specific autophagic elimination system of mitochondria, which regulates cellular survival via the removal of damaged mitochondria. Recently, we revealed that folate-appended methyl-β-cyclodextrin (FA-M-β-CyD) provides selective antitumor activity in folate receptor-α (FR-α)-expressing cells by the induction of autophagy. In this study, to gain insight into the detailed mechanism of this antitumor activity, we focused on the induction of mitophagy by the treatment of FR-α-expressing tumor cells with FA-M-β-CyD. In contrast to methyl-β-cyclodextrin, FA-M-β-CyD entered KB cells, human epithelial cells from a fatal cervical carcinoma (FR-α (+)) through FR-α-mediated endocytosis. The transmembrane potential of isolated mitochondria after treatment with FA-M-β-CyD was significantly elevated. In addition, FA-M-β-CyD lowered adenosine triphosphate (ATP) production and promoted reactive oxygen species production in KB cells (FR-α (+)). Importantly, FA-M-β-CyD enhanced light chain 3 (LC3) conversion (LC3-I to LC3-II) in KB cells (FR-α (+)) and induced PTEN-induced putative kinase 1 (PINK1) protein expression, which is involved in the induction of mitophagy. Furthermore, FA-M-β-CyD had potent antitumor activity in BALB/c nu/nu mice xenografted with KB cells (FR-α (+)) without any significant side effects. Taken together, these findings demonstrate that the autophagic cell death elicited by FA-M-β-CyD could be associated with mitophagy induced by an impaired mitochondrial function. Keywords: mitophagy, autophagy, folate receptor, methyl-β-cyclodextrin, tumor targeting
format article
author Kameyama K
Motoyama K
Tanaka N
Yamashita Y
Higashi T
Arima H
author_facet Kameyama K
Motoyama K
Tanaka N
Yamashita Y
Higashi T
Arima H
author_sort Kameyama K
title Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
title_short Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
title_full Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
title_fullStr Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
title_full_unstemmed Induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
title_sort induction of mitophagy-mediated antitumor activity with folate-appended methyl-β-cyclodextrin
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/6de3764b95d44cbeb4b1ea0ff8ee86a8
work_keys_str_mv AT kameyamak inductionofmitophagymediatedantitumoractivitywithfolateappendedmethylbetacyclodextrin
AT motoyamak inductionofmitophagymediatedantitumoractivitywithfolateappendedmethylbetacyclodextrin
AT tanakan inductionofmitophagymediatedantitumoractivitywithfolateappendedmethylbetacyclodextrin
AT yamashitay inductionofmitophagymediatedantitumoractivitywithfolateappendedmethylbetacyclodextrin
AT higashit inductionofmitophagymediatedantitumoractivitywithfolateappendedmethylbetacyclodextrin
AT arimah inductionofmitophagymediatedantitumoractivitywithfolateappendedmethylbetacyclodextrin
_version_ 1718401494064037888