CCL

Összesen 2 találat.
#/oldal:
Részletezés:
Rendezés:

1.

001-es BibID:BIBFORM005088
Első szerző:Krasznai Zoárd Tibor (szülész-nőgyógyász, gyermeknőgyógyász)
Cím:Paclitaxel modifies the accumulation of tumor-diagnostic tracers in different ways in P-glycoprotein-positive and negative cancer cells / Krasznai, Z. T., Peli-Szabo, J., Nemeth, E., Balkay, L., Szabo, G., Goda, K., Galuska, L., Tron, L., Major, T., Hernadi, Z.
Dátum:2006
ISSN:928-0987 (Print)
Megjegyzések:To study how paclitaxel treatment modifies the accumulation of tumor-diagnostic radiotracers in P-glycoprotein (P-gp) positive and negative cancer cells. METHODS: The accumulations of different P-gp substrates, including rhodamine 123, daunorubicin and [(99m)Tc]hexakis-2-methoxybutyl isonitrile ((99m)Tc-MIBI), were measured in P-gp-positive (A2780AD) and P-gp-negative human ovarian carcinoma cells (A2780) and JY human lymphoid B cells. The uptakes of the tumor-diagnostic tracers (11)C-choline and 2-[(18)F]fluoro-2-deoxy-d-glucose ((18)FDG) were measured in the same cell lines. The P-gp expression and function were demonstrated by flow-cytometry. RESULTS: The (18)FDG measurements revealed that the glucose metabolic rate was significantly higher (p<0.01) in the P-gp-positive A2780AD cells than in the P-gp-negative cells. Paclitaxel (1-70microM) increased the (18)FDG uptake (up to 200%) of both P-gp-positive and P-gp-negative cells, whereas it did not modulate their (11)C-choline uptake. Paclitaxel reinstated the (99m)Tc-MIBI accumulation of the A2780AD cells (to 1500% of the control) in a concentration-dependent manner, while it increased the uptake of the P-gp-negative cells to a lesser extent (to a maximum of 200% of the control). CONCLUSION: Paclitaxel modifies the uptake of tumor-diagnostic tracers in both P-gp-dependent and independent manners. Interpretation of the multifactorial effects of paclitaxel may promote a correct in vivo diagnosis of P-gp-positive and P-gp-negative tumors.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Antineoplastic Agents
Antineoplastic Agents,Phytogenic
Binding Sites
Biological Transport
Carcinoma
Cell Line
Cell Line,Tumor
Cells
Comparative Study
Daunorubicin
diagnosis
Drug Resistance,Neoplasm
Flow Cytometry
Fluorodeoxyglucose F18
Glucose
Human
Humans
Hungary
Kinetics
metabolism
methods
P-Glycoprotein
Paclitaxel
Protein Binding
Radioactive Tracers
Radiopharmaceuticals
Rhodamine 123
Technetium Tc 99m Sestamibi
Megjelenés:European Journal of Pharmaceutical Sciences. - 28 : 3 (2006), p. 249-256. -
További szerzők:Péli-Szabó Judit (1977-) (vegyész) Németh Enikő (1977-) (vegyész) Balkay László (1963-) (biofizikus) Szabó Gábor (1953-) (biofizikus) Goda Katalin (1969-) (biofizikus) Galuska László (1946-) (belgyógyász, izotópdiagnoszta) Trón Lajos (1941-) (biofizikus) Major Tamás (1963-) (szülész-nőgyógyász) Hernádi Zoltán (1948-) (szülész-nőgyógyász, klinikai onkológus)
Internet cím:elektronikus változat
DOI
Borító:

2.

001-es BibID:BIBFORM004874
035-os BibID:(scopus)21144454228 (wos)000229662400002
Első szerző:Márián Teréz (radiobiológus)
Cím:Biphasic accumulation kinetics of [99mTc]-hexakis-2-methoxyisobutyl isonitrile in tumour cells and its modulation by lipophilic P-glycoprotein ligands / Marian, T., Balkay, L., Szabo, G., Krasznai, Z. T., Hernadi, Z., Galuska, L., Szabo-Peli, J., Esik, O., Tron, L., Krasznai, Z.
Dátum:2005
ISSN:0928-0987
Megjegyzések:To study the accumulation and washout kinetics of [99mTc]-hexakis-2-methoxyisobutyl isonitrile (99mTc-MIBI) in MDR positive and MDR negative tumour cells and how this is modified by lipophilic P-glycoprotein ligands. METHODS: The tumour cells were incubated in the presence and absence of the ligands and the uptakes of 99mTc-MIBI, rhodamine 123 and 2-[18F]fluoro-2-deoxy-D-glucose (18FDG) were measured. RESULTS: The accumulation of 99mTc-MIBI in the tumour cells followed biphasic kinetics. Verapamil and cyclosporin A increased the membrane fluidity and significantly enhanced the 99mTc-MIBI uptake of the MDR negative cells, while the rhodamine 123 uptake was not affected. Verapamil significantly increased the uptake of rhodamine 123 and 18FDG but did not modify that of 99mTc-MIBI in the MDR positive cells. Cyclosporin A significantly increased the 18FDG uptake of the MDR positive and negative tumour cells; these effects were ouabain-sensitive. Depolarization of the cytoplasmic membrane, acidification of the extracellular medium and the administration of CCCP decreased the accumulation of 99mTc-MIBI and rhodamine 123 uptake in the tumour cells. CONCLUSIONS: Lipophilic P-glycoprotein ligands modified the biphasic accumulation kinetics of the 99mTc-MIBI uptakes of MDR negative and positive tumour cells in different and complex ways and could therefore mask the P-glycoprotein pump-dependent changes in tracer accumulation.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Animals
Cell Line,Tumor
Cells
Cricetinae
Cyclosporine
drug effects
Drug Resistance,Multiple
Fluorine
Fluorine Radioisotopes
Gluconates
Humans
Hungary
Intracellular Membranes
Kinetics
Ligands
Membrane Fluidity
Membrane Potentials
metabolism
methods
Mice
Mitochondria
P-Glycoprotein
Permeability
pharmacokinetics
pharmacology
physiology
Radioisotopes
Research
Rhodamine 123
Support
Technetium Tc 99m Sestamibi
Verapamil
Megjelenés:European Journal of Pharmaceutical Sciences. - 25 : 2-3 (2005), p. 201-209. -
További szerzők:Balkay László (1963-) (biofizikus) Szabó Gábor (1953-) (biofizikus) Krasznai Zoárd Tibor (1973-) (szülész-nőgyógyász, gyermeknőgyógyász) Hernádi Zoltán (1948-) (szülész-nőgyógyász, klinikai onkológus) Galuska László (1946-) (belgyógyász, izotópdiagnoszta) Szabó-Péli Judit (1977-) (kutató) Ésik Olga Trón Lajos (1941-) (biofizikus) Krasznai Zoltán (1950-) (biofizikus)
Internet cím:elektronikus változat
DOI
Borító:
Rekordok letöltése1