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Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells
Pancreatic ductal adenocarcinoma (PDAC) is highly aggressive disease and current treatment regimens fail to effectively cure PDAC. Development of resistance to current therapy is one of the key reasons for this outcome. Nimbolide (NL), a triterpenoid obtained from Azadirachta indica, exhibits antica...
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Published in: | Cancer letters 2018-01, Vol.413, p.82-93 |
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container_title | Cancer letters |
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creator | Kumar, Sandeep Inigo, Joseph R. Kumar, Rahul Chaudhary, Ajay K. O'Malley, Jordan Balachandar, Srimmitha Wang, Jianmin Attwood, Kristopher Yadav, Neelu Hochwald, Steven Wang, Xinjiang Chandra, Dhyan |
description | Pancreatic ductal adenocarcinoma (PDAC) is highly aggressive disease and current treatment regimens fail to effectively cure PDAC. Development of resistance to current therapy is one of the key reasons for this outcome. Nimbolide (NL), a triterpenoid obtained from Azadirachta indica, exhibits anticancer properties in various cancer including PDAC cells. However, the underlying mechanism of this anticancer agent in PDAC cells remains undefined. We show that NL exerts a higher level of apoptotic cell death compared to the first-line agent gemcitabine for PDAC, as well as other anticancer agents including sorafenib and curcumin. The anticancer efficacy of NL was further evidenced by a reduction in the CD44+ as well as cancer stem-like cell (CSC) population, as it causes decreased sphere formation. Mechanistically, the anticancer efficacy of NL associates with reduced mutant p53 as well as increased mitochondrial activity in the form of increased mitochondrial reactive oxygen species and mitochondrial mass. Together, this study highlights the therapeutic potential of NL in mutant p53 expressing pancreatic cancer.
•Nimbolide is a more effective caspase activator compared to gemcitabine.•Nimbolide treatment depletes CD44+ population in pancreatic cancer cells.•Nimbolide-induced apoptosis associates with increased mitochondrial activity.•Reduced levels of mutant p53 may contribute to anticancer effects of nimbolide. |
doi_str_mv | 10.1016/j.canlet.2017.10.029 |
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•Nimbolide is a more effective caspase activator compared to gemcitabine.•Nimbolide treatment depletes CD44+ population in pancreatic cancer cells.•Nimbolide-induced apoptosis associates with increased mitochondrial activity.•Reduced levels of mutant p53 may contribute to anticancer effects of nimbolide.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2017.10.029</identifier><identifier>PMID: 29107110</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Adenocarcinoma ; Antineoplastic Agents, Phytogenic - pharmacology ; Antitumor agents ; Apoptosis ; Apoptosis - drug effects ; Cancer stem cells ; Cancer therapies ; Carcinoma, Pancreatic Ductal - drug therapy ; Carcinoma, Pancreatic Ductal - genetics ; Carcinoma, Pancreatic Ductal - metabolism ; Carcinoma, Pancreatic Ductal - pathology ; Caspase Inhibitors - pharmacology ; CD44 antigen ; Cell death ; Cell Line, Tumor ; Cell Movement - drug effects ; Cells ; Chemotherapy ; Curcumin ; Deoxycytidine - analogs & derivatives ; Deoxycytidine - pharmacology ; Disease ; Dose-Response Relationship, Drug ; Gemcitabine ; Growth factors ; Humans ; Hyaluronan Receptors - metabolism ; Immunoglobulins ; Kinases ; Life sciences ; Limonins - pharmacology ; Medical treatment ; Metastasis ; Mitochondria ; Mitochondria - drug effects ; Mitochondria - metabolism ; Mitochondria - pathology ; Mutant p53 ; Mutation ; Neoplastic Stem Cells - drug effects ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Nimbolide ; p53 Protein ; Pancreatic cancer ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology ; Penicillin ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Thyroid cancer ; Time Factors ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>Cancer letters, 2018-01, Vol.413, p.82-93</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Limited Jan 28, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3</citedby><cites>FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3</cites><orcidid>0000-0001-7272-9384</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29107110$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, Sandeep</creatorcontrib><creatorcontrib>Inigo, Joseph R.</creatorcontrib><creatorcontrib>Kumar, Rahul</creatorcontrib><creatorcontrib>Chaudhary, Ajay K.</creatorcontrib><creatorcontrib>O'Malley, Jordan</creatorcontrib><creatorcontrib>Balachandar, Srimmitha</creatorcontrib><creatorcontrib>Wang, Jianmin</creatorcontrib><creatorcontrib>Attwood, Kristopher</creatorcontrib><creatorcontrib>Yadav, Neelu</creatorcontrib><creatorcontrib>Hochwald, Steven</creatorcontrib><creatorcontrib>Wang, Xinjiang</creatorcontrib><creatorcontrib>Chandra, Dhyan</creatorcontrib><title>Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Pancreatic ductal adenocarcinoma (PDAC) is highly aggressive disease and current treatment regimens fail to effectively cure PDAC. Development of resistance to current therapy is one of the key reasons for this outcome. Nimbolide (NL), a triterpenoid obtained from Azadirachta indica, exhibits anticancer properties in various cancer including PDAC cells. However, the underlying mechanism of this anticancer agent in PDAC cells remains undefined. We show that NL exerts a higher level of apoptotic cell death compared to the first-line agent gemcitabine for PDAC, as well as other anticancer agents including sorafenib and curcumin. The anticancer efficacy of NL was further evidenced by a reduction in the CD44+ as well as cancer stem-like cell (CSC) population, as it causes decreased sphere formation. Mechanistically, the anticancer efficacy of NL associates with reduced mutant p53 as well as increased mitochondrial activity in the form of increased mitochondrial reactive oxygen species and mitochondrial mass. Together, this study highlights the therapeutic potential of NL in mutant p53 expressing pancreatic cancer.
