Epithelial Cell Adhesion Molecule (EpCAM) Expression Can Be Modulated via NFκB

The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, i...

Full description

Saved in:
Bibliographic Details
Published inBiomedicines Vol. 10; no. 11; p. 2985
Main Authors Zia, Saadiya, Tehreem, Komal, Batool, Sidra, Ishfaq, Mehreen, Mirza, Shaher Bano, Khan, Shahrukh, Almashjary, Majed N., Hazzazi, Mohannad S., Qanash, Husam, Shaikh, Ahmad, Baty, Roua S., Jafri, Ibrahim, Alsubhi, Nouf H., Alrefaei, Ghadeer I., Sami, Rokayya, Shahid, Ramla
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 20.11.2022
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, is a medicinal herb with anticancer properties. Expression of EpCAM and its downstream target genes (Myc and TERT) wasdownregulated upon treatment with costunolide in Jurkat cells. A significant change in the telomere length of Jurkat cells was not noted at 72 h of costunolide treatment. An in silico study revealed hydrophobic interactions between EpCAM extracellular domain and Myc bHLH with costunolide. Reduced expression of NFκB, a transcription factor of EpCAM, Myc, and TERT in costunolide-treated Jurkat cells, suggested that costunolide inhibits gene expression by targeting NFκB and its downstream targets. Overall, the study proposes that costunolide could be a promising therapeutic biomolecule for leukemia.
AbstractList The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, is a medicinal herb with anticancer properties. Expression of and its downstream target genes ( and ) wasdownregulated upon treatment with costunolide in Jurkat cells. A significant change in the telomere length of Jurkat cells was not noted at 72 h of costunolide treatment. An in silico study revealed hydrophobic interactions between EpCAM extracellular domain and Myc bHLH with costunolide. Reduced expression of , a transcription factor of , and in costunolide-treated Jurkat cells, suggested that costunolide inhibits gene expression by targeting NFκB and its downstream targets. Overall, the study proposes that costunolide could be a promising therapeutic biomolecule for leukemia.
The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, is a medicinal herb with anticancer properties. Expression of EpCAM and its downstream target genes (Myc and TERT) wasdownregulated upon treatment with costunolide in Jurkat cells. A significant change in the telomere length of Jurkat cells was not noted at 72 h of costunolide treatment. An in silico study revealed hydrophobic interactions between EpCAM extracellular domain and Myc bHLH with costunolide. Reduced expression of NFκB, a transcription factor of EpCAM, Myc, and TERT in costunolide-treated Jurkat cells, suggested that costunolide inhibits gene expression by targeting NFκB and its downstream targets. Overall, the study proposes that costunolide could be a promising therapeutic biomolecule for leukemia.
The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, is a medicinal herb with anticancer properties. Expression of EpCAM and its downstream target genes (Myc and TERT) wasdownregulated upon treatment with costunolide in Jurkat cells. A significant change in the telomere length of Jurkat cells was not noted at 72 h of costunolide treatment. An in silico study revealed hydrophobic interactions between EpCAM extracellular domain and Myc bHLH with costunolide. Reduced expression of NFκB, a transcription factor of EpCAM, Myc, and TERT in costunolide-treated Jurkat cells, suggested that costunolide inhibits gene expression by targeting NFκB and its downstream targets. Overall, the study proposes that costunolide could be a promising therapeutic biomolecule for leukemia.The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, is a medicinal herb with anticancer properties. Expression of EpCAM and its downstream target genes (Myc and TERT) wasdownregulated upon treatment with costunolide in Jurkat cells. A significant change in the telomere length of Jurkat cells was not noted at 72 h of costunolide treatment. An in silico study revealed hydrophobic interactions between EpCAM extracellular domain and Myc bHLH with costunolide. Reduced expression of NFκB, a transcription factor of EpCAM, Myc, and TERT in costunolide-treated Jurkat cells, suggested that costunolide inhibits gene expression by targeting NFκB and its downstream targets. Overall, the study proposes that costunolide could be a promising therapeutic biomolecule for leukemia.
The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases. Costunolide, a sesquiterpene lactone found in crepe ginger and lettuce, is a medicinal herb with anticancer properties. Expression of EpCAM and its downstream target genes ( Myc and TERT ) wasdownregulated upon treatment with costunolide in Jurkat cells. A significant change in the telomere length of Jurkat cells was not noted at 72 h of costunolide treatment. An in silico study revealed hydrophobic interactions between EpCAM extracellular domain and Myc bHLH with costunolide. Reduced expression of NFκB , a transcription factor of EpCAM , Myc, and TERT in costunolide-treated Jurkat cells, suggested that costunolide inhibits gene expression by targeting NFκB and its downstream targets. Overall, the study proposes that costunolide could be a promising therapeutic biomolecule for leukemia.
Author Shahid, Ramla
Baty, Roua S.
Hazzazi, Mohannad S.
Khan, Shahrukh
Shaikh, Ahmad
Alrefaei, Ghadeer I.
Zia, Saadiya
Jafri, Ibrahim
Alsubhi, Nouf H.
Qanash, Husam
Tehreem, Komal
Ishfaq, Mehreen
Batool, Sidra
Mirza, Shaher Bano
Sami, Rokayya
Almashjary, Majed N.
