A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium

Background: Cyclophosphamide is widely prescribed as an anti-cancer drug and used as an immunosuppressant. Hemorrhagic cystitis is one of the common complications of cyclophosphamide intake. We hypothesized that endoplasmic reticulum stress-related proteins could be altered in urothelium treated wit...

Full description

Bibliographic Details
Main Authors: Hemalatha R, Muthuraman N, Sandya Rani, Premila Abraham
Format: Article
Language:English
Published: Mazandaran University of Medical Sciences 2023-03-01
Series:Pharmaceutical and Biomedical Research
Subjects:
Online Access:http://pbr.mazums.ac.ir/article-1-521-en.pdf
_version_ 1797796270014726144
author Hemalatha R
Muthuraman N
Sandya Rani
Premila Abraham
author_facet Hemalatha R
Muthuraman N
Sandya Rani
Premila Abraham
author_sort Hemalatha R
collection DOAJ
description Background: Cyclophosphamide is widely prescribed as an anti-cancer drug and used as an immunosuppressant. Hemorrhagic cystitis is one of the common complications of cyclophosphamide intake. We hypothesized that endoplasmic reticulum stress-related proteins could be altered in urothelium treated with cyclophosphamide.  Objectives: We checked the effect of cyclophosphamide on the expression of various endoplasmic reticulum stress-related proteins in Vero cells.  Methods: We treated Vero cells with varying doses of cyclophosphamide and observed its viability in flow cytometry using propidium iodide staining. We looked for changes in the expression of endoplasmic reticulum stress-related proteins in Vero cells treated with cyclophosphamide by western blot technique.  Results: Cyclophosphamide at higher doses caused more death in Vero cells that could be attributed to an increase in apoptosis as evidenced by the changes in the morphology of cells and increased expression of endoplasmic reticulum specific caspase-12 proteins. Growth arrest/DNA damage 153 (GADD 153), one of the key transcription factors involved in the mediation of endoplasmic reticulum stress and apoptosis, was upregulated in Vero cells treated with cyclophosphamide. The protective effect of glucose-regulated protein GRP 78 against apoptosis was lost in Vero cells treated with a higher dose of cyclophosphamide, which is corroborated by decreased expression of GRP 78 in Vero cells treated with higher doses compared to Vero cells treated with lower doses of cyclophosphamide. Expression of disulfide isomerase protein, which guides misfolded proteins to fold properly, was downregulated in Vero cells treated with cyclophosphamide.  Conclusion: To summarize, our study showed an alteration in the expression of key endoplasmic reticulum stress-related proteins in Vero cells treated with cyclophosphamide.
first_indexed 2024-03-13T03:30:33Z
format Article
id doaj.art-923137e02ed84c11a25c7699a8aabc72
institution Directory Open Access Journal
issn 2423-4494
language English
last_indexed 2024-03-13T03:30:33Z
publishDate 2023-03-01
publisher Mazandaran University of Medical Sciences
record_format Article
series Pharmaceutical and Biomedical Research
spelling doaj.art-923137e02ed84c11a25c7699a8aabc722023-06-24T09:03:58ZengMazandaran University of Medical SciencesPharmaceutical and Biomedical Research2423-44942023-03-0192153162A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to UrotheliumHemalatha R0Muthuraman N1Sandya Rani2Premila Abraham3 Department of Biochemistry, Tata Medical Cancer Centre, Kolkata, West Bengal, India. Department of Biochemistry, Christian Medical College, Vellore, Tamil Nadu, India. Centre for Stem Cell Research, Bagayam, Vellore, Tamil Nadu, India. Department of Biochemistry, Christian Medical College, Vellore, Tamil Nadu, India. Background: Cyclophosphamide is widely prescribed as an anti-cancer drug and used as an immunosuppressant. Hemorrhagic cystitis is one of the common complications of cyclophosphamide intake. We hypothesized that endoplasmic reticulum stress-related proteins could be altered in urothelium treated with cyclophosphamide.  Objectives: We checked the effect of cyclophosphamide on the expression of various endoplasmic reticulum stress-related proteins in Vero cells.  Methods: We treated Vero cells with varying doses of cyclophosphamide and observed its viability in flow cytometry using propidium iodide staining. We looked for changes in the expression of endoplasmic reticulum stress-related proteins in Vero cells treated with cyclophosphamide by western blot technique.  Results: Cyclophosphamide at higher doses caused more death in Vero cells that could be attributed to an increase in apoptosis as evidenced by the changes in the morphology of cells and increased expression of endoplasmic reticulum specific caspase-12 proteins. Growth arrest/DNA damage 153 (GADD 153), one of the key transcription factors involved in the mediation of endoplasmic reticulum stress and apoptosis, was upregulated in Vero cells treated with cyclophosphamide. The protective effect of glucose-regulated protein GRP 78 against apoptosis was lost in Vero cells treated with a higher dose of cyclophosphamide, which is corroborated by decreased expression of GRP 78 in Vero cells treated with higher doses compared to Vero cells treated with lower doses of cyclophosphamide. Expression of disulfide isomerase protein, which guides misfolded proteins to fold properly, was downregulated in Vero cells treated with cyclophosphamide.  Conclusion: To summarize, our study showed an alteration in the expression of key endoplasmic reticulum stress-related proteins in Vero cells treated with cyclophosphamide.http://pbr.mazums.ac.ir/article-1-521-en.pdfcyclophosphamidecystitisendoplasmic reticulum stresscaspase-12protein disulfide isomerasesendoplasmic reticulum chaperone bip
spellingShingle Hemalatha R
Muthuraman N
Sandya Rani
Premila Abraham
A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium
Pharmaceutical and Biomedical Research
cyclophosphamide
cystitis
endoplasmic reticulum stress
caspase-12
protein disulfide isomerases
endoplasmic reticulum chaperone bip
title A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium
title_full A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium
title_fullStr A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium
title_full_unstemmed A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium
title_short A Study on the Alteration of Endoplasmic Reticulum Stress-related Proteins in Cyclophosphamide-induced Damage to Urothelium
title_sort study on the alteration of endoplasmic reticulum stress related proteins in cyclophosphamide induced damage to urothelium
topic cyclophosphamide
cystitis
endoplasmic reticulum stress
caspase-12
protein disulfide isomerases
endoplasmic reticulum chaperone bip
url http://pbr.mazums.ac.ir/article-1-521-en.pdf
work_keys_str_mv AT hemalathar astudyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT muthuramann astudyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT sandyarani astudyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT premilaabraham astudyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT hemalathar studyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT muthuramann studyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT sandyarani studyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium
AT premilaabraham studyonthealterationofendoplasmicreticulumstressrelatedproteinsincyclophosphamideinduceddamagetourothelium