Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Cancer letters 2018-01, Vol.413, p.82-93
Main Authors: 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
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3
cites cdi_FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3
container_end_page 93
container_issue
container_start_page 82
container_title Cancer letters
container_volume 413
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
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5706561</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0304383517306663</els_id><sourcerecordid>1969984955</sourcerecordid><originalsourceid>FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3</originalsourceid><addsrcrecordid>eNp9UU2PFCEQJUbjzq7-A2NIPPdYdEPTXEzMrLomG73omdBQ7TLpgRboSfz3Ms666sUTod5HvdQj5AWDLQPWv95vrQkzlm0LTNbRFlr1iGzYINtGqgEekw10wJtu6MQFucx5DwCCS_GUXLSKgWQMNiR88ocxzt4hTehWi5nurjmnS8y--CNSi_Ncf8s6m-JjoCY46sOZefAl2rsYXPJmpqaySpXlitPFBJuwSiytMS2mX0b5GXkymTnj8_v3inx9_-7L7qa5_fzh4-7tbWO5YqVxbhz7wfGBd85wgVZKIwClUU7BOIgKM2tb1k2WSTU5OU6m50xw0ULfg-2uyJuz77KOB3QWQ0lm1kvyB5N-6Gi8_hcJ_k5_i0ctJPSiZ9Xg1b1Bit9XzEXv45pCzayZ6pUauBKisviZZVPMOeH0sIGBPrWk9_rckj61dJrWlqrs5d_pHkS_a_kTH-uNjh6TztZjPaPzCW3RLvr_b_gJ8w6oYw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1969984955</pqid></control><display><type>article</type><title>Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells</title><source>Elsevier</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 &amp; 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 &amp; 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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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>
fulltext fulltext
identifier ISSN: 0304-3835
ispartof Cancer letters, 2018-01, Vol.413, p.82-93
issn 0304-3835
1872-7980
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5706561
source Elsevier
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T17%3A53%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nimbolide%20reduces%20CD44%20positive%20cell%20population%20and%20induces%20mitochondrial%20apoptosis%20in%20pancreatic%20cancer%20cells&rft.jtitle=Cancer%20letters&rft.au=Kumar,%20Sandeep&rft.date=2018-01-28&rft.volume=413&rft.spage=82&rft.epage=93&rft.pages=82-93&rft.issn=0304-3835&rft.eissn=1872-7980&rft_id=info:doi/10.1016/j.canlet.2017.10.029&rft_dat=%3Cproquest_pubme%3E1969984955%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c491t-ddbb68d4843da45ec77a50e7a9d90b85dbb1cc213fc179fd7bfa64154520660c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1969984955&rft_id=info:pmid/29107110&rfr_iscdi=true