CIGB-552 is a cell-penetrating peptide that exerts in vitro and in vivo antitumor effect on cancer cells. In the present work, the mechanism involved in such anticancer activity was studied using chemical proteomics and expression-based proteomics in culture cancer cell lines. CIGB-552 interacts with at least 55 proteins, as determined by chemical proteomics. A temporal differential proteomics based on iTRAQ quantification method was performed to identify CIGB-552 modulated proteins. The proteomic profile includes 72 differentially expressed proteins in response to CIGB-552 treatment. Proteins related to cell proliferation and apoptosis were identified by both approaches. In line with previous findings, proteomic data revealed that CIGB-552...
Protein kinase CK2 has emerged as an attractive therapeutic target in acute myeloid leukemia (AML), ...
Abstract Background Lung cancer is the most frequently diagnosed cancer and the leading cause of can...
<p>Pancreatic cancer is characterized by mutated signaling pathways and a high incidence of drug res...
CIGB-552 is a second generation antitumor peptide that displays potent cytotoxicity in lung and colo...
AbstractCIGB-552 is a second generation antitumor peptide that displays potent cytotoxicity in lung ...
Because of resistance development by cancer cells against current anticancer drugs, there is a consi...
Accumulation of the COMMD1 protein as a druggable pharmacology event to target cancer cells has not ...
New selective, efficacious chemotherapy agents are in demand as traditional drugs display side effec...
Despite significant progress in the development of anti-cancer drugs, there is still a need for nove...
CIGB-552 is a twenty-amino-acid novel synthetic peptide that has proven to be effective in reducing ...
Epidermal growth factor receptor (EGFR) is usually overexpressed in nasopharyngeal carcinoma (NPC). ...
CIGB-300 is a cyclic synthetic peptide that induces apoptosis in malignant cells, elicits antitumor ...
Proteomics is becoming increasingly important for cancer biotherapy. The development of high-throug...
Drug induced cell differentiation represents a promising experimental model for proteomic analysis o...
SummaryThe NCI-60 cell line collection is a very widely used panel for the study of cellular mechani...
Protein kinase CK2 has emerged as an attractive therapeutic target in acute myeloid leukemia (AML), ...
Abstract Background Lung cancer is the most frequently diagnosed cancer and the leading cause of can...
<p>Pancreatic cancer is characterized by mutated signaling pathways and a high incidence of drug res...
CIGB-552 is a second generation antitumor peptide that displays potent cytotoxicity in lung and colo...
AbstractCIGB-552 is a second generation antitumor peptide that displays potent cytotoxicity in lung ...
Because of resistance development by cancer cells against current anticancer drugs, there is a consi...
Accumulation of the COMMD1 protein as a druggable pharmacology event to target cancer cells has not ...
New selective, efficacious chemotherapy agents are in demand as traditional drugs display side effec...
Despite significant progress in the development of anti-cancer drugs, there is still a need for nove...
CIGB-552 is a twenty-amino-acid novel synthetic peptide that has proven to be effective in reducing ...
Epidermal growth factor receptor (EGFR) is usually overexpressed in nasopharyngeal