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Estradiol and tamoxifen regulate endostatin generation via matrix metalloproteinase activity in breast cancer in vivo
Linköpings universitet, Institutionen för klinisk och experimentell medicin, Onkologi. Linköpings universitet, Hälsouniversitetet.
Linköpings universitet, Institutionen för klinisk och experimentell medicin, Onkologi. Linköpings universitet, Hälsouniversitetet.
2006 (engelsk)Inngår i: Cancer Research, ISSN 0008-5472, Vol. 66, nr 9, s. 4789-4794Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Matrix metalloproteinases (MMP) are important regulators of tumor progression and angiogenesis. MMPs generate both proangiogenic and antiangiogenic fragments, such as vascular endothelial growth factor and endostatin. The in vivo activation of MMPs and endostatin generation occur mainly in the extracellular environment by interactions of different cell types. Therefore, these processes are necessary to study in the extracellular space in vivo. Sex steroids play a dominant role in breast carcinogenesis, by largely unknown mechanisms. In the present study, we used in vivo microdialysis to directly quantify MMP-2 and MMP-9 activity and sample endostatin from both stroma (murine) and tumor (human) cells in vivo in solid MCF-7 tumors in nude mice. We found that tamoxifen in combination with estradiol increased tumor MMP-2/MMP-9 in vivo activity, endostatin levels, and decreased tumor vascularization compared with estradiol treatment only. The stroma-derived endostatin was three to five times higher than cancer cell–generated endostatin. After inhibition of MMP-2/MMP-9, endostatin levels decreased, providing evidence that these proteases are highly involved in the generation of endostatin. Our results support the previously reported concept that MMPs may serve as negative regulators of angiogenesis. The regulation of endostatin generation by modulation of MMP-2/MMP-9 activities suggests a previously unrecognized mechanism of estradiol and tamoxifen, which may have implications for the pathogenesis of breast cancer.

sted, utgiver, år, opplag, sider
2006. Vol. 66, nr 9, s. 4789-4794
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-14551DOI: 10.1158/0008-5472.CAN-05-4012OAI: oai:DiVA.org:liu-14551DiVA, id: diva2:23707
Tilgjengelig fra: 2007-05-30 Laget: 2007-05-30 Sist oppdatert: 2009-05-28
Inngår i avhandling
1. Effects of sex steroids and tamoxifen on matrix metalloproteinase activity and generation of endostatin in the breast
Åpne denne publikasjonen i ny fane eller vindu >>Effects of sex steroids and tamoxifen on matrix metalloproteinase activity and generation of endostatin in the breast
2007 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Sex steroids are inevitable in women. However, long-term exposure to sex steroids increases the risk of breast cancer. A complete understanding of sex steroid control of the breast and how it relates to breast cancer risk is still lacking. Angiogenesis and proteolytic enzyme activity are crucial for the process by which tumors evolve into a vascularized, invasive phenotype. Matrix metalloproteinases are potent matrixdegrading enzymes that affect several steps in tumor progression including angiogenesis. In the female reproductive organs, sex steroids regulate angiogenesis and MMP activity, yet little is known how sex steroids affect these crucial events in normal and malignant breast tissue.

This thesis elucidates a link between sex steroids, MMP activity, and angiogenesis. It is shown that estradiol down-regulates while tamoxifen up-regulates the protein expression and activity of MMP-2 and MMP-9 in human breast cancer cells in vitro and in human breast cancer xenografts in vivo. The results further suggest that a biological consequence of this regulation may be modulation of tumor angiogenesis. The net effect of adding tamoxifen to estradiol treatment was an increase in extracellular levels of the endogenous angiogenesis inhibitor endostatin and decreased levels of the tumor promoter TGF-β1 compared to estradiol treatment only. This was accompanied by reduced vasculature and decreased tumor growth. Similarly, a regulatory effect of estradiol and tamoxifen on endostatin generation was observed in normal human breast tissue by whole-tissue culture and microdialysis in human breast tissue in situ.

In conclusion, the results presented in this thesis suggest previously unknown mechanisms of action of estradiol and tamoxifen in breast cancer and in normal human breast tissue, and novel means by which estradiol may tip the scale to favor angiogenesis. This knowledge may be important for the understanding of sex steroid dependent breast carcinogenesis and in the future development of tissue-specific preventive as well as therapeutic strategies against breast cancer.

sted, utgiver, år, opplag, sider
Institutionen för biomedicin och kirurgi, 2007. s. 87
Serie
Linköping University Medical Dissertations, ISSN 0345-0082 ; 1003
Emneord
Angiogenesis, Breast cancer, TGF-β1, Endostatin, Estradiol, Mammary gland, Matrix metalloproteinases, MCF-7, Microdialysis, Nude mice, Tamoxifen
HSV kategori
Identifikatorer
urn:nbn:se:liu:diva-9015 (URN)978-91-85831-80-7 (ISBN)
Disputas
2007-06-05, Berzeliussalen, Campus US, Linköpings Universitet, Linköping, 09:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2007-05-30 Laget: 2007-05-30 Sist oppdatert: 2009-08-22

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