AuthorAffiliation 1 Department of Biosciences, COMSATS University Islamabad (CUI), Islamabad 45550, Pakistan
4 Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdul Aziz University, Jeddah 22254, Saudi Arabia
8 Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, P.O. Box 960, Abha 61421, Saudi Arabia
2 Department of Biochemistry, Faculty of Sciences, University of Agriculture Faisalabad, Faisalabad 38000, Pakistan
10 Biological Sciences Department, College of Science and Arts, King Abdul Aziz University, Rabigh 21911, Saudi Arabia
6 Department of Medical Laboratory Science, College of Applied Medical Sciences, University of Ha’il, Hail 55476, Saudi Arabia
5 Hematology Research Unit, King Fahd Medical Research Center, King Abdul Aziz University, Jeddah 22254, Saudi Arabia
9 Department of Biotechnology, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia
3 Research School of Chemistry, Australian Na
AuthorAffiliation_xml – name: 1 Department of Biosciences, COMSATS University Islamabad (CUI), Islamabad 45550, Pakistan
– name: 5 Hematology Research Unit, King Fahd Medical Research Center, King Abdul Aziz University, Jeddah 22254, Saudi Arabia
– name: 10 Biological Sciences Department, College of Science and Arts, King Abdul Aziz University, Rabigh 21911, Saudi Arabia
– name: 4 Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdul Aziz University, Jeddah 22254, Saudi Arabia
– name: 9 Department of Biotechnology, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia
– name: 6 Department of Medical Laboratory Science, College of Applied Medical Sciences, University of Ha’il, Hail 55476, Saudi Arabia
– name: 8 Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, P.O. Box 960, Abha 61421, Saudi Arabia
– name: 2 Department of Biochemistry, Faculty of Sciences, University of Agriculture Faisalabad, Faisalabad 38000, Pakistan
– name: 7 Molecular Diagnostics and Personalized Therapeutics Unit, University of Ha’il, Hail 55476, Saudi Arabia
– name: 11 Department of Biology, College of Science, University of Jeddah, P.O. Box 80327, Jeddah 21589, Saudi Arabia
– name: 3 Research School of Chemistry, Australian National University, Canberra, ACT 2600, Australia
– name: 12 Department of Food Science and Nutrition, College of Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia
Author_xml – sequence: 1
  givenname: Saadiya
  orcidid: 0000-0002-2265-0667
  surname: Zia
  fullname: Zia, Saadiya
– sequence: 2
  givenname: Komal
  surname: Tehreem
  fullname: Tehreem, Komal
– sequence: 3
  givenname: Sidra
  surname: Batool
  fullname: Batool, Sidra
– sequence: 4
  givenname: Mehreen
  surname: Ishfaq
  fullname: Ishfaq, Mehreen
– sequence: 5
  givenname: Shaher Bano
  surname: Mirza
  fullname: Mirza, Shaher Bano
– sequence: 6
  givenname: Shahrukh
  orcidid: 0000-0002-8536-3585
  surname: Khan
  fullname: Khan, Shahrukh
– sequence: 7
  givenname: Majed N.
  orcidid: 0000-0002-6619-0287
  surname: Almashjary
  fullname: Almashjary, Majed N.
– sequence: 8
  givenname: Mohannad S.
  orcidid: 0000-0002-6321-8248
  surname: Hazzazi
  fullname: Hazzazi, Mohannad S.
– sequence: 9
  givenname: Husam
  orcidid: 0000-0002-3068-0313
  surname: Qanash
  fullname: Qanash, Husam
– sequence: 10
  givenname: Ahmad
  orcidid: 0000-0002-7001-4200
  surname: Shaikh
  fullname: Shaikh, Ahmad
– sequence: 11
  givenname: Roua S.
  orcidid: 0000-0001-5324-0014
  surname: Baty
  fullname: Baty, Roua S.
– sequence: 12
  givenname: Ibrahim
  orcidid: 0000-0002-8465-6829
  surname: Jafri
  fullname: Jafri, Ibrahim
– sequence: 13
  givenname: Nouf H.
  orcidid: 0000-0003-4450-0210
  surname: Alsubhi
  fullname: Alsubhi, Nouf H.
– sequence: 14
  givenname: Ghadeer I.
  orcidid: 0000-0003-0615-5321
  surname: Alrefaei
  fullname: Alrefaei, Ghadeer I.
