Role of manganese superoxide dismutase on growth and invasive properties of human estrogen-independent breast cancer cells

Manganese superoxide dismutase (MnSOD) is known to play a role in cancer. MnSOD exerts a tumor suppressive effect in estrogen-dependent human breast cancer cells. In the present study we investigated the in vitro role of MnSOD in the growth of some aggressive and highly metastatic estrogen-independe...

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Published in:Breast cancer research and treatment Vol. 108; no. 2; pp. 203 - 215
Main Authors: Kattan, Zilal, Minig, Vanessa, Leroy, Pierre, Dauça, Michel, Becuwe, Philippe
Format: Journal Article
Language:English
Published: Boston Springer US 01-03-2008
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Abstract Manganese superoxide dismutase (MnSOD) is known to play a role in cancer. MnSOD exerts a tumor suppressive effect in estrogen-dependent human breast cancer cells. In the present study we investigated the in vitro role of MnSOD in the growth of some aggressive and highly metastatic estrogen-independent breast cancer cells, i.e., MDA-MB231 and SKBR3 cells. We show that estrogen-independent cells expressed a significantly higher basal MnSOD level compared to estrogen-dependent human breast cancer cell lines (MCF-7 and T47D). For MDA-MB231 cells, the high-MnSOD level was accompanied by an overproduction of intracellular hydrogen peroxide (H 2 O 2 ) and by a low expression of the major H 2 O 2 -detoxifying enzymes, catalase, and peroxiredoxin 3, compared to MCF-7 cells. Suppression of MnSOD expression by antisense RNA was associated with a decrease of H 2 O 2 content and caused a stimulation of growth with a reduced cell doubling time but induced a decrease of colony formation. Furthermore, treatment of MDA-MB231 cells with H 2 O 2 scavengers markedly reduced tumor cell growth and colony formation. In addition, MnSOD suppression or treatment with H 2 O 2 scavengers reduced the invasive properties of MDA-MB231 cells up to 43%, with a concomitant decrease of metalloproteinase-9 activity. We conclude that MnSOD plays a role in regulating tumor cell growth and invasive properties of estrogen-independent metastatic breast cancer cells. These action are mediated by MnSOD-dependent H 2 O 2 production. In addition, these results suggest that MnSOD up-regulation may be one mechanism that contributes to the development of metastatic breast cancers.
AbstractList Manganese superoxide dismutase (MnSOD) is known to play a role in cancer. MnSOD exerts a tumor suppressive effect in estrogen-dependent human breast cancer cells. In the present study we investigated the in vitro role of MnSOD in the growth of some aggressive and highly metastatic estrogen-independent breast cancer cells, i.e., MDA-MB231 and SKBR3 cells. We show that estrogen-independent cells expressed a significantly higher basal MnSOD level compared to estrogen-dependent human breast cancer cell lines (MCF-7 and T47D). For MDA-MB231 cells, the high-MnSOD level was accompanied by an overproduction of intracellular hydrogen peroxide (H2O2) and by a low expression of the major H2O2-detoxifying enzymes, catalase, and peroxiredoxin 3, compared to MCF-7 cells. Suppression of MnSOD expression by antisense RNA was associated with a decrease of H2O2 content and caused a stimulation of growth with a reduced cell doubling time but induced a decrease of colony formation. Furthermore, treatment of MDA-MB231 cells with H2O2 scavengers markedly reduced tumor cell growth and colony formation. In addition, MnSOD suppression or treatment with H2O2 scavengers reduced the invasive properties of MDA-MB231 cells up to 43%, with a concomitant decrease of metalloproteinase-9 activity. We conclude that MnSOD plays a role in regulating tumor cell growth and invasive properties of estrogen-independent metastatic breast cancer cells. These action are mediated by MnSOD-dependent H2O2 production. In addition, these results suggest that MnSOD up-regulation may be one mechanism that contributes to the development of metastatic breast cancers.
Manganese superoxide dismutase (MnSOD) is known to play a role in cancer. MnSOD exerts a tumor suppressive effect in estrogen-dependent human breast cancer cells. In the present study we investigated the in vitro role of MnSOD in the growth of some aggressive and highly metastatic estrogen-independent breast cancer cells, i.e., MDA-MB231 and SKBR3 cells. We show that estrogen-independent cells expressed a significantly higher basal MnSOD level compared to estrogen-dependent human breast cancer cell lines (MCF-7 and T47D). For MDA-MB231 cells, the high-MnSOD level was accompanied by an overproduction of intracellular hydrogen peroxide (H 2 O 2 ) and by a low expression of the major H 2 O 2 -detoxifying enzymes, catalase, and peroxiredoxin 3, compared to MCF-7 cells. Suppression of MnSOD expression by antisense RNA was associated with a decrease of H 2 O 2 content and caused a stimulation of growth with a reduced cell doubling time but induced a decrease of colony formation. Furthermore, treatment of MDA-MB231 cells with H 2 O 2 scavengers markedly reduced tumor cell growth and colony formation. In addition, MnSOD suppression or treatment with H 2 O 2 scavengers reduced the invasive properties of MDA-MB231 cells up to 43%, with a concomitant decrease of metalloproteinase-9 activity. We conclude that MnSOD plays a role in regulating tumor cell growth and invasive properties of estrogen-independent metastatic breast cancer cells. These action are mediated by MnSOD-dependent H 2 O 2 production. In addition, these results suggest that MnSOD up-regulation may be one mechanism that contributes to the development of metastatic breast cancers.
