Plumbagin suppresses tumor cell growth in oral squamous cell carcinoma cell lines

Objectives Plumbagin (PL), a naturally occurring quinoid, exerts antitumoral effects in diverse types of cancer cells. However, the effect of PL on tumor cell proliferation in oral squamous cell carcinoma (OSCC) remains poorly understood. In this study, we assessed the efficacy of PL, in human OSCC...

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Veröffentlicht in:Oral diseases 2015-05, Vol.21 (4), p.501-511
Hauptverfasser: Ono, T, Ota, A, Ito, K, Nakaoka, T, Karnan, S, Konishi, H, Furuhashi, A, Hayashi, T, Yamada, Y, Hosokawa, Y, Kazaoka, Y
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container_end_page 511
container_issue 4
container_start_page 501
container_title Oral diseases
container_volume 21
creator Ono, T
Ota, A
Ito, K
Nakaoka, T
Karnan, S
Konishi, H
Furuhashi, A
Hayashi, T
Yamada, Y
Hosokawa, Y
Kazaoka, Y
description Objectives Plumbagin (PL), a naturally occurring quinoid, exerts antitumoral effects in diverse types of cancer cells. However, the effect of PL on tumor cell proliferation in oral squamous cell carcinoma (OSCC) remains poorly understood. In this study, we assessed the efficacy of PL, in human OSCC cells. Methods The effect of PL on the cell growth and apoptosis of OSCC cell lines was evaluated using MTT and Annexin V assays, respectively. The effect of PL on mitochondrial membrane potential loss and reactive oxygen species (ROS) generation was evaluated using flow cytometry analysis. Results MTT assay showed that PL dose‐dependently suppressed OSCC cell growth, with IC50 values ranging from 3.87 to 14.6 μM. Flow cytometry analysis revealed that PL treatment resulted in a significant decrease in mitochondrial membrane potential and an increase in the number of apoptotic cells. Notably, ROS generation was significantly elevated after PL treatment. Furthermore, a ROS scavenger, N‐acetylcysteine (NAC), clearly suppressed the decrease in mitochondrial membrane potential, increase of caspase‐3/7 activity, and apoptosis after PL treatment. Conclusion This study provides the considerable evidence of the tumor‐suppressive effect of PL, thereby highlighting its therapeutic potential for OSCC treatment.
doi_str_mv 10.1111/odi.12310
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However, the effect of PL on tumor cell proliferation in oral squamous cell carcinoma (OSCC) remains poorly understood. In this study, we assessed the efficacy of PL, in human OSCC cells. Methods The effect of PL on the cell growth and apoptosis of OSCC cell lines was evaluated using MTT and Annexin V assays, respectively. The effect of PL on mitochondrial membrane potential loss and reactive oxygen species (ROS) generation was evaluated using flow cytometry analysis. Results MTT assay showed that PL dose‐dependently suppressed OSCC cell growth, with IC50 values ranging from 3.87 to 14.6 μM. Flow cytometry analysis revealed that PL treatment resulted in a significant decrease in mitochondrial membrane potential and an increase in the number of apoptotic cells. Notably, ROS generation was significantly elevated after PL treatment. Furthermore, a ROS scavenger, N‐acetylcysteine (NAC), clearly suppressed the decrease in mitochondrial membrane potential, increase of caspase‐3/7 activity, and apoptosis after PL treatment. Conclusion This study provides the considerable evidence of the tumor‐suppressive effect of PL, thereby highlighting its therapeutic potential for OSCC treatment.</description><identifier>ISSN: 1354-523X</identifier><identifier>EISSN: 1601-0825</identifier><identifier>DOI: 10.1111/odi.12310</identifier><identifier>PMID: 25580997</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>anti-cancer drug ; Antineoplastic Agents, Phytogenic - pharmacology ; Apoptosis ; Apoptosis - drug effects ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - pathology ; Cell Cycle - drug effects ; Cell growth ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Chemotherapy ; Dentistry ; Flow cytometry ; Humans ; Mouth Neoplasms - drug therapy ; Mouth Neoplasms - pathology ; Naphthoquinones - pharmacology ; Oral cancer ; oral squamous cell carcinoma ; plumbagin ; reactive oxygen species</subject><ispartof>Oral diseases, 2015-05, Vol.21 (4), p.501-511</ispartof><rights>2015 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2015 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2015 John Wiley &amp; Sons A/S. 