This study was designed to investigate the mode of action of trabectedin in myelomonocytic leukemia cells by applying systems biology approaches to mine gene expression profiling data and pharmacological assessment of the cellular effects. Significant enrichment was found in regulons of target genes inferred for specific transcription factors, among which MAFB was the most upregulated after treatment and was central in the transcriptional network likely to be relevant for the specific therapeutic effects of trabectedin against myelomonocytic cells. Using the Connectivity Map, similarity among transcriptional signatures elicited by treatment with different compounds was investigated, showing a high degree of similarity between transcriptiona...
Background: Soft tissue sarcomas (STS) are a rare group of solid neoplasm including among others lip...
Chemotherapy-resistant cancer recurrence is a major cause of mortality. In acute myeloid leukemia (A...
Inhibition of bromodomain and extra terminal (BET) protein family members, including BRD4, decreases...
This study was designed to investigate the mode of action of trabectedin in myelomonocytic leukemia ...
Background: Juvenile myelomonocytic leukaemia (JMML) and chronic myelomonocytic leukaemia (CMML) are...
Background: Genomic instability is a feature of multiple myeloma (MM), and impairment in DNA damagin...
Trabectedin, a new antitumor compound originally derived from a marine tunicate, is clinically effec...
SummaryWe have analyzed the DNA binding properties of the antitumor agent trabectedin (ET-743, Yonde...
Ewing’s sarcoma (ES) is the second most common malignant bone tumor of childhood, characterized by t...
<div><p>Trabectedin, a new antitumor compound originally derived from a marine tunicate, is clinical...
Myxoid liposarcoma (MLPS) is a rare soft tissue sarcoma of the mesenchymal cells characterised by th...
Trabectedin, a new antitumor compound originally derived from a marine tunicate, is clinically effec...
We have analyzed the DNA binding properties of the antitumor agent trabectedin (ET-743, Yondelis) an...
Myxoid Liposarcomas (MLS), characterized by the expression of FUS-CHOP fusion gene are clinically ve...
Trabectedin (Yondelis; ET-743) is a potent anticancer drug that binds to DNA by forming a covalent b...
Background: Soft tissue sarcomas (STS) are a rare group of solid neoplasm including among others lip...
Chemotherapy-resistant cancer recurrence is a major cause of mortality. In acute myeloid leukemia (A...
Inhibition of bromodomain and extra terminal (BET) protein family members, including BRD4, decreases...
This study was designed to investigate the mode of action of trabectedin in myelomonocytic leukemia ...
Background: Juvenile myelomonocytic leukaemia (JMML) and chronic myelomonocytic leukaemia (CMML) are...
Background: Genomic instability is a feature of multiple myeloma (MM), and impairment in DNA damagin...
Trabectedin, a new antitumor compound originally derived from a marine tunicate, is clinically effec...
SummaryWe have analyzed the DNA binding properties of the antitumor agent trabectedin (ET-743, Yonde...
Ewing’s sarcoma (ES) is the second most common malignant bone tumor of childhood, characterized by t...
<div><p>Trabectedin, a new antitumor compound originally derived from a marine tunicate, is clinical...
Myxoid liposarcoma (MLPS) is a rare soft tissue sarcoma of the mesenchymal cells characterised by th...
Trabectedin, a new antitumor compound originally derived from a marine tunicate, is clinically effec...
We have analyzed the DNA binding properties of the antitumor agent trabectedin (ET-743, Yondelis) an...
Myxoid Liposarcomas (MLS), characterized by the expression of FUS-CHOP fusion gene are clinically ve...
Trabectedin (Yondelis; ET-743) is a potent anticancer drug that binds to DNA by forming a covalent b...
Background: Soft tissue sarcomas (STS) are a rare group of solid neoplasm including among others lip...
Chemotherapy-resistant cancer recurrence is a major cause of mortality. In acute myeloid leukemia (A...
Inhibition of bromodomain and extra terminal (BET) protein family members, including BRD4, decreases...