<p><b>Effects on cell cycle of doxorubicin (DX), cisplatin (CDDP) and roscovitine (ROS)</b>, used either alone or in combination, in the human osteosarcoma cell lines U-2OS and Saos-2 and their variants resistant to DX or CDDP. Cell cycle phase distribution was determined by flow cytometry after bromodeoxyuridine (BrdU) incorporation and propidium iodide counterstaining. The intensity of propidium iodide fluorescence (representative for the DNA content) was plotted on the X axis. The intensity of the incorporated BrdU fluorescence (representative for the DNA synthesis) was plotted on the Y axis. Legend: CTR, control cells cultured in drug-free medium; DX, CDDP, ROS, cells treated with their respective IC50 dosages of each drug for 24 h (DX ...
BACKGROUND: Time-dependence of cisplatin (CDDP) and oxaliplatin (L-OHP) cytotoxic effects in A431 a...
The specificity and the temporal location of cell cycle arrest induced by the cyclin-dependent kinas...
Targeting the cell cycle is an attractive anticancer strategy, as its dysregulation is a common, if ...
<p><b>Dose-response curves for roscovitine on U-2OS (A) and Saos-2 (B) osteosarcoma cell lines.</b> ...
<div><p>Cyclin-dependent kinase 2 (CDK2) has been reported to be essential for cell proliferation in...
Cyclin-dependent kinase 2 (CDK2) has been reported to be essential for cell proliferation in several...
<p><b>CDK2 gene and protein knock-down after siRNA transfection</b> in U-2OS (A) and Saos-2 (B) huma...
<p>Drug-sensitive (U-2OS and Saos-2) and resistant (U-2OS/DX580, Saos-2/DX580, U-2OS/CDDP4g and Saos...
The use of CDK2 inhibitors, such as Roscovitine (ROSCO),appears as a therapeutic alternative to over...
PURPOSE: Treatment of tumor cells by chemotherapy activates a series of responses ranging from apopt...
Cyclin-dependent kinases (cdk) play an essential role in the intracellular control of the cell divis...
International audienceDoxorubicin is a genotoxic chemotherapy agent used in treatment of a wide vari...
<p>(A) Cell cycle analysis: the blue area represents the control cells, the red line indicates treat...
The cyclin-dependent kinase (CDK) inhibitor roscovitine is under evaluation in clinical trials for i...
Despite improvements in treatment regimens for osteosarcoma (OS) patients, survival rate has not inc...
BACKGROUND: Time-dependence of cisplatin (CDDP) and oxaliplatin (L-OHP) cytotoxic effects in A431 a...
The specificity and the temporal location of cell cycle arrest induced by the cyclin-dependent kinas...
Targeting the cell cycle is an attractive anticancer strategy, as its dysregulation is a common, if ...
<p><b>Dose-response curves for roscovitine on U-2OS (A) and Saos-2 (B) osteosarcoma cell lines.</b> ...
<div><p>Cyclin-dependent kinase 2 (CDK2) has been reported to be essential for cell proliferation in...
Cyclin-dependent kinase 2 (CDK2) has been reported to be essential for cell proliferation in several...
<p><b>CDK2 gene and protein knock-down after siRNA transfection</b> in U-2OS (A) and Saos-2 (B) huma...
<p>Drug-sensitive (U-2OS and Saos-2) and resistant (U-2OS/DX580, Saos-2/DX580, U-2OS/CDDP4g and Saos...
The use of CDK2 inhibitors, such as Roscovitine (ROSCO),appears as a therapeutic alternative to over...
PURPOSE: Treatment of tumor cells by chemotherapy activates a series of responses ranging from apopt...
Cyclin-dependent kinases (cdk) play an essential role in the intracellular control of the cell divis...
International audienceDoxorubicin is a genotoxic chemotherapy agent used in treatment of a wide vari...
<p>(A) Cell cycle analysis: the blue area represents the control cells, the red line indicates treat...
The cyclin-dependent kinase (CDK) inhibitor roscovitine is under evaluation in clinical trials for i...
Despite improvements in treatment regimens for osteosarcoma (OS) patients, survival rate has not inc...
BACKGROUND: Time-dependence of cisplatin (CDDP) and oxaliplatin (L-OHP) cytotoxic effects in A431 a...
The specificity and the temporal location of cell cycle arrest induced by the cyclin-dependent kinas...
Targeting the cell cycle is an attractive anticancer strategy, as its dysregulation is a common, if ...