– sequence: 15
  givenname: Rokayya
  orcidid: 0000-0003-3162-9453
  surname: Sami
  fullname: Sami, Rokayya
– sequence: 16
  givenname: Ramla
  orcidid: 0000-0001-7707-6431
  surname: Shahid
  fullname: Shahid, Ramla
BackLink https://www.ncbi.nlm.nih.gov/pubmed/36428553$$D View this record in MEDLINE/PubMed
BookMark eNp9kt1OFDEUgCcGI4i8gTGTeAMXq_2dtl6QLJtFSUBu9LrptKdsN93pOJ0h-mo8hM9kYcEAMfamTc93vp6c09fVTpc6qKq3GH2gVKGPbUgbcMGGDjJGGBMl-YtqjxAiZgpxtfPovFsd5LxGZSlMJWavql3aMCI5p3vV5bIP4wpiMLFeQIz13K0gh9TVFymCnSLUh8t-Mb84qpc_-wHyXWxhuvoECuKmaEZw9XUw9dfT3zcnb6qX3sQMB_f7fvX9dPlt8WV2fvn5bDE_n1lGyTizUvqGSgSCK2kcVo57ZLxvmfXENK3lYAUgaijhDINTrmXCOqscZV60hO5XZ1uvS2at-yFszPBLJxP03UUarrQZxmAjaI6sE5IBNh4xiplURiouWu-sNV6g4jreuvqpLV210I2DiU-kTyNdWOmrdK1VI0WjaBEc3guG9GOCPOpNyLZ003SQpqyJYIiXtwkv6Ptn6DpNQ1dadUtJIhCXolDvHlf0t5SHuRXg0xawQ8p5AK9tGM1YZlMKDFFjpG__if7XPynJ7Fnyg_-_aX8AfArFZg
CitedBy_id crossref_primary_10_1166_mex_2023_2569
crossref_primary_10_1166_sam_2024_4604
crossref_primary_10_3390_biomedicines12030471
Cites_doi 10.1038/bjc.2011.231
10.1016/j.biopha.2019.109659
10.1016/j.bbamem.2013.04.018
10.1038/bjc.2014.366
10.3390/cells9061361
10.3390/ijms20122926
10.1158/0008-5472.CAN-16-0842
10.1016/j.bbcan.2020.188436
10.1002/ptr.5155
10.1074/jbc.M116.748129
10.1007/BF02976606
10.1186/s13765-020-00514-0
10.1093/nar/gku1111
10.1021/acs.molpharmaceut.9b00185
10.2147/DDDT.S264077
10.3389/fimmu.2020.589929
10.1016/j.critrevonc.2018.03.006
10.15698/cst2019.06.188
10.1371/journal.pone.0189558
10.1155/2013/936257
10.1038/bjc.2013.536
10.1016/j.biopha.2020.109955
10.1073/pnas.1913242117
10.1016/j.gene.2018.08.048
10.1002/cam4.1218
10.18632/oncotarget.5380
10.1097/MD.0000000000023342
10.1186/1476-4598-12-56
10.1016/j.jphs.2015.01.002
10.1248/bpb.31.1024
10.18632/oncotarget.1643
10.1021/acsomega.0c02113
10.1074/jbc.M007378200
10.1016/j.semcancer.2015.02.006
10.1021/jm049937r
10.1111/his.12870
10.3389/fphar.2018.01469
10.1093/nar/30.10.e47
10.1098/rspb.2014.1610
10.3892/ol.2014.2140
10.1038/ncomms5764
10.3390/ijms22042075
10.1016/j.biopha.2016.03.031
ContentType Journal Article
Copyright 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2022 by the authors. 2022
Copyright_xml – notice: 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2022 by the authors. 2022
DBID AAYXX
CITATION
NPM
8FE
8FH
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
GNUQQ
HCIFZ
LK8
M7P
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.3390/biomedicines10112985
DatabaseName CrossRef
PubMed
ProQuest SciTech Collection
ProQuest Natural Science Collection
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central
ProQuest Central Student
SciTech Premium Collection
ProQuest Biological Science Collection
Biological Science Database
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Biological Science Collection
ProQuest Central Essentials
ProQuest One Academic Eastern Edition
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest Natural Science Collection
Biological Science Database
ProQuest SciTech Collection
ProQuest Central China
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest One Academic UKI Edition
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
ProQuest Central (New)
ProQuest One Academic
ProQuest One Academic (New)
MEDLINE - Academic
DatabaseTitleList PubMed
CrossRef

Publicly Available Content Database
MEDLINE - Academic

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Engineering
EISSN 2227-9059
ExternalDocumentID oai_doaj_org_article_50cd784e1af0431489a8957bfdccaf70
PMC9687693
36428553
10_3390_biomedicines10112985
Genre Journal Article
GeographicLocations United States--US
GeographicLocations_xml – name: United States--US
GroupedDBID 53G
5VS
8FE
8FH
AADQD
AAFWJ
AAYXX
ACPRK
ADBBV
AFKRA
AFPKN
AFZYC
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BBNVY
BCNDV
BENPR
BHPHI
CCPQU
CITATION
EMOBN
GROUPED_DOAJ
GX1
HCIFZ
HYE
IAO
IHR
INH
ITC
