In vitro antitumor activity of the ethyl acetate extract of Potentilla chinensis in osteosarcoma cancer cells

The aim of the current study was to evaluate the anticancer effect of the ethanol extract of Potentilla chinensis, a Chinese medicinal plant. An MTT assay was used to evaluate the cell viability of MG-63 human osteosarcoma cancer cells and fR-2 cells. Furthermore, the effect of the extract on apopto...

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Veröffentlicht in:Molecular medicine reports 2016-10, Vol.14 (4), p.3634-3640
Hauptverfasser: Wan, Guang, Tao, Jin-Gang, Wang, Guo-Dong, Liu, Shen-Peng, Zhao, Hong-Xing, Liang, Qiu-Dong
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container_issue 4
container_start_page 3634
container_title Molecular medicine reports
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creator Wan, Guang
Tao, Jin-Gang
Wang, Guo-Dong
Liu, Shen-Peng
Zhao, Hong-Xing
Liang, Qiu-Dong
description The aim of the current study was to evaluate the anticancer effect of the ethanol extract of Potentilla chinensis, a Chinese medicinal plant. An MTT assay was used to evaluate the cell viability of MG-63 human osteosarcoma cancer cells and fR-2 cells. Furthermore, the effect of the extract on apoptosis induction, cell cycle phase distribution and inhibition of cell migration in the MG63 human osteosarcoma cancer cell line was evaluated. The effect of the extract on cell cycle phase distribution was assessed by flow cytometry using propidium iodide (PI). Phase contrast microscopy detected the morphological changes in MG63 cancer cells following extract treatment. The results of the study demonstrated that the extract was cytotoxic to MG63 cancer cells, while the normal cell line (epithelial cell line) showed lower susceptibility. Phase contrast microscopy showed distinguishing morphological features, such as cell shrinkage and blebbing induced by the extract treatment in osteosarcoma cancer cells. The average proportion of Annexin V-positive cells (total apoptotic cells) significantly increased from 5.6% in the control to 24.2, 38.8 and 55.7% in the 40, 80 and 150 µg/ml groups, respectively. The extract induced early and late apoptosis in the cancer cells. Flow cytometric analysis revealed that the extract induced G0/G1-cell cycle arrest, which also showed significant dose-dependence. The extract induced a significant and concentration-dependent reduction in cell migration. Moreover, DNA fragmentation was also examined by observation of the formation of DNA ladders. It was demonstrated that DNA fragmentation was increased with extract concentration compared with that in the control. Taken together, EEPC may serve as potential therapeutic agent against osteosarcoma, provided that the toxicity profile and in vivo investigations demonstrate that it is safe.
doi_str_mv 10.3892/mmr.2016.5679
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An MTT assay was used to evaluate the cell viability of MG-63 human osteosarcoma cancer cells and fR-2 cells. Furthermore, the effect of the extract on apoptosis induction, cell cycle phase distribution and inhibition of cell migration in the MG63 human osteosarcoma cancer cell line was evaluated. The effect of the extract on cell cycle phase distribution was assessed by flow cytometry using propidium iodide (PI). Phase contrast microscopy detected the morphological changes in MG63 cancer cells following extract treatment. The results of the study demonstrated that the extract was cytotoxic to MG63 cancer cells, while the normal cell line (epithelial cell line) showed lower susceptibility. Phase contrast microscopy showed distinguishing morphological features, such as cell shrinkage and blebbing induced by the extract treatment in osteosarcoma cancer cells. The average proportion of Annexin V-positive cells (total apoptotic cells) significantly increased from 5.6% in the control to 24.2, 38.8 and 55.7% in the 40, 80 and 150 µg/ml groups, respectively. The extract induced early and late apoptosis in the cancer cells. Flow cytometric analysis revealed that the extract induced G0/G1-cell cycle arrest, which also showed significant dose-dependence. The extract induced a significant and concentration-dependent reduction in cell migration. Moreover, DNA fragmentation was also examined by observation of the formation of DNA ladders. It was demonstrated that DNA fragmentation was increased with extract concentration compared with that in the control. Taken together, EEPC may serve as potential therapeutic agent against osteosarcoma, provided that the toxicity profile and in vivo investigations demonstrate that it is safe.