نتایج جستجو برای: t47

تعداد نتایج: 93  

Eskandar Alipour Susan Kabudanian Ardestani Tina Shojaie Zinatsadat Mousavi

In this investigation, new structures based on homoisoflavonoids were designed. Homoisoflavonoids are considered as an important class of flavonoids with various biological properties such as cytotoxicity. A new series of benzylidene-6,7-dihydro-8H-[1,3]dioxolo[4,5-g] chromen-8-one derivatives were developed and their cytotoxic activities evaluated for all compounds on three human breast cancer...

Journal: :PLoS ONE 2008
Xiao-Dong Fu Maria S. Giretti Chiara Baldacci Silvia Garibaldi Marina Flamini Angel Matias Sanchez Angiolo Gadducci Andrea R. Genazzani Tommaso Simoncini

Progesterone plays a role in breast cancer development and progression but the effects on breast cancer cell movement or invasion have not been fully explored. In this study, we investigate the actions of natural progesterone and of the synthetic progestin medroxyprogesterone acetate (MPA) on actin cytoskeleton remodeling and on breast cancer cell movement and invasion. In particular, we charac...

Journal: :Molecular cancer therapeutics 2012
Alla Polotskaia Sandy Hoffman Nancy L Krett Mala Shanmugam Steven T Rosen Jill Bargonetti

8-Amino-adenosine (8-NH(2)-Ado) is a ribose sugar nucleoside analogue that reduces cellular ATP levels and inhibits mRNA synthesis. Estrogen receptor-negative (ER-) metastatic breast cancers often contain mutant p53; therefore, we asked if 8-NH(2)-Ado could kill breast cancer cells without activating the p53-pathway. Regardless of the breast cancer subtype tested or the p53 status of the cells,...

Journal: :PloS one 2015
Sarah L Shafer Patrick J Bartlein Elizabeth M Gray Richard T Pelltier

Future climate change may significantly alter the distributions of many plant taxa. The effects of climate change may be particularly large in mountainous regions where climate can vary significantly with elevation. Understanding potential future vegetation changes in these regions requires methods that can resolve vegetation responses to climate change at fine spatial resolutions. We used LPJ,...

1999
M. Kandouz A. Lombet J-Y. Perrot D. Jacob S. Carvajal A. Kazem W. Rostene A. Therwath A. Gompel

The promoting action of E2 in breast cancer cells has been, until now, mainly linked to its action on proli®eration. Because of the importance of an increase in apoptosis in breast cancer prevention, we have studied the possible e€ects of various antiestrogens, progestins and an androgen on its occurrence in three hormone-dependent breast cancer cell lines. The antiestrogens were, a triphenylet...

Journal: :Anticancer research 2009
Subhani M Okarvi Ibrahim A Jammaz

HER2/neu and MUC1-based synthetic peptides were prepared and evaluated in an effort to develop peptide-based radiopharmaceuticals derived from tumor-associated-antigens for the detection of breast cancer. The receptors for HER2/neu and MUC1 are overexpressed in various human cancers, such as breast and ovarian cancer. The relatively low expression of these antigens on normal tissues makes them ...

Journal: :Endocrine-related cancer 2006
Yayun Liang Rolf A Brekken Salman M Hyder

Increased levels of vascular endothelial growth factor (VEGF) are associated with a poor response of breast cancer to anti-hormone treatment. Although VEGF is regarded as an endothelial-specific growth factor, recent reports have shown that VEGF can promote proliferation of other cell types, including breast tumor cells. We have characterized the proliferative effects of VEGF in breast cancer c...

2015
Matthew T. Cook Yayun Liang Cynthia Besch-Williford Sandy Goyette Benford Mafuvadze Salman M. Hyder

PURPOSE Clinical trials and epidemiological evidence have shown that combined estrogen/progestin hormone replacement therapy, but not estrogen therapy alone, increases breast cancer risk in post-menopausal women. Previously we have shown that natural and synthetic progestins, including the widely used synthetic progestin medroxyprogesterone acetate (MPA), increase production of a potent angioge...

2012
Alla Polotskaia Sandy Hoffman Nancy L. Krett Mala Shanmugam Steven T. Rosen Jill Bargonetti

8-Amino-adenosine (8-NH2-Ado) is a ribose sugar nucleoside analogue that reduces cellular ATP levels and inhibits mRNA synthesis. Estrogen receptor-negative (ER ) metastatic breast cancers often contain mutant p53; therefore, we asked if 8-NH2-Ado could kill breast cancer cells without activating the p53-pathway. Regardless of the breast cancer subtype tested or the p53 status of the cells, 8-N...

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