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 |
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Main Authors: | , , , , |
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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 |
Author_xml | – sequence: 1 givenname: Zilal surname: Kattan fullname: Kattan, Zilal organization: Laboratoire de Biologie Cellulaire du Développement, EA 3446-IFR111 (Proliférateurs de Peroxysomes), Université Henri Poincaré-Nancy I, Faculté des Sciences – sequence: 2 givenname: Vanessa surname: Minig fullname: Minig, Vanessa organization: Laboratoire de Biologie Cellulaire du Développement, EA 3446-IFR111 (Proliférateurs de Peroxysomes), Université Henri Poincaré-Nancy I, Faculté des Sciences – sequence: 3 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 – sequence: 4 givenname: Michel surname: Dauça fullname: Dauça, Michel organization: Laboratoire de Biologie Cellulaire du Développement, EA 3446-IFR111 (Proliférateurs de Peroxysomes), Université Henri Poincaré-Nancy I, Faculté des Sciences – sequence: 5 givenname: Philippe 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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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 |
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PublicationTitle | Breast cancer research and treatment |
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Publisher | Springer US Springer 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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