</description><identifier>ISSN: 1791-2997</identifier><identifier>EISSN: 1791-3004</identifier><identifier>DOI: 10.3892/mmr.2016.5679</identifier><identifier>PMID: 27573158</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Acetates - chemistry ; Acetic acid ; Annexin V ; Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - pharmacology ; Antitumor activity ; Apoptosis ; Apoptosis - drug effects ; Bone cancer ; Bone Neoplasms - drug therapy ; Bone Neoplasms - pathology ; Cancer ; Cancer therapies ; Care and treatment ; Cell adhesion &amp; migration ; Cell cycle ; cell cycle arrest ; Cell Cycle Checkpoints - drug effects ; Cell Line, Tumor ; Cell migration ; Cell Movement - drug effects ; Chemotherapy ; Cytotoxicity ; Deoxyribonucleic acid ; DNA ; DNA damage ; DNA fragmentation ; Drug dosages ; Drugs, Chinese Herbal - chemistry ; Drugs, Chinese Herbal - pharmacology ; Ethanol ; Ethyl acetate ; Flow cytometry ; Health aspects ; Humans ; Materia medica, Vegetable ; Medicinal plants ; Microscopy ; Morphology ; Osteosarcoma ; Osteosarcoma - drug therapy ; Osteosarcoma - pathology ; Penicillin ; Plant extracts ; Potentilla ; Potentilla - chemistry ; Potentilla chinensis ; Propidium iodide ; Sarcoma ; Studies ; Toxicity</subject><ispartof>Molecular medicine reports, 2016-10, Vol.14 (4), p.3634-3640</ispartof><rights>Copyright: © Wan et al.</rights><rights>COPYRIGHT 2016 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2016</rights><rights>Copyright: © Wan et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-7908c5ab45a977be9f10596ca387dec671037e0e05b0606764130accc3a3aa263</citedby><cites>FETCH-LOGICAL-c514t-7908c5ab45a977be9f10596ca387dec671037e0e05b0606764130accc3a3aa263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,5556,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27573158$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wan, Guang</creatorcontrib><creatorcontrib>Tao, Jin-Gang</creatorcontrib><creatorcontrib>Wang, Guo-Dong</creatorcontrib><creatorcontrib>Liu, Shen-Peng</creatorcontrib><creatorcontrib>Zhao, Hong-Xing</creatorcontrib><creatorcontrib>Liang, Qiu-Dong</creatorcontrib><title>In vitro antitumor activity of the ethyl acetate extract of Potentilla chinensis in osteosarcoma cancer cells</title><title>Molecular medicine reports</title><addtitle>Mol Med Rep</addtitle><description>The aim of the current study was to evaluate the anticancer effect of the ethanol extract of Potentilla chinensis, a Chinese medicinal plant. An MTT assay was used to evaluate the cell viability of MG-63 human osteosarcoma cancer cells and fR-2 cells. Furthermore, the effect of the extract on apoptosis induction, cell cycle phase distribution and inhibition of cell migration in the MG63 human osteosarcoma cancer cell line was evaluated. The effect of the extract on cell cycle phase distribution was assessed by flow cytometry using propidium iodide (PI). Phase contrast microscopy detected the morphological changes in MG63 cancer cells following extract treatment. The results of the study demonstrated that the extract was cytotoxic to MG63 cancer cells, while the normal cell line (epithelial cell line) showed lower susceptibility. Phase contrast microscopy showed distinguishing morphological features, such as cell shrinkage and blebbing induced by the extract treatment in osteosarcoma cancer cells. The average proportion of Annexin V-positive cells (total apoptotic cells) significantly increased from 5.6% in the control to 24.2, 38.8 and 55.7% in the 40, 80 and 150 µg/ml groups, respectively. The extract induced early and late apoptosis in the cancer cells. Flow cytometric analysis revealed that the extract induced G0/G1-cell cycle arrest, which also showed significant dose-dependence. The extract induced a significant and concentration-dependent reduction in cell migration. Moreover, DNA fragmentation was also examined by observation of the formation of DNA ladders. It was demonstrated that DNA fragmentation was increased with extract concentration compared with that in the control. Taken together, EEPC may serve as potential therapeutic agent against osteosarcoma, provided that the toxicity profile and in vivo investigations demonstrate that it is safe.