KQ8
LK8
M7P
MODMG
M~E
OK1
PGMZT
PHGZM
PHGZT
PIMPY
PROAC
RPM
NPM
ABUWG
AZQEC
DWQXO
GNUQQ
PKEHL
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c432t-c88f6380e7598ad19d5f0affb4cf2a6bc5ec7e03a32541ed9db47cdc9d34f7b23
IEDL.DBID BENPR
ISSN 2227-9059
IngestDate Wed Aug 27 01:30:32 EDT 2025
Thu Aug 21 18:39:20 EDT 2025
Fri Jul 11 15:35:16 EDT 2025
Fri Jul 25 12:01:49 EDT 2025
Thu Jan 02 22:53:42 EST 2025
Thu Apr 24 22:56:10 EDT 2025
Tue Jul 01 03:17:25 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 11
Keywords costunolide
cell proliferation
acute lymphoblastic leukemia
telomerase inhibition
epithelial cell adhesion molecule
Language English
License https://creativecommons.org/licenses/by/4.0
Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c432t-c88f6380e7598ad19d5f0affb4cf2a6bc5ec7e03a32541ed9db47cdc9d34f7b23
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-7707-6431
0000-0001-5324-0014
0000-0002-6321-8248
0000-0002-6619-0287
0000-0003-3162-9453
0000-0002-8465-6829
0000-0002-7001-4200
0000-0003-4450-0210
0000-0002-2265-0667
0000-0002-8536-3585
0000-0003-0615-5321
0000-0002-3068-0313
OpenAccessLink https://www.proquest.com/docview/2748270587?pq-origsite=%requestingapplication%
PMID 36428553
PQID 2748270587
PQPubID 2032426
ParticipantIDs doaj_primary_oai_doaj_org_article_50cd784e1af0431489a8957bfdccaf70
pubmedcentral_primary_oai_pubmedcentral_nih_gov_9687693
proquest_miscellaneous_2740504325
proquest_journals_2748270587
pubmed_primary_36428553
crossref_citationtrail_10_3390_biomedicines10112985
crossref_primary_10_3390_biomedicines10112985
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20221120
PublicationDateYYYYMMDD 2022-11-20
PublicationDate_xml – month: 11
  year: 2022
  text: 20221120
  day: 20
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
– name: Basel
PublicationTitle Biomedicines
PublicationTitleAlternate Biomedicines
PublicationYear 2022
Publisher MDPI AG
MDPI
Publisher_xml – name: MDPI AG
– name: MDPI
References Cawthon (ref_25) 2002; 30
Huang (ref_40) 2017; 7
Keller (ref_33) 2019; 3
ref_12
Mal (ref_9) 2020; 5
Dratwa (ref_10) 2020; 11
Zhdanov (ref_41) 2017; 6
Pierce (ref_47) 1994; 14
ref_51
Kazemier (ref_50) 2011; 105
Huang (ref_48) 2014; 5
Peng (ref_14) 2017; 7
ref_16
Yao (ref_45) 2020; 14
Ma (ref_42) 2019; 16
Bell (ref_1) 2020; 117
Tabata (ref_13) 2015; 127
Choi (ref_17) 2013; 2013
Schnell (ref_5) 2013; 1828
Huang (ref_22) 2021; 11
Yin (ref_46) 2000; 275
Ramesh (ref_15) 2021; 36
Choi (ref_37) 2002; 25
Zhang (ref_6) 2017; 39
Siedle (ref_20) 2004; 47
Jin (ref_23) 2020; 121
Mao (ref_53) 2018; 9
Nettle (ref_26) 2015; 282
Fagotto (ref_3) 2020; 1874
Massoner (ref_2) 2014; 111
Sen (ref_35) 2016; 68
(ref_27) 2014; 5
Vallera (ref_32) 2013; 28
Wang (ref_18) 2017; 7
Pitchai (ref_54) 2014; 28
Nan (ref_52) 2020; 63
Zheng (ref_7) 2017; 77
Ren (ref_44) 2020; 99
Kanno (ref_38) 2008; 31
Zhang (ref_24) 2016; 80
Mu (ref_34) 2014; 8
Jakobs (ref_19) 2016; 291
Dreos (ref_29) 2015; 43
Feitelson (ref_30) 2015; 35
Martowicz (ref_4) 2013; 12
Hekimian (ref_36) 2012; 2012
ref_43
Warneke (ref_31) 2013; 109
Sirera (ref_49) 2018; 126
Zhao (ref_28) 2015; 6
ref_8
Zach (ref_39) 2019; 2
Hu (ref_21) 2018; 678
Li (ref_11) 2020; 125
References_xml – volume: 105
  start-page: 312
  year: 2011
  ident: ref_50
  article-title: Transcription factors and molecular epigenetic marks underlying EpCAM overexpression in ovarian cancer
  publication-title: Br. J. Cancer
  doi: 10.1038/bjc.2011.231
– volume: 121
  start-page: 109659
  year: 2020
  ident: ref_23
  article-title: Costunolide inhibits osteosarcoma growth and metastasis via suppressing STAT3 signal pathway
  publication-title: Biomed. Pharmacother.
  doi: 10.1016/j.biopha.2019.109659
– volume: 2
  start-page: 334
  year: 2019
  ident: ref_39
  article-title: The effects of Rapamycin on Telomerase Activity and Regulation in Cancer Cells
  publication-title: Br. J. Cancer Res.
