Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches

Epithelial-mesenchymal transition (EMT) constitutes one of the hallmarks of carcinogenesis consisting in the re-differentiation of the epithelial cells into mesenchymal ones changing the cellular phenotype into a malignant one. EMT has been shown to play a role in the malignant transformation and wh...

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Main Authors: Joanna Kozak, Alicja Forma, Marcin Czeczelewski, Paweł Kozyra, Elżbieta Sitarz, Elżbieta Radzikowska-Büchner, Monika Sitarz, Jacek Baj
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/1/277
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author Joanna Kozak
Alicja Forma
Marcin Czeczelewski
Paweł Kozyra
Elżbieta Sitarz
Elżbieta Radzikowska-Büchner
Monika Sitarz
Jacek Baj
author_facet Joanna Kozak
Alicja Forma
Marcin Czeczelewski
Paweł Kozyra
Elżbieta Sitarz
Elżbieta Radzikowska-Büchner
Monika Sitarz
Jacek Baj
author_sort Joanna Kozak
collection DOAJ
description Epithelial-mesenchymal transition (EMT) constitutes one of the hallmarks of carcinogenesis consisting in the re-differentiation of the epithelial cells into mesenchymal ones changing the cellular phenotype into a malignant one. EMT has been shown to play a role in the malignant transformation and while occurring in the tumor microenvironment, it significantly affects the aggressiveness of gastric cancer, among others. Importantly, after EMT occurs, gastric cancer patients are more susceptible to the induction of resistance to various therapeutic agents, worsening the clinical outcome of patients. Therefore, there is an urgent need to search for the newest pharmacological agents targeting EMT to prevent further progression of gastric carcinogenesis and potential metastases. Therapies targeted at EMT might be combined with other currently available treatment modalities, which seems to be an effective strategy to treat gastric cancer patients. In this review, we have summarized recent advances in gastric cancer treatment in terms of targeting EMT specifically, such as the administration of polyphenols, resveratrol, tangeretin, luteolin, genistein, proton pump inhibitors, terpenes, other plant extracts, or inorganic compounds.
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spelling doaj.art-d9a80f8d711f4ff481093b9c95c393862023-11-21T03:02:30ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-12-0122127710.3390/ijms22010277Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological ApproachesJoanna Kozak0Alicja Forma1Marcin Czeczelewski2Paweł Kozyra3Elżbieta Sitarz4Elżbieta Radzikowska-Büchner5Monika Sitarz6Jacek Baj7Department of Human Anatomy, Medical University of Lublin, 20-090 Lublin, PolandDepartment of Forensic Medicine, Medical University of Lublin, 20-090 Lublin, PolandDepartment of Forensic Medicine, Medical University of Lublin, 20-090 Lublin, PolandStudent Research Group, Independent Radiopharmacy Unit, Faculty of Pharmacy, Medical University of Lublin, PL-20093 Lublin, Poland1st Department of Psychiatry, Psychotherapy and Early Intervention, Medical University of Lublin, Gluska Street 1, 20-439 Lublin, PolandDepartment of Plastic Surgery, Central Clinical Hospital of the Ministry of the Interior in Warsaw, 01-211 Warsaw, PolandDepartment of Conservative Dentistry with Endodontics, Medical University of Lublin, 20-090 Lublin, PolandDepartment of Human Anatomy, Medical University of Lublin, 20-090 Lublin, PolandEpithelial-mesenchymal transition (EMT) constitutes one of the hallmarks of carcinogenesis consisting in the re-differentiation of the epithelial cells into mesenchymal ones changing the cellular phenotype into a malignant one. EMT has been shown to play a role in the malignant transformation and while occurring in the tumor microenvironment, it significantly affects the aggressiveness of gastric cancer, among others. Importantly, after EMT occurs, gastric cancer patients are more susceptible to the induction of resistance to various therapeutic agents, worsening the clinical outcome of patients. Therefore, there is an urgent need to search for the newest pharmacological agents targeting EMT to prevent further progression of gastric carcinogenesis and potential metastases. Therapies targeted at EMT might be combined with other currently available treatment modalities, which seems to be an effective strategy to treat gastric cancer patients. In this review, we have summarized recent advances in gastric cancer treatment in terms of targeting EMT specifically, such as the administration of polyphenols, resveratrol, tangeretin, luteolin, genistein, proton pump inhibitors, terpenes, other plant extracts, or inorganic compounds.https://www.mdpi.com/1422-0067/22/1/277gastric cancerepithelial-mesenchymal transitionEMTpharmacotherapy
spellingShingle Joanna Kozak
Alicja Forma
Marcin Czeczelewski
Paweł Kozyra
Elżbieta Sitarz
Elżbieta Radzikowska-Büchner
Monika Sitarz
Jacek Baj
Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches
International Journal of Molecular Sciences
gastric cancer
epithelial-mesenchymal transition
EMT
pharmacotherapy
title Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches
title_full Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches
title_fullStr Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches
title_full_unstemmed Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches
title_short Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches
title_sort inhibition or reversal of the epithelial mesenchymal transition in gastric cancer pharmacological approaches
topic gastric cancer
epithelial-mesenchymal transition
EMT
pharmacotherapy
url https://www.mdpi.com/1422-0067/22/1/277
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AT marcinczeczelewski inhibitionorreversaloftheepithelialmesenchymaltransitioningastriccancerpharmacologicalapproaches
AT pawełkozyra inhibitionorreversaloftheepithelialmesenchymaltransitioningastriccancerpharmacologicalapproaches
AT elzbietasitarz inhibitionorreversaloftheepithelialmesenchymaltransitioningastriccancerpharmacologicalapproaches
AT elzbietaradzikowskabuchner inhibitionorreversaloftheepithelialmesenchymaltransitioningastriccancerpharmacologicalapproaches
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