</description><subject>Acetates - chemistry</subject><subject>Acetic acid</subject><subject>Annexin V</subject><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Bone cancer</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - pathology</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Cell adhesion &amp; migration</subject><subject>Cell cycle</subject><subject>cell cycle arrest</subject><subject>Cell Cycle Checkpoints - drug effects</subject><subject>Cell Line, Tumor</subject><subject>Cell migration</subject><subject>Cell Movement - drug effects</subject><subject>Chemotherapy</subject><subject>Cytotoxicity</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA fragmentation</subject><subject>Drug dosages</subject><subject>Drugs, Chinese Herbal - chemistry</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Ethanol</subject><subject>Ethyl acetate</subject><subject>Flow cytometry</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Materia medica, Vegetable</subject><subject>Medicinal plants</subject><subject>Microscopy</subject><subject>Morphology</subject><subject>Osteosarcoma</subject><subject>Osteosarcoma - drug therapy</subject><subject>Osteosarcoma - pathology</subject><subject>Penicillin</subject><subject>Plant extracts</subject><subject>Potentilla</subject><subject>Potentilla - chemistry</subject><subject>Potentilla chinensis</subject><subject>Propidium iodide</subject><subject>Sarcoma</subject><subject>Studies</subject><subject>Toxicity</subject><issn>1791-2997</issn><issn>1791-3004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkk1v1DAQhiMEoqVw5IoicYBLFn87viBVFR-VKsEBztas43RdJfZie6vuv2eiXVYUIR9szzzz2mO_TfOakhXvDfswz3nFCFUrqbR50pxTbWjHCRFPj2tmjD5rXpRyR4iSTJrnzRnTUnMq-_Nmvo7tfag5tRBrqLs55RZcDRjbt2ls68a3vm72E0Z9hYq7h5qRWJLfU_VYNU3Quk2IPpZQ2hDbVKpPBbJLM2YgOp9b56epvGyejTAV_-o4XzQ_P3_6cfW1u_n25frq8qZzkoraaUN6J2EtJBit196MlEijHPBeD94pTQnXnngi10QRpZWgnIBzjgMHYIpfNB8PutvdevaDw1tmmOw2hxny3iYI9nEmho29TfdWEsF0r1Hg_VEgp187X6qdQ1lagOjTrljaMzyZEkYQffsPepd2OWJ7lhrOBP4BzifqFiZvQxzT8oqLqL0U2IE2Si33Xv2HwjH4ObgU_Rgw_qigOxS4nErJfjz1SIld_GHRH3bxh138gfybvx_mRP8xBALvDkDZQhzCkMqJQaWOio6Ijisu-G8nCcPJ</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Wan, Guang</creator><creator>Tao, Jin-Gang</creator><creator>Wang, Guo-Dong</creator><creator>Liu, Shen-Peng</creator><creator>Zhao, Hong-Xing</creator><creator>Liang, Qiu-Dong</creator><general>D.A. 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An MTT assay was used to evaluate the cell viability of MG-63 human osteosarcoma cancer cells and fR-2 cells. Furthermore, the effect of the extract on apoptosis induction, cell cycle phase distribution and inhibition of cell migration in the MG63 human osteosarcoma cancer cell line was evaluated. The effect of the extract on cell cycle phase distribution was assessed by flow cytometry using propidium iodide (PI). Phase contrast microscopy detected the morphological changes in MG63 cancer cells following extract treatment. The results of the study demonstrated that the extract was cytotoxic to MG63 cancer cells, while the normal cell line (epithelial cell line) showed lower susceptibility. Phase contrast microscopy showed distinguishing morphological features, such as cell shrinkage and blebbing induced by the extract treatment in osteosarcoma cancer cells. The average proportion of Annexin V-positive cells (total apoptotic cells) significantly increased from 5.6% in the control to 24.2, 38.8 and 55.7% in the 40, 80 and 150 µg/ml groups, respectively. The extract induced early and late apoptosis in the cancer cells. Flow cytometric analysis revealed that the extract induced G0/G1-cell cycle arrest, which also showed significant dose-dependence. The extract induced a significant and concentration-dependent reduction in cell migration. Moreover, DNA fragmentation was also examined by observation of the formation of DNA ladders. It was demonstrated that DNA fragmentation was increased with extract concentration compared with that in the control. Taken together, EEPC may serve as potential therapeutic agent against osteosarcoma, provided that the toxicity profile and in vivo investigations demonstrate that it is safe.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>27573158</pmid><doi>10.3892/mmr.2016.5679</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Acetates - chemistry
Acetic acid
Annexin V
Antineoplastic Agents, Phytogenic - chemistry
Antineoplastic Agents, Phytogenic - pharmacology
Antitumor activity
Apoptosis
Apoptosis - drug effects
Bone cancer
Bone Neoplasms - drug therapy
Bone Neoplasms - pathology
Cancer
Cancer therapies
Care and treatment
Cell adhesion & migration
Cell cycle
cell cycle arrest
Cell Cycle Checkpoints - drug effects
Cell Line, Tumor
Cell migration
Cell Movement - drug effects
Chemotherapy
Cytotoxicity
Deoxyribonucleic acid
DNA
DNA damage
DNA fragmentation
Drug dosages
Drugs, Chinese Herbal - chemistry
Drugs, Chinese Herbal - pharmacology
Ethanol
Ethyl acetate
Flow cytometry
Health aspects
Humans
Materia medica, Vegetable
Medicinal plants
Microscopy
Morphology
Osteosarcoma
Osteosarcoma - drug therapy
Osteosarcoma - pathology
Penicillin
Plant extracts
Potentilla
Potentilla - chemistry
Potentilla chinensis
Propidium iodide
Sarcoma
Studies
Toxicity
title In vitro antitumor activity of the ethyl acetate extract of Potentilla chinensis in osteosarcoma cancer cells
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