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Pentagamavunon-1 (PGV-1) inhibits ROS metabolic enzymes and suppresses tumor cell growth by inducing M phase (prometaphase) arrest and cell senescence

Identifieur interne : 000547 ( Main/Exploration ); précédent : 000546; suivant : 000548

Pentagamavunon-1 (PGV-1) inhibits ROS metabolic enzymes and suppresses tumor cell growth by inducing M phase (prometaphase) arrest and cell senescence

Auteurs : Beni Lestari [Japon] ; Ikuko Nakamae [Japon] ; Noriko Yoneda-Kato [Japon] ; Tsumoru Morimoto [Japon] ; Shigehiko Kanaya [Japon] ; Takashi Yokoyama [Japon] ; Masafumi Shionyu [Japon] ; Tsuyoshi Shirai [Japon] ; Edy Meiyanto [Indonésie] ; Jun-Ya Kato [Japon]

Source :

RBID : PMC:6795878

Abstract

We previously showed that curcumin, a phytopolyphenol found in turmeric (Curcuma longa), targets a series of enzymes in the ROS metabolic pathway, induces irreversible growth arrest, and causes apoptosis. In this study, we tested Pentagamavunon-1 (PGV-1), a molecule related to curcumin, for its inhibitory activity on tumor cells in vitro and in vivo. PGV-1 exhibited 60 times lower GI50 compared to that of curcumin in K562 cells, and inhibited the proliferation of cell lines derived from leukemia, breast adenocarcinoma, cervical cancer, uterine cancer, and pancreatic cancer. The inhibition of growth by PGV-1 remained after its removal from the medium, which suggests that PGV-1 irreversibly prevents proliferation. PGV-1 specifically induced prometaphase arrest in the M phase of the cell cycle, and efficiently induced cell senescence and cell death by increasing intracellular ROS levels through inhibition of ROS-metabolic enzymes. In a xenograft mouse model, PGV-1 had marked anti-tumor activity with little side effects by oral administration, whereas curcumin rarely inhibited tumor formation by this administration. Therefore, PGV-1 is a potential therapeutic to induce tumor cell apoptosis with few side effects and low risk of relapse.


Url:
DOI: 10.1038/s41598-019-51244-3
PubMed: 31619723
PubMed Central: 6795878


Affiliations:


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Le document en format XML

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<p id="Par1">We previously showed that curcumin, a phytopolyphenol found in turmeric (
<italic>Curcuma longa</italic>
), targets a series of enzymes in the ROS metabolic pathway, induces irreversible growth arrest, and causes apoptosis. In this study, we tested Pentagamavunon-1 (PGV-1), a molecule related to curcumin, for its inhibitory activity on tumor cells
<italic>in vitro</italic>
and
<italic>in vivo</italic>
. PGV-1 exhibited 60 times lower GI
<sub>50</sub>
compared to that of curcumin in K562 cells, and inhibited the proliferation of cell lines derived from leukemia, breast adenocarcinoma, cervical cancer, uterine cancer, and pancreatic cancer. The inhibition of growth by PGV-1 remained after its removal from the medium, which suggests that PGV-1 irreversibly prevents proliferation. PGV-1 specifically induced prometaphase arrest in the M phase of the cell cycle, and efficiently induced cell senescence and cell death by increasing intracellular ROS levels through inhibition of ROS-metabolic enzymes. In a xenograft mouse model, PGV-1 had marked anti-tumor activity with little side effects by oral administration, whereas curcumin rarely inhibited tumor formation by this administration. Therefore, PGV-1 is a potential therapeutic to induce tumor cell apoptosis with few side effects and low risk of relapse.</p>
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</TEI>
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<list>
<country>
<li>Indonésie</li>
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<name sortKey="Kanaya, Shigehiko" sort="Kanaya, Shigehiko" uniqKey="Kanaya S" first="Shigehiko" last="Kanaya">Shigehiko Kanaya</name>
<name sortKey="Kato, Jun Ya" sort="Kato, Jun Ya" uniqKey="Kato J" first="Jun-Ya" last="Kato">Jun-Ya Kato</name>
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<name sortKey="Yoneda Kato, Noriko" sort="Yoneda Kato, Noriko" uniqKey="Yoneda Kato N" first="Noriko" last="Yoneda-Kato">Noriko Yoneda-Kato</name>
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