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...
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Published in | Biomedicines Vol. 10; no. 11; p. 2985 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
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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. |
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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 |
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Keywords | costunolide cell proliferation acute lymphoblastic leukemia telomerase inhibition epithelial cell adhesion molecule |
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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 |
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Title | Epithelial Cell Adhesion Molecule (EpCAM) Expression Can Be Modulated via NFκB |
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