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However, the effect of PL on tumor cell proliferation in oral squamous cell carcinoma (OSCC) remains poorly understood. In this study, we assessed the efficacy of PL, in human OSCC cells. Methods The effect of PL on the cell growth and apoptosis of OSCC cell lines was evaluated using MTT and Annexin V assays, respectively. The effect of PL on mitochondrial membrane potential loss and reactive oxygen species (ROS) generation was evaluated using flow cytometry analysis. Results MTT assay showed that PL dose‐dependently suppressed OSCC cell growth, with IC50 values ranging from 3.87 to 14.6 μM. Flow cytometry analysis revealed that PL treatment resulted in a significant decrease in mitochondrial membrane potential and an increase in the number of apoptotic cells. Notably, ROS generation was significantly elevated after PL treatment. Furthermore, a ROS scavenger, N‐acetylcysteine (NAC), clearly suppressed the decrease in mitochondrial membrane potential, increase of caspase‐3/7 activity, and apoptosis after PL treatment. Conclusion This study provides the considerable evidence of the tumor‐suppressive effect of PL, thereby highlighting its therapeutic potential for OSCC treatment.</description><subject>anti-cancer drug</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Cycle - drug effects</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Chemotherapy</subject><subject>Dentistry</subject><subject>Flow cytometry</subject><subject>Humans</subject><subject>Mouth Neoplasms - drug therapy</subject><subject>Mouth Neoplasms - pathology</subject><subject>Naphthoquinones - pharmacology</subject><subject>Oral cancer</subject><subject>oral squamous cell carcinoma</subject><subject>plumbagin</subject><subject>reactive oxygen species</subject><issn>1354-523X</issn><issn>1601-0825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1OwzAQhC0EglI48AIoEhc4BPwTx8kRChSkioIAtTfLcWwIJHFqJyp9e1wCHJDYy-5qvx2NBoADBE-RrzOTF6cIEwQ3wADFEIUwwXTTz4RGIcVkvgN2nXuDELGU4G2wgylNYJqyAXi4L7sqEy9FHbiuaaxyTrmg7SpjA6nKMnixZtm-Bv5urCgDt-hEZTrXH6WwsqhNJfq1LGrl9sCWFqVT-999CJ6vr55GN-FkOr4dnU9CSTGDYcZg7v1EuZY4yYmkmiqoIMMIZ4KhXGqEIgkjqWOtI5EwJgVSQqdKwDTHiAzBca_bWLPolGt5Vbi1DVErb5CjmEUYEoaZR4_-oG-ms7V3t6ZwEpMYU0-d9JS0xjmrNG9sUQm74gjydc7c58y_cvbs4bdil1Uq_yV_gvXAWQ8si1Kt_lfi08vbH8mw_yhcqz5-P4R95zEjjPLZ3ZjjRzqaTy5mPCWfhcSWTg</recordid><startdate>201505</startdate><enddate>201505</enddate><creator>Ono, T</creator><creator>Ota, A</creator><creator>Ito, K</creator><creator>Nakaoka, T</creator><creator>Karnan, S</creator><creator>Konishi, H</creator><creator>Furuhashi, A</creator><creator>Hayashi, T</creator><creator>Yamada, Y</creator><creator>Hosokawa, Y</creator><creator>Kazaoka, Y</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201505</creationdate><title>Plumbagin suppresses tumor cell growth in oral squamous cell carcinoma cell lines</title><author>Ono, T ; 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However, the effect of PL on tumor cell proliferation in oral squamous cell carcinoma (OSCC) remains poorly understood. In this study, we assessed the efficacy of PL, in human OSCC cells. Methods The effect of PL on the cell growth and apoptosis of OSCC cell lines was evaluated using MTT and Annexin V assays, respectively. The effect of PL on mitochondrial membrane potential loss and reactive oxygen species (ROS) generation was evaluated using flow cytometry analysis. Results MTT assay showed that PL dose‐dependently suppressed OSCC cell growth, with IC50 values ranging from 3.87 to 14.6 μM. Flow cytometry analysis revealed that PL treatment resulted in a significant decrease in mitochondrial membrane potential and an increase in the number of apoptotic cells. Notably, ROS generation was significantly elevated after PL treatment. 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subjects anti-cancer drug
Antineoplastic Agents, Phytogenic - pharmacology
Apoptosis
Apoptosis - drug effects
Carcinoma, Squamous Cell - drug therapy
Carcinoma, Squamous Cell - pathology
Cell Cycle - drug effects
Cell growth
Cell Line, Tumor
Cell Proliferation - drug effects
Chemotherapy
Dentistry
Flow cytometry
Humans
Mouth Neoplasms - drug therapy
Mouth Neoplasms - pathology
Naphthoquinones - pharmacology
Oral cancer
oral squamous cell carcinoma
plumbagin
reactive oxygen species
title Plumbagin suppresses tumor cell growth in oral squamous cell carcinoma cell lines
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