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Human breast cancer cell lines

WS-7528 [132147-69-4][VI] a nonsteroidal estrogen, is an isoflavone which has been isolated from Streptomjces sp. No. 7528 and is an estrogen agonist. It inhibits [3ff]-estradiol binding to its receptor in rat uterine cytosol at an inhibitor for 50% of the rats tested (IC q) concentration of 5.7 nM. It also induces the growth of estrogen-dependent human breast cancer cell line MCE-7 (7). [Pg.233]

Hsu J-T, Ying C, Lan H-C. 1998. The effects of pesticides chlordane, dieldrin and endosulfan on the growth of human breast cancer cell lines MCF-7 and SK-BR-3. J Chinese Agri Chem Soc 36(6) 535-546. [Pg.299]

Pihie AHL, Stanslas J, Din LB. Non-steroid receptor-mediated anti-proliferative activity of styrylpyrone derivative in human breast cancer cell lines. Anticancer Res 1998 18 1739-1743. [Pg.228]

Lee ATC, Azimahtol HLP, Tan AN. Styrylpyrone derivatives (SPD) induces apopotosis in caspases-7-dependent manner in the human breast cancer cell line MCF-7. Cancer Cell Int 2003 3 1-8. [Pg.228]

Another peculiarity of the study is that the use of a biological system has allowed the authors to hypothesize a possible mechanism of action of the leachate as a mixture, hypothesis that could have been drafted on the basis of the only knowledge derived by chemical analysis. Researchers suggest that leachate inhibits cell proliferation at low doses probably inducing a reversible cell cycle arrest that becomes irreversible at high doses, probably due to leachate-induced oxidative stress. This activity is mainly due to the chemical compounds extracted in the aqueous phase. Similar effects were noticed by previous investigations on other human cells (human peripheral blood lymphocytes and a human breast cancer cell line, MCF-7) [31, 32], supporting the hypothesis that cells that survive the initial insult from leachate constituents maintains the potential to proliferate until the effects on cell metabolism lead to death. [Pg.180]

Identification Annotation and Data Correlation in MCF10 Human Breast Cancer Cell Lines... [Pg.235]

Wang K, Ramji S, Bhathena A et al. Glutathione S-transferases in wild-type and doxorubicin-resistant MCF-7 human breast cancer cell lines. Xenobiotica 1999 ... [Pg.308]

Chong BE, Lubman DM, Miller FR, et al. Rapid screening of protein profiles of human breast cancer cell lines using non-porous reversed-phase high performance liquid chromatography separation with matrix-assisted laser desorption/ionization time-of-flight mass spectral analysis. Rapid Commun. Mass Spectrom. 1999 13 1808-1812. [Pg.247]

Seiler-Tuyns A, Walker P, Martinez E, Merillat AM, Givel F, Wahli W (1986) Identification of estrogen-responsive DNA sequences by transient expression experiments in a human breast cancer cell line. Nucleic Acids Res 14 8755... [Pg.61]

Experimental studies showed antitumoral effects of raloxifene in different in vitro preparations and animal models. Raloxifene has been able to inhibit the mitogenic effect induced by estrogens on ZR-75-1 cells, an estrogen responsive human breast cancer cell line (Poulin et al. 1989). In a well-accepted rat model of breast cancer induced by nitroso-methyl urea (NMU) raloxifene significantly suppressed the development of breast tumors and acted synergistically with 9 cis-retinoic acid (Anzano et al. 1996). [Pg.264]

Novel macrocyclic and open-chain taxoid mimicking compounds were synthesized. Two of these, compounds 283 and 284, were found to possess cytotoxicity with micromolar level IC50 values against human breast cancer cell lines <2004BML3491>. [Pg.399]

J. A. Engelman, X. L. Zhang, and M. P. Lisanti. Methylation of a CpG island in the 5 promoter region of the caveolin-1 gene in human breast cancer cell lines. FEBS Lett. 448 221-230 (1999). [Pg.612]

Brown, A.M.C., Jeltsch, J.M., Roberts, M. and Chambon, P. (1984). Activation of the PS2 gene transcription is a primary response to estrogen in human breast cancer cell line MCF-7, Proc. Natl. Acad. Sci. U.S.A., 81, 6344-6348. [Pg.105]

Diel, P., Olff, S., Schmidt, S. and Michna, FI. (2001). Molecular identification of potential selective estrogen receptor modulator (SERM) like properties of phytoestrogens in the human breast cancer cell line MCF-7, Planta Med., Aug, 67, 6, 510-514. [Pg.105]