•Nimbolide is a more effective caspase activator compared to gemcitabine.•Nimbolide treatment depletes CD44+ population in pancreatic cancer cells.•Nimbolide-induced apoptosis associates with increased mitochondrial activity.•Reduced levels of mutant p53 may contribute to anticancer effects of nimbolide.</description><subject>Adenocarcinoma</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Antitumor agents</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Cancer stem cells</subject><subject>Cancer therapies</subject><subject>Carcinoma, Pancreatic Ductal - drug therapy</subject><subject>Carcinoma, Pancreatic Ductal - genetics</subject><subject>Carcinoma, Pancreatic Ductal - metabolism</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>Caspase Inhibitors - pharmacology</subject><subject>CD44 antigen</subject><subject>Cell death</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - drug effects</subject><subject>Cells</subject><subject>Chemotherapy</subject><subject>Curcumin</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Deoxycytidine - pharmacology</subject><subject>Disease</subject><subject>Dose-Response Relationship, Drug</subject><subject>Gemcitabine</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Immunoglobulins</subject><subject>Kinases</subject><subject>Life sciences</subject><subject>Limonins - pharmacology</subject><subject>Medical treatment</subject><subject>Metastasis</subject><subject>Mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondria - pathology</subject><subject>Mutant p53</subject><subject>Mutation</subject><subject>Neoplastic Stem Cells - drug effects</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Nimbolide</subject><subject>p53 Protein</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Penicillin</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Thyroid cancer</subject><subject>Time Factors</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9UU2PFCEQJUbjzq7-A2NIPPdYdEPTXEzMrLomG73omdBQ7TLpgRboSfz3Ms666sUTod5HvdQj5AWDLQPWv95vrQkzlm0LTNbRFlr1iGzYINtGqgEekw10wJtu6MQFucx5DwCCS_GUXLSKgWQMNiR88ocxzt4hTehWi5nurjmnS8y--CNSi_Ncf8s6m-JjoCY46sOZefAl2rsYXPJmpqaySpXlitPFBJuwSiytMS2mX0b5GXkymTnj8_v3inx9_-7L7qa5_fzh4-7tbWO5YqVxbhz7wfGBd85wgVZKIwClUU7BOIgKM2tb1k2WSTU5OU6m50xw0ULfg-2uyJuz77KOB3QWQ0lm1kvyB5N-6Gi8_hcJ_k5_i0ctJPSiZ9Xg1b1Bit9XzEXv45pCzayZ6pUauBKisviZZVPMOeH0sIGBPrWk9_rckj61dJrWlqrs5d_pHkS_a_kTH-uNjh6TztZjPaPzCW3RLvr_b_gJ8w6oYw</recordid><startdate>20180128</startdate><enddate>20180128</enddate><creator>Kumar, Sandeep</creator><creator>Inigo, Joseph R.</creator><creator>Kumar, Rahul</creator><creator>Chaudhary, Ajay K.</creator><creator>O'Malley, Jordan</creator><creator>Balachandar, Srimmitha</creator><creator>Wang, Jianmin</creator><creator>Attwood, Kristopher</creator><creator>Yadav, Neelu</creator><creator>Hochwald, Steven</creator><creator>Wang, Xinjiang</creator><creator>Chandra, Dhyan</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7272-9384</orcidid></search><sort><creationdate>20180128</creationdate><title>Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells</title><author>Kumar, Sandeep ; Inigo, Joseph R. ; Kumar, Rahul ; Chaudhary, Ajay K. ; O'Malley, Jordan ; Balachandar, Srimmitha ; Wang, Jianmin ; Attwood, Kristopher ; Yadav, Neelu ; Hochwald, Steven ; Wang, Xinjiang ; Chandra, Dhyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenocarcinoma</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Antitumor agents</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Cancer stem cells</topic><topic>Cancer therapies</topic><topic>Carcinoma, Pancreatic Ductal - drug therapy</topic><topic>Carcinoma, Pancreatic Ductal - genetics</topic><topic>Carcinoma, Pancreatic Ductal - metabolism</topic><topic>Carcinoma, Pancreatic Ductal - pathology</topic><topic>Caspase Inhibitors - pharmacology</topic><topic>CD44 antigen</topic><topic>Cell death</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - drug effects</topic><topic>Cells</topic><topic>Chemotherapy</topic><topic>Curcumin</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Deoxycytidine - pharmacology</topic><topic>Disease</topic><topic>Dose-Response Relationship, Drug</topic><topic>Gemcitabine</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Immunoglobulins</topic><topic>Kinases</topic><topic>Life sciences</topic><topic>Limonins - pharmacology</topic><topic>Medical treatment</topic><topic>Metastasis</topic><topic>Mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondria - pathology</topic><topic>Mutant p53</topic><topic>Mutation</topic><topic>Neoplastic Stem Cells - drug effects</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Neoplastic Stem Cells - pathology</topic><topic>Nimbolide</topic><topic>p53 Protein</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Penicillin</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Thyroid cancer</topic><topic>Time Factors</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Sandeep</creatorcontrib><creatorcontrib>Inigo, Joseph R.