– ident: ref_51
– volume: 1828
  start-page: 1989
  year: 2013
  ident: ref_5
  article-title: EpCAM: Structure and function in health and disease
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/j.bbamem.2013.04.018
– volume: 111
  start-page: 955
  year: 2014
  ident: ref_2
  article-title: EpCAM is overexpressed in local and metastatic prostate cancer, suppressed by chemotherapy and modulated by MET-associated miRNA-200c/205
  publication-title: Br. J. Cancer
  doi: 10.1038/bjc.2014.366
– ident: ref_8
  doi: 10.3390/cells9061361
– ident: ref_12
  doi: 10.3390/ijms20122926
– volume: 77
  start-page: 482
  year: 2017
  ident: ref_7
  article-title: EpCAM inhibition sensitizes chemoresistant leukemia to immune surveillance
  publication-title: Cancer Res.
  doi: 10.1158/0008-5472.CAN-16-0842
– volume: 1874
  start-page: 188436
  year: 2020
  ident: ref_3
  article-title: EpCAM cellular functions in adhesion and migration, and potential impact on invasion: A critical review
  publication-title: Biochim. Et Biophys. Acta (BBA)-Rev. Cancer
  doi: 10.1016/j.bbcan.2020.188436
– volume: 7
  start-page: 1270
  year: 2017
  ident: ref_18
  article-title: Dehydrocostus lactone, a natural sesquiterpene lactone, suppresses the biological characteristics of glioma, through inhibition of the NF-κB/COX-2 signaling pathway by targeting IKKβ
  publication-title: Am. J. Cancer Res.
– volume: 28
  start-page: 1499
  year: 2014
  ident: ref_54
  article-title: In Vitro and In Silico Evaluation of NF-κB Targeted Costunolide Action on Estrogen Receptor-Negative Breast Cancer Cells—A Comparison with Normal Breast Cells
  publication-title: Phytother. Res.
  doi: 10.1002/ptr.5155
– volume: 291
  start-page: 26098
  year: 2016
  ident: ref_19
  article-title: Helenalin acetate, a natural sesquiterpene lactone with anti-inflammatory and anti-cancer activity, disrupts the cooperation of CCAAT box/enhancer-binding protein β (C/EBPβ) and co-activator p300
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M116.748129
– volume: 25
  start-page: 480
  year: 2002
  ident: ref_37
  article-title: Costunolide induces differentiation of human leukemia HL-60 cells
  publication-title: Arch. Pharmacal Res.
  doi: 10.1007/BF02976606
– volume: 63
  start-page: 1
  year: 2020
  ident: ref_52
  article-title: Costunolide inhibits inflammation in LPS-induced RAW264. 7 cells and ameliorates gastric acid reflux-induced esophageal injury in rat model
  publication-title: Appl. Biol. Chem.
  doi: 10.1186/s13765-020-00514-0
– volume: 43
  start-page: D92
  year: 2015
  ident: ref_29
  article-title: The Eukaryotic Promoter Database: Expansion of EPDnew and new promoter analysis tools
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/gku1111
– volume: 16
  start-page: 2199
  year: 2019
  ident: ref_42
  article-title: Identification of tumor specific peptide as EpCAM ligand and its potential diagnostic and therapeutic clinical application
  publication-title: Mol. Pharm.
  doi: 10.1021/acs.molpharmaceut.9b00185
– volume: 14
  start-page: 3983
  year: 2020
  ident: ref_45
  article-title: Identification of a novel c-Myc inhibitor 7594-0037 by structure-based virtual screening and investigation of its anti-cancer effect on multiple myeloma
  publication-title: Drug Des. Dev. Ther.
  doi: 10.2147/DDDT.S264077
– volume: 11
  start-page: 589929
  year: 2020
  ident: ref_10
  article-title: TERT—Regulation and Roles in Cancer Formation
  publication-title: Front. Immunol.
  doi: 10.3389/fimmu.2020.589929
– volume: 126
  start-page: 52
  year: 2018
  ident: ref_49
  article-title: EpCAM duality becomes this molecule in a new Dr. Jekyll and Mr. Hyde tale
  publication-title: Crit. Rev. Oncol. Hematol.
  doi: 10.1016/j.critrevonc.2018.03.006
– volume: 39
  start-page: 1
  year: 2017
  ident: ref_6
  article-title: The role of epithelial cell adhesion molecule N-glycosylation on apoptosis in breast cancer cells
  publication-title: Tumor Biol.
– volume: 28
  start-page: 274
  year: 2013
  ident: ref_32
  article-title: Heterodimeric bispecific single-chain variable-fragment antibodies against EpCAM and CD16 induce effective antibody-dependent cellular cytotoxicity against human carcinoma cells
  publication-title: Cancer Biother. Radiopharm.
– volume: 3
  start-page: 165
  year: 2019
  ident: ref_33
  article-title: Biology and clinical relevance of EpCAM
  publication-title: Cell Stress.
  doi: 10.15698/cst2019.06.188
– ident: ref_43
  doi: 10.1371/journal.pone.0189558
– volume: 2013
  start-page: 936257
  year: 2013
  ident: ref_17
  article-title: Saussurealappa Clarke-derived costunolide prevents TNFα-induced breast cancer cell migration and invasion by inhibiting NF-κB activity
  publication-title: Evid.-Based Complement. Altern. Med.
  doi: 10.1155/2013/936257
– volume: 109
  start-page: 2217
  year: 2013
  ident: ref_31
  article-title: Members of the EpCAMsignalling pathway are expressed in gastric cancer tissue and are correlated with patient prognosis
  publication-title: Br. J. Cancer
  doi: 10.1038/bjc.2013.536
– volume: 125
  start-page: 109955
  year: 2020
  ident: ref_11
  article-title: Antitumor activity and mechanism of costunolide and dehydrocostus lactone: Two natural sesquiterpene lactones from the Asteraceae family
  publication-title: Biomed. Pharm.
  doi: 10.1016/j.biopha.2020.109955
– volume: 117
  start-page: 8486
  year: 2020
  ident: ref_1
  article-title: In silico design and validation of high-affinity RNA aptamers targeting epithelial cellular adhesion molecule dimers
  publication-title: Proc. Natl. Acad. Sci. USA
  doi: 10.1073/pnas.1913242117
– volume: 2012
  start-page: 601810
  year: 2012
  ident: ref_36
  article-title: Epithelial cell dissemination and readhesion: Analysis of factors contributing to metastasis formation in breast cancer
  publication-title: Int. Sch. Res. Not.