Manganese superoxide dismutase (MnSOD) is known to play a role in cancer. MnSOD exerts a tumor suppressive effect in estrogen-dependent human breast cancer cells. In the present study we investigated the in vitro role of MnSOD in the growth of some aggressive and highly metastatic estrogen-independent breast cancer cells, i.e., MDA-MB231 and SKBR3 cells. We show that estrogen-independent cells expressed a significantly higher basal MnSOD level compared to estrogen-dependent human breast cancer cell lines (MCF-7 and T47D). For MDA-MB231 cells, the high-MnSOD level was accompanied by an overproduction of intracellular hydrogen peroxide (H2O2) and by a low expression of the major H2O2-detoxifying enzymes, catalase, and peroxiredoxin 3, compared to MCF-7 cells. Suppression of MnSOD expression by antisense RNA was associated with a decrease of H2O2 content and caused a stimulation of growth with a reduced cell doubling time but induced a decrease of colony formation. Furthermore, treatment of MDA-MB231 cells with H2O2 scavengers markedly reduced tumor cell growth and colony formation. In addition, MnSOD suppression or treatment with H2O2 scavengers reduced the invasive properties of MDA-MB231 cells up to 43%, with a concomitant decrease of metalloproteinase-9 activity. We conclude that MnSOD plays a role in regulating tumor cell growth and invasive properties of estrogen-independent metastatic breast cancer cells. These action are mediated by MnSOD-dependent H2O2 production. In addition, these results suggest that MnSOD up-regulation may be one mechanism that contributes to the development of metastatic breast cancers. [PUBLICATION ABSTRACT]
Author Dauça, Michel
Leroy, Pierre
Becuwe, Philippe
Kattan, Zilal
Minig, Vanessa
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  givenname: Pierre
  surname: Leroy
  fullname: Leroy, Pierre
  organization: Laboratoire de Chimie Physique et Microbiologie pour l’Environnement, UMR 7564 CNRS Nancy-Université, Faculté de Pharmacie
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  givenname: Michel
  surname: Dauça
  fullname: Dauça, Michel
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  surname: Becuwe
  fullname: Becuwe, Philippe
  email: Philippe.Becuwe@scbiol.uhp-nancy.fr
  organization: Laboratoire de Biologie Cellulaire du Développement, EA 3446-IFR111 (Proliférateurs de Peroxysomes), Université Henri Poincaré-Nancy I, Faculté des Sciences
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IsPeerReviewed true
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Issue 2
Keywords Cell growth
Reactive oxygen species
Matrix metalloproteinases
Invasiveness
Breast cancer
Metastasis
Manganese superoxide dismutase
Human
Cell proliferation
Oxidative stress
Breast disease
Enzyme
Growth
Estrogen
Manganese superoxide dismutase, Breast cancer, Cell growth, Invasiveness, Metastasis
Metalloendopeptidases
Superoxide dismutase
Malignant tumor
Ovarian hormone
Mammary gland diseases
Peptidases
Hydrolases
Oxidoreductases
Sex steroid hormone
Tumor cell
Cancer
Language English
License CC BY 4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c465t-4685b0579dd230e10416378004bf9ab71839d75e8907ea168a8928a7e3fbfb2c3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 17473980
PQID 212480130
PQPubID 36266
PageCount 13
ParticipantIDs proquest_miscellaneous_70326750
proquest_journals_212480130
crossref_primary_10_1007_s10549_007_9597_5
pubmed_primary_17473980
pascalfrancis_primary_20207431
springer_journals_10_1007_s10549_007_9597_5
PublicationCentury 2000
PublicationDate 2008-03-01
PublicationDateYYYYMMDD 2008-03-01
PublicationDate_xml – month: 03
  year: 2008
  text: 2008-03-01
  day: 01
PublicationDecade 2000
PublicationPlace Boston
PublicationPlace_xml – name: Boston
– name: Dordrecht
– name: Netherlands
PublicationTitle Breast cancer research and treatment
PublicationTitleAbbrev Breast Cancer Res Treat
PublicationTitleAlternate Breast Cancer Res Treat
PublicationYear 2008
Publisher Springer US
Springer
Springer Nature B.V
Publisher_xml – name: Springer US
– name: Springer
– name: Springer Nature B.V
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Snippet Manganese superoxide dismutase (MnSOD) is known to play a role in cancer. MnSOD exerts a tumor suppressive effect in estrogen-dependent human breast cancer...
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SubjectTerms Antioxidants - pharmacology
Biological and medical sciences
Breast cancer
Breast Neoplasms - enzymology
Breast Neoplasms - genetics
Breast Neoplasms - pathology
Cancer research
Cancer therapies
Catalase - metabolism
Cell growth
Cell Line, Tumor
Cell Movement - drug effects
Cell Proliferation - drug effects
Down-Regulation
Enzymes
Estrogens
Estrogens - metabolism
Female
Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Neoplastic
Gynecology. Andrology. Obstetrics
Humans
Hydrogen Peroxide - metabolism
Mammary gland diseases
Matrix Metalloproteinase 9 - metabolism
Medical sciences
Medicine
Medicine & Public Health
Neoplasm Invasiveness
Oncology
Pathology
Peroxiredoxin III
Peroxiredoxins - metabolism
Preclinical Study
RNA, Antisense - metabolism
Superoxide Dismutase - genetics
Superoxide Dismutase - metabolism
Time Factors
Transfection
Tumors
Title Role of manganese superoxide dismutase on growth and invasive properties of human estrogen-independent breast cancer cells
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https://www.ncbi.nlm.nih.gov/pubmed/17473980
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https://search.proquest.com/docview/70326750
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