Zobrazeno 1 - 10
of 11
pro vyhledávání: '"R M, O'Regan"'
Autor:
R M, O'Regan, A, Cisneros, G M, England, J I, MacGregor, H D, Muenzner, V J, Assikis, M M, Bilimoria, M, Piette, Y P, Dragan, H C, Pitot, R, Chatterton, V C, Jordan
Publikováno v:
JNCI Journal of the National Cancer Institute. 90:1552-1558
Background Tamoxifen has been shown to promote the growth of human endometrial tumors implanted in athymic mice, and it has been associated with a twofold to threefold increase in endometrial cancer. Toremifene, a chlorinated derivative of tamoxifen,
Autor:
F R Khuri, R M O'Regan
Publikováno v:
Endocrine-related cancer. 11(2)
The ras family of proto-oncogenes are upstream mediators of several essential cellular signal transduction pathways involved in cell proliferation and survival. Point mutations of ras oncogenes result in constitutively active Ras and have been shown
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(12)
Arzoxifene (Arzox) is a novel benzothiophene analogue with selective estrogen receptor modulator activity similar to raloxifene. Arzox is being developed as a treatment for breast cancer and has a predominantly antiestrogenic effect on the rodent ute
Autor:
R M, O'Regan, W J, Gradishar
Publikováno v:
Oncology (Williston Park, N.Y.). 15(9)
Tamoxifen (Nolvadex), a selective estrogen-receptor modulator, or SERM, is currently the endocrine therapy of choice for all stages of hormone-responsive breast cancer. Only tamoxifen has been approved by the US Food and Drug Administration to reduce
Autor:
R M, O'Regan, V C, Jordan
Publikováno v:
Cancer treatment and research. 106
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(12)
The triphenylethylene antiestrogens, idoxifene (Idox) and toremifene (Tor), are structurally related analogues of tamoxifen (Tam) and were developed to improve the therapeutic index for advanced breast cancer patients. However, the issue of cross-res
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(11)
MCF-7 cells are used routinely to study tamoxifen-stimulated drug resistance in vivo. However, unlike MCF-7 cells, T47D cells express mutant p53 protein and lose the estrogen receptor (ER) during long-term estrogen deprivation in vitro [Pink et al.,
Autor:
R M, O'Regan
Publikováno v:
Cancer treatment and research. 103
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(5)
The estrogen receptor (ER)-positive MCF-7 breast cancer cell line can be transplanted into athymic mice and grown into tumors with estradiol (E2) support. Tamoxifen (TAM) blocks E2-stimulated tumor growth; however, continuous TAM treatment results in
Autor:
R. M. O'Regan, V. C. Jordan
Publikováno v:
JNCI Journal of the National Cancer Institute. 91:722-723