– volume: 678
  start-page: 261
  year: 2018
  ident: ref_21
  article-title: Activation of p53 by costunolide blocks glutaminolysis and inhibits proliferation in human colorectal cancer cells
  publication-title: Gene
  doi: 10.1016/j.gene.2018.08.048
– volume: 6
  start-page: 2697
  year: 2017
  ident: ref_41
  article-title: Inhibition of telomerase activity and induction of apoptosis by Rhodospirillum rubrum l-asparaginase in cancer Jurkat cell line and normal human CD4+ T lymphocytes
  publication-title: Cancer Med.
  doi: 10.1002/cam4.1218
– volume: 6
  start-page: 38934
  year: 2015
  ident: ref_28
  article-title: Inhibition of MYC with involvement of ERK/JNK/MAPK and AKT pathways as a novel mechanism for shikonin and its derivatives in killing leukemia cells
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.5380
– volume: 99
  start-page: e23342
  year: 2020
  ident: ref_44
  article-title: Computational study on natural compounds inhibitor of c-Myc
  publication-title: Medicine
  doi: 10.1097/MD.0000000000023342
– volume: 12
  start-page: 56
  year: 2013
  ident: ref_4
  article-title: EpCAM overexpression prolongs proliferative capacity of primary human breast epithelial cells and supports hyperplastic growth
  publication-title: Mol. Cancer
  doi: 10.1186/1476-4598-12-56
– volume: 7
  start-page: 1
  year: 2017
  ident: ref_14
  article-title: Costunolide and dehydrocostus lactone combination treatment inhibit breast cancer by inducing cell cycle arrest and apoptosis through c-Myc/p53 and AKT/14-3-3 pathway
  publication-title: Sci. Rep.
– volume: 14
  start-page: 1039
  year: 1994
  ident: ref_47
  article-title: Differential regulation of the c-myc oncogene promoter by the NF-kappa B rel family of transcription factors
  publication-title: Mol. Cell. Biol.
– volume: 127
  start-page: 397
  year: 2015
  ident: ref_13
  article-title: Sesquiterpene lactones derived from Saussurealappa induce apoptosis and inhibit invasion and migration in neuroblastoma cells
  publication-title: J. Pharmacol. Sci.
  doi: 10.1016/j.jphs.2015.01.002
– volume: 31
  start-page: 1024
  year: 2008
  ident: ref_38
  article-title: Costunolide-induced apoptosis is caused by receptor-mediated pathway and inhibition of telomerase activity in NALM-6 cells
  publication-title: Biol. Pharm. Bull.
  doi: 10.1248/bpb.31.1024
– volume: 5
  start-page: 493
  year: 2014
  ident: ref_48
  article-title: NF-κB1 inhibits c-Myc protein degradation through suppression of FBW7 expression
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.1643
– volume: 5
  start-page: 30808
  year: 2020
  ident: ref_9
  article-title: In Silico Identification of Potential Phosphorylation in the Cytoplasmic Domain of Epithelial Cell Adhesion Molecule
  publication-title: ACS Omega
  doi: 10.1021/acsomega.0c02113
– volume: 275
  start-page: 36671
  year: 2000
  ident: ref_46
  article-title: NF-κB regulates transcription of the mouse telomerase catalytic subunit
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M007378200
– volume: 35
  start-page: S25
  year: 2015
  ident: ref_30
  article-title: Sustained proliferation in cancer: Mechanisms and novel therapeutic targets
  publication-title: Semin. Cancer Biol.
  doi: 10.1016/j.semcancer.2015.02.006
– volume: 47
  start-page: 6042
  year: 2004
  ident: ref_20
  article-title: Quantitative structure-activity relationship of sesquiterpene lactones as inhibitors of the transcription Factor NF-κB
  publication-title: J. Med. Chem.
  doi: 10.1021/jm049937r
– volume: 68
  start-page: 897
  year: 2016
  ident: ref_35
  article-title: Expression of epithelial cell adhesion molecule (Ep CAM) in oral squamous cell carcinoma
  publication-title: Histopathology
  doi: 10.1111/his.12870
– volume: 7
  start-page: 1
  year: 2017
  ident: ref_40
  article-title: The maintenance of telomere length in CD28+ T cells during T lymphocyte stimulation
  publication-title: Sci. Rep.
– volume: 36
  start-page: 28283
  year: 2021
  ident: ref_15
  article-title: Reviewing Leads That Promote Apoptosis-Cancer Treatment Strategies
  publication-title: Biomed. J. Sci. Tech. Res.