</creatorcontrib><creatorcontrib>Kumar, Rahul</creatorcontrib><creatorcontrib>Chaudhary, Ajay K.</creatorcontrib><creatorcontrib>O'Malley, Jordan</creatorcontrib><creatorcontrib>Balachandar, Srimmitha</creatorcontrib><creatorcontrib>Wang, Jianmin</creatorcontrib><creatorcontrib>Attwood, Kristopher</creatorcontrib><creatorcontrib>Yadav, Neelu</creatorcontrib><creatorcontrib>Hochwald, Steven</creatorcontrib><creatorcontrib>Wang, Xinjiang</creatorcontrib><creatorcontrib>Chandra, Dhyan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Sandeep</au><au>Inigo, Joseph R.</au><au>Kumar, Rahul</au><au>Chaudhary, Ajay K.</au><au>O'Malley, Jordan</au><au>Balachandar, Srimmitha</au><au>Wang, Jianmin</au><au>Attwood, Kristopher</au><au>Yadav, Neelu</au><au>Hochwald, Steven</au><au>Wang, Xinjiang</au><au>Chandra, Dhyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2018-01-28</date><risdate>2018</risdate><volume>413</volume><spage>82</spage><epage>93</epage><pages>82-93</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>Pancreatic ductal adenocarcinoma (PDAC) is highly aggressive disease and current treatment regimens fail to effectively cure PDAC. Development of resistance to current therapy is one of the key reasons for this outcome. Nimbolide (NL), a triterpenoid obtained from Azadirachta indica, exhibits anticancer properties in various cancer including PDAC cells. However, the underlying mechanism of this anticancer agent in PDAC cells remains undefined. We show that NL exerts a higher level of apoptotic cell death compared to the first-line agent gemcitabine for PDAC, as well as other anticancer agents including sorafenib and curcumin. The anticancer efficacy of NL was further evidenced by a reduction in the CD44+ as well as cancer stem-like cell (CSC) population, as it causes decreased sphere formation. Mechanistically, the anticancer efficacy of NL associates with reduced mutant p53 as well as increased mitochondrial activity in the form of increased mitochondrial reactive oxygen species and mitochondrial mass. Together, this study highlights the therapeutic potential of NL in mutant p53 expressing pancreatic cancer.
•Nimbolide is a more effective caspase activator compared to gemcitabine.•Nimbolide treatment depletes CD44+ population in pancreatic cancer cells.•Nimbolide-induced apoptosis associates with increased mitochondrial activity.•Reduced levels of mutant p53 may contribute to anticancer effects of nimbolide.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>29107110</pmid><doi>10.1016/j.canlet.2017.10.029</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7272-9384</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Antineoplastic Agents, Phytogenic - pharmacology Antitumor agents Apoptosis Apoptosis - drug effects Cancer stem cells Cancer therapies Carcinoma, Pancreatic Ductal - drug therapy Carcinoma, Pancreatic Ductal - genetics Carcinoma, Pancreatic Ductal - metabolism Carcinoma, Pancreatic Ductal - pathology Caspase Inhibitors - pharmacology CD44 antigen Cell death Cell Line, Tumor Cell Movement - drug effects Cells Chemotherapy Curcumin Deoxycytidine - analogs & derivatives Deoxycytidine - pharmacology Disease Dose-Response Relationship, Drug Gemcitabine Growth factors Humans Hyaluronan Receptors - metabolism Immunoglobulins Kinases Life sciences Limonins - pharmacology Medical treatment Metastasis Mitochondria Mitochondria - drug effects Mitochondria - metabolism Mitochondria - pathology Mutant p53 Mutation Neoplastic Stem Cells - drug effects Neoplastic Stem Cells - metabolism Neoplastic Stem Cells - pathology Nimbolide p53 Protein Pancreatic cancer Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - genetics Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology Penicillin Reactive oxygen species Reactive Oxygen Species - metabolism Thyroid cancer Time Factors Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism |
title | Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells |
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