Pledgie-Tracy A, Sobolewski MD, Davidson NE. (2007) Sulforaphane induces cell type-specific apoptosis in human breast cancer cell lines. Mol Cancer Ther 6 1013-1021. [Pg.303]

Bouras etal. (2002) undertook a comprehensive study of differential expression focused upon genes associated with estrogen responsiveness (ER+) in a human breast cancer cell line correlated with clinical tumor... [Pg.173]

PPl (8) and its pyrazolopyrimidine analog PP2 (9) [99-108] were first described as potent inhibitors of SFKs with marked selectivity versus ZAP-70, JAK2, EGF-R, and PKA kinases. PPl provided an early key inhibitor of Src kinase to enable determination of its roles in VEGF-mediated angiogenesis and vascular permeability, Src-driven human breast cancer cell lines with respect to both heregulin-dependent or independent growth, and Src-related,... [Pg.395]

Kennedy MJ, Prestigiacomo LJ, Tyler G, May WS, Davidson NE (1992) Differential effects of bryostatin 1 and phorbol ester on human breast cancer cell lines. Cancer Res 52 1278-1283... [Pg.77]

Investigators found that human breast cancer cell lines with BRCAl mutations showed a twofold to fourfold increase in apoptosis after treatment with ionizing radiation, cisplatin, or doxorubicin, compared with cells free of mutations. They also found that BRCAl tumor cell lines were resistant to other agents, such as paclitaxel (Taxol) and docetaxel (Taxotere), treatments used commonly in ovarian cancer and advanced-stage breast cancers. [Pg.392]

Hsu, . C., Li-Chan, E. C. Y., and Jao, C. L. (2011). Antiproliferative activity of peptides prepared from enzymatic hydrolysates of tuna dark muscle on human breast cancer cell line MCF-7. Food Chem. 126, 617-622. [Pg.246]

Picot, L., Bordenave, S., Didelot, S., Fruitier-Arnaudin, I., Sannier, F., Thorkelsson, G., Berge, J. P., Guerard, F., Chabeaud, A., and Piot, J. M. (2006). Antiproliferative activity of fish protein hydrolysates on human breast cancer cell lines. Process Biochem. 41, 1217-1222. [Pg.247]

Panjehpour M, Karami-Tehrani F (2007) Adenosine modulates cell growth in the human breast cancer cells via adenosine receptors. Oncol Res 16(12) 575—585 Panjehpour M, Karami-Tehrani F (2004) An adenosine analog (IB-MECA) inhibits anchorage-dependent cell growth of various human breast cancer cell lines. Int J Biochem Cell Biol 36(8) 1502—1509... [Pg.316]

Pec MK, Moser-Thier K, Fernandez JJ, Souto ML, Kubista E (1999) Growth Inhibition by Dehydrothyrsiferol - A Non-Pgp Modulator, Derived from a Marine Red Alga - in Human Breast Cancer Cell Lines. Int J Oncol 14 739... [Pg.412]

Several reports have described the anticancer activity of curcumin in a variety of cancer cell lines. In vitro studies have established the activity for curcumin against breast, gastric, hepatic, pancreatic, colorectal, urinary bladder, kidney, prostate, cervical, ovarian, uterine, lung, oral, thymic, and skin cancers. Besides these cancer types, curcumin has shown in vitro therapeutic efficacy against hematological cancers including leukemia, lymphoma, and multiple myeloma. One of our early studies established that the antiproliferative effect of curcumin in human breast cancer cell lines, including hormone-dependent, hormone-independent,... [Pg.364]


See other pages where Human breast cancer cell lines is mentioned: [Pg.17]    [Pg.96]    [Pg.171]    [Pg.336]    [Pg.339]    [Pg.93]    [Pg.119]    [Pg.114]    [Pg.15]    [Pg.196]    [Pg.28]    [Pg.33]    [Pg.43]    [Pg.64]    [Pg.746]    [Pg.50]    [Pg.243]    [Pg.186]    [Pg.759]    [Pg.196]    [Pg.366]    [Pg.314]   
See also in sourсe #XX -- [ Pg.2 , Pg.182 ]




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Breast cancer cell lines

Breast cancer cells, human

Breast cancer line

Breast cell lines

Breast cells

Cancer cell lines

Cancer cells, breast

Cancer, human

Human breast

Human breast cancer

Human breast cancer cell line, MCF

Human cancer cell lines

Human cancer cells

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