– volume: 9
  start-page: 1469
  year: 2018
  ident: ref_53
  article-title: Protective effects of costunolide against D-galactosamine and lipopolysaccharide-induced acute liver injury in mice
  publication-title: Front. Pharmacol.
  doi: 10.3389/fphar.2018.01469
– volume: 30
  start-page: e47
  year: 2002
  ident: ref_25
  article-title: Telomere measurement by quantitative PCR
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/30.10.e47
– volume: 282
  start-page: 20141610
  year: 2015
  ident: ref_26
  article-title: An experimental demonstration that early-life competitive disadvantage accelerates telomere loss
  publication-title: Proc. R. Soc. B Biol. Sci.
  doi: 10.1098/rspb.2014.1610
– volume: 8
  start-page: 175
  year: 2014
  ident: ref_34
  article-title: Epithelial cell adhesion molecule is overexpressed in hypopharyngeal carcinoma and suppresses the metastasis and proliferation of the disease when downregulated
  publication-title: Oncol. Lett.
  doi: 10.3892/ol.2014.2140
– volume: 5
  start-page: 4764
  year: 2014
  ident: ref_27
  article-title: Crystal structure and its bearing towards an understanding of key biological functions of EpCAM
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms5764
– ident: ref_16
  doi: 10.3390/ijms22042075
– volume: 11
  start-page: 1410
  year: 2021
  ident: ref_22
  article-title: Costunolide suppresses melanoma growth via the AKT/mTOR pathway in vitro and in vivo
  publication-title: Am. J. Cancer Res.
– volume: 80
  start-page: 253
  year: 2016
  ident: ref_24
  article-title: Costunolide, an active sesquiterpene lactone, induced apoptosis via ROS-mediated ER stress and JNK pathway in human U2OS cells
  publication-title: Biomed. Pharmacother.
  doi: 10.1016/j.biopha.2016.03.031
SSID ssj0000913814
Score 2.2095807
Snippet The epithelial cell adhesion molecule (EpCAM) is considered an essential proliferation signature in cancer. In the current research study, qPCR induced...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 2985
SubjectTerms Acute lymphoblastic leukemia
Binding sites
Breast cancer
Cell adhesion & migration
Cell adhesion molecules
Cell cycle
Cell growth
cell proliferation
costunolide
epithelial cell adhesion molecule
Epithelial cells
Gene expression
Herbal medicine
Hydrophobicity
Leukemia
Ligands
Lymphatic leukemia
Medicinal plants
Myc protein
NF-κB protein
Ovaries
Pediatrics
Phosphorylation
Proteins
Skin cancer
Software
Stem cells
Telomerase
telomerase inhibition
Telomeres
Transcription factors
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1LSyQxEA7iSQ_L6r56VyULe3APjd15TJKjM8wgC7oXBW9NHhUUhnbQcfG3-SP2N1lJt0OPCF68dqrp6kpVKpVUfUXILxC6AgP5XANKYZktbbp_j8LU1nnDrMsJsmejkwvx51JeDlp9pZywDh64E9yRrHxQWkBtY8KBEdpYbaRyMeC3o8rROvq8QTCV12BToysSXa0cx7j-qKtmz7fVd6iG6OZS--SBL8qQ_a_tM1-mSw78z-wj-dBvHOlxx_AO2YB2l2wP4AQ_kb_TRaqwmKNK0QnMkThcQToNo6ddE1ygh9PF5Pj0N50-9AmwLZ3Ylo4BSULq5AWB_ru29Gz2_3H8mVzMpueTk7JvmFB6wdmy9FpHtKcKlDTahtoEGSsboxM-MjtyXoJXUHHLMSysIZjghPLBm8BFVI7xL2SzvWnhG6EoXGct8CiTE-fgghlpGXnkegRMQ0H4s-ga36OJp6YW8wajiiTw5jWBF6RcvbXo0DTeoB-nWVnRJizs_AA1pOk1pHlLQwqy9zynTW-gdw0G45qpSmpVkJ-rYTStdF9iW7i5zzRVAnhjyMfXTgVWnPAUt0nJC6LWlGON1fWR9voqw3ejIFMDyu_v8W8_yBZL9Rh1jcvdHtlc3t7DPu6Slu4gG8QTx6IULg
  priority: 102
  providerName: Directory of Open Access Journals
Title Epithelial Cell Adhesion Molecule (EpCAM) Expression Can Be Modulated via NFκB
