Quercetin enhances transforming growth factor beta 1 secretion by human ovarian cancer cells. 1994

G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
Department of Gynecology, Catholic University, Rome, Italy.

Our study demonstrates that quercetin (Q)-induced growth-inhibitory activity in ovarian cancer cells may be mediated by modulation of transforming growth factor beta 1 (TGF beta 1) production. We used the OVCA 433 cell line which is very sensitive to the anti-proliferative effect of Q and expresses high-affinity, low-capacity TGF beta 1 receptors. Conditioned medium (CM) from Q-treated cells is able to displace 125I-TGF beta 1 from binding to its receptor; moreover Q (10 microM) increases TGF beta 1 activity in CM in a time-dependent fashion starting after 4 hr and reaching a maximum by 24 hr of Q treatment. Q-induced growth inhibition is reversed by a neutralizing anti-TGF beta 1 MAb both in OVCA 433 and in a clonogenic assay of cells from a primary ovarian tumor. Q-induced increase of TGF beta 1 activity in CM is specific since other anti-proliferative compounds, such as Dexamethasone, which is as active on the cell cycle as Q, had no effect on TGF beta 1 secretion. Northern-blot analysis of TGF beta 1 mRNA levels at various times of Q (10 microM) exposure revealed that there was no increase, suggesting that regulation of TGF beta 1 occurs at posttranscriptional levels.

UI MeSH Term Description Entries
D010051 Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. Cancer of Ovary,Ovarian Cancer,Cancer of the Ovary,Neoplasms, Ovarian,Ovary Cancer,Ovary Neoplasms,Cancer, Ovarian,Cancer, Ovary,Cancers, Ovarian,Cancers, Ovary,Neoplasm, Ovarian,Neoplasm, Ovary,Neoplasms, Ovary,Ovarian Cancers,Ovarian Neoplasm,Ovary Cancers,Ovary Neoplasm
D011794 Quercetin A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin. 3,3',4',5,7-Pentahydroxyflavone,Dikvertin
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014407 Tumor Cells, Cultured Cells grown in vitro from neoplastic tissue. If they can be established as a TUMOR CELL LINE, they can be propagated in cell culture indefinitely. Cultured Tumor Cells,Neoplastic Cells, Cultured,Cultured Neoplastic Cells,Cell, Cultured Neoplastic,Cell, Cultured Tumor,Cells, Cultured Neoplastic,Cells, Cultured Tumor,Cultured Neoplastic Cell,Cultured Tumor Cell,Neoplastic Cell, Cultured,Tumor Cell, Cultured
D016212 Transforming Growth Factor beta A factor synthesized in a wide variety of tissues. It acts synergistically with TGF-alpha in inducing phenotypic transformation and can also act as a negative autocrine growth factor. TGF-beta has a potential role in embryonal development, cellular differentiation, hormone secretion, and immune function. TGF-beta is found mostly as homodimer forms of separate gene products TGF-beta1, TGF-beta2 or TGF-beta3. Heterodimers composed of TGF-beta1 and 2 (TGF-beta1.2) or of TGF-beta2 and 3 (TGF-beta2.3) have been isolated. The TGF-beta proteins are synthesized as precursor proteins. Bone-Derived Transforming Growth Factor,Platelet Transforming Growth Factor,TGF-beta,Milk Growth Factor,TGFbeta,Bone Derived Transforming Growth Factor,Factor, Milk Growth,Growth Factor, Milk

Related Publications

G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
September 1992, Immunology,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
July 2000, Cytokine,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
January 1993, Nutrition and cancer,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
July 1995, Neurologia medico-chirurgica,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
December 1992, Biochimica et biophysica acta,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
August 1998, Surgery,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
March 1996, Neurologia medico-chirurgica,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
January 1993, Growth factors (Chur, Switzerland),
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
January 1995, Experimental cell research,
G Scambia, and P B Panici, and F O Ranelletti, and G Ferrandina, and R De Vincenzo, and M Piantelli, and V Masciullo, and G Bonanno, and G Isola, and S Mancuso
July 1994, Cancer,
Copied contents to your clipboard!