Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>

Objective: Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer related deaths. Despite the advancements in cancer management, novel targets to improve treatment outcomes for PDAC are still needed. Herein, we aimed to evaluate the anti-cancer efficacy of nonselective non-ste...

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Main Authors: Ayşe Nur Çaldıran, Gizem Gürel, Başak Aru
Format: Article
Language:English
Published: Galenos Publishing House 2024-12-01
Series:Turkish Journal of Immunology
Subjects:
Online Access:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tji&un=TJI-29290
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author Ayşe Nur Çaldıran
Gizem Gürel
Başak Aru
author_facet Ayşe Nur Çaldıran
Gizem Gürel
Başak Aru
author_sort Ayşe Nur Çaldıran
collection DOAJ
description Objective: Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer related deaths. Despite the advancements in cancer management, novel targets to improve treatment outcomes for PDAC are still needed. Herein, we aimed to evaluate the anti-cancer efficacy of nonselective non-steroidal anti-inflammatory drug (NSAID) diclofenac on PDAC in vitro, either alone or in combination with starvation. Materials and Methods: Two different PDAC cell lines, PANC-1 and MIA PaCa-2, were treated with diclofenac either alone or after starvation with culture medium or Hank's balanced salt solution. Apoptosis, autophagy and cyclooxygenase (COX) levels were evaluated by flow cytometry. Results: Diclofenac decreased both COX isoforms compared to untreated cells. However, the differences in COX-2 levels between starvation modalities were not significant. Furthermore, starvation followed by diclofenac treatment did not decrease COX-2 levels in the PDAC cell lines tested compared to diclofenac treatment alone. Conclusion: This study demonstrated that diclofenac treatment can induce apoptosis in PDAC by suppressing both COX-1 and COX-2 levels, although starvation does not have a major impact on its anticancer efficacy. Further studies should focus on determining the optimal duration of starvation prior to NSAID treatment. In addition, the combinatorial effects of starvation and NSAID treatment with conventional treatment options for PDAC should be evaluated.
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publishDate 2024-12-01
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spelling doaj-art-07a67ee18e73499885dec2d36c973afc2025-01-17T08:29:34ZengGalenos Publishing HouseTurkish Journal of Immunology1301-109X2147-83252024-12-0112311412410.4274/tji.galenos.2025.29290TJI-29290Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>Ayşe Nur Çaldıran0Gizem Gürel1Başak Aru2Yeditepe University Faculty of Medicine, Department of Immunology, İstanbul, TurkeyYeditepe University Faculty of Medicine, Department of Immunology, İstanbul, TurkeyYeditepe University Faculty of Medicine, Department of Immunology, İstanbul, TurkeyObjective: Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer related deaths. Despite the advancements in cancer management, novel targets to improve treatment outcomes for PDAC are still needed. Herein, we aimed to evaluate the anti-cancer efficacy of nonselective non-steroidal anti-inflammatory drug (NSAID) diclofenac on PDAC in vitro, either alone or in combination with starvation. Materials and Methods: Two different PDAC cell lines, PANC-1 and MIA PaCa-2, were treated with diclofenac either alone or after starvation with culture medium or Hank's balanced salt solution. Apoptosis, autophagy and cyclooxygenase (COX) levels were evaluated by flow cytometry. Results: Diclofenac decreased both COX isoforms compared to untreated cells. However, the differences in COX-2 levels between starvation modalities were not significant. Furthermore, starvation followed by diclofenac treatment did not decrease COX-2 levels in the PDAC cell lines tested compared to diclofenac treatment alone. Conclusion: This study demonstrated that diclofenac treatment can induce apoptosis in PDAC by suppressing both COX-1 and COX-2 levels, although starvation does not have a major impact on its anticancer efficacy. Further studies should focus on determining the optimal duration of starvation prior to NSAID treatment. In addition, the combinatorial effects of starvation and NSAID treatment with conventional treatment options for PDAC should be evaluated.https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tji&un=TJI-29290pancreatic ductal adenocarcinomacyclooxygenasesnon-steroidal anti-inflammatory drugsapoptosisautophagy
spellingShingle Ayşe Nur Çaldıran
Gizem Gürel
Başak Aru
Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>
Turkish Journal of Immunology
pancreatic ductal adenocarcinoma
cyclooxygenases
non-steroidal anti-inflammatory drugs
apoptosis
autophagy
title Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>
title_full Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>
title_fullStr Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>
title_full_unstemmed Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>
title_short Evaluation of the Anti-Cancer Efficacy of Cyclooxygenase Inhibition in Combination with Nutrient Starvation on Pancreatic Ductal Adenocarcinoma <em>In Vitro</em>
title_sort evaluation of the anti cancer efficacy of cyclooxygenase inhibition in combination with nutrient starvation on pancreatic ductal adenocarcinoma em in vitro em
topic pancreatic ductal adenocarcinoma
cyclooxygenases
non-steroidal anti-inflammatory drugs
apoptosis
autophagy
url https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tji&un=TJI-29290
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