URI https://www.ncbi.nlm.nih.gov/pubmed/36428553
https://www.proquest.com/docview/2748270587
https://www.proquest.com/docview/2740504325
https://pubmed.ncbi.nlm.nih.gov/PMC9687693
https://doaj.org/article/50cd784e1af0431489a8957bfdccaf70
Volume 10
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1LbxMxELYgvcAB8e5CqYzEAQ6r7q7t2D6hJtqoQmpAiEq9rfwY00rRJjQp6m_rj-A34dl1QoIquO7OSrPjeXhm7G8IeQdcFaChq2tAzk1lcoP998B1aazTlbHdAdnp8OSMfzoX56ngtkzHKtc-sXPUfu6wRn4UsydVyUIo-XHxI8epUdhdTSM07pO96IKVGpC9UT398nVTZUHUS1Xy_s4ci_n9UX-rvetaL6M6xnCHY5S3YlIH3X_XfvPvY5NbcWjymDxKG0h63K_4E3IP2qfk4Ras4DPyuV7gTYtZVC06hlkk9heAVTF62g_DBfq-XoyPTz_Q-iYdhG3p2LR0BJHE40Qv8PTnpaHTya_b0XNyNqm_jU_yNDghd5xVq9wpFaJdFSCFVsaX2otQmBAsd6EyQ-sEOAkFMyymhyV47S2XzjvtGQ_SVuwFGbTzFvYJjQtsjQEWBAZzBtbroRKBBaaGUCnICFuLrnEJVRyHW8yamF2gwJu7BJ6RfPPVokfV-A_9CFdlQ4uY2N2D-dX3JplYIwrnpeJQmoCIQVxpo7SQNvj4E0EWGTlYr2mTDHXZ_FGrjLzdvI4mhn0T08L8uqMpEOitiny87FVgwwnD_E0IlhG5oxw7rO6-aS8vOhjvKEgcRPnq32y9Jg8qvHFRltGhHZDB6uoa3sR90MoeJmU_7OoIvwFvFA2X
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3dbtMwFLam7gK4QPyTMcBIIMFFtMQ_jX2B0FpadWwtCG3S7oJjH7NJVdqtHT8vxQPwEDwTPklaWjTB1W6TE8k5_nzsY_t8HyHPQagENFT7GhALw0xs8PzdC52awmpmiuqC7Kg9OBLvjuXxBvmxqIXBa5WLmFgFajexuEe-E7InxbJEquzN9CxG1Sg8XV1IaNSw2IfvX0PKNnu99zb07wvG-r3D7iBuVAViKzibx1YpH0CXQCa1Mi7VTvrEeF8I65lpF1aCzSDhhofcKQWnXSEy66x2XPisQKKDEPI3BW8nrEU2O73Rh4_LXR1k2VSpqGv0ONfJTl1FX52SzwL8w_SKss0rc2AlFXDZ-vbva5or817_FrnZLFjpbo2w22QDyjvkxgqN4V3yvjfFyo5xgDLtwjgYuxPAXTg6rMV3gb7sTbu7w1e09625eFvSrilpB4KJQwUxcPTLqaGj_q-fnXvk6Epcep-0ykkJDwkNgCqMAe4lLh44FE63lfTcc9UGpiAifOG63DYs5iimMc5DNoMOzy9zeETi5VfTmsXjP_Yd7JWlLXJwVw8m55_zZkjnMrEuUwJS45GhSChtlJZZ4V34CZ8lEdle9GneBIZZ_gfGEXm2fB2GNJ7TmBImF5VNgsRyLLTjQQ2BZUs45otS8ohka-BYa-r6m_L0pKIND45E4cutfzfrKbk2OBwe5Ad7o_1H5DrDao80DcF0m7Tm5xfwOKzB5sWTBviUfLrqsfYbQfZLmQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LbxMxELaqVEJwQLwJFDASSHBYZXdtx_YBoSZN1FIaKkSl3havPaaVok1oUh5_rT-C34RnXySoglOvu7OSd_zN2GPPzEfIC-AqBg3luQZE3KQmMnj_7rlOTG51avIyQXbS3z3i747F8Qa5aGphMK2y8Ymlo3Yzi2fkvRA9qVTGQsmer9MiDnfGb-dfI2SQwpvWhk6jgsg-_PwewrfFm72dMNcv03Q8-jTcjWqGgchyli4jq5QPAIxBCq2MS7QTPjbe59z61PRzK8BKiJlhIY5KwGmXc2md1Y5xL3NsehDc_6bEqKhDNgejyeHH9oQHO26qhFf1eozpuFdV1Jc35otgCmGpRQrnlfWwpA24bK_7d8rmyho4vkVu1ptXul2h7TbZgOIOubHS0vAu-TCaY5XHNMCaDmEahN0J4IkcPaiIeIG-Gs2H2wev6ehHnYRb0KEp6ACCiEM2MXD026mhk_Gvi8E9cnQlKr1POsWsgIeEBnDlxgDzAjcSDHKn-0p45pnqQ6qgS1ijuszWHc2RWGOahcgGFZ5dpvAuidqv5lVHj__ID3BWWlnsx10-mJ19yWrzzkRsnVQcEuOxWxFX2igtZO5d-Akv4y7ZauY0q53EIvsD6S553r4O5o13NqaA2XkpE2OTuTSM40EFgXYkDGNHIViXyDVwrA11_U1xelK2EA-KRBLMR_8e1jNyLdhY9n5vsv-YXE-x8CNJgl_dIp3l2Tk8CduxZf60xj0ln6_a1H4DSRtPzg
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Epithelial+Cell+Adhesion+Molecule+%28EpCAM%29+Expression+Can+Be+Modulated+via+NF%CE%BAB&rft.jtitle=Biomedicines&rft.au=Zia%2C+Saadiya&rft.au=Tehreem%2C+Komal&rft.au=Batool%2C+Sidra&rft.au=Ishfaq%2C+Mehreen&rft.date=2022-11-20&rft.issn=2227-9059&rft.eissn=2227-9059&rft.volume=10&rft.issue=11&rft.spage=2985&rft_id=info:doi/10.3390%2Fbiomedicines10112985&rft.externalDBID=n%2Fa&rft.externalDocID=10_3390_biomedicines10112985
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2227-9059&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2227-9059&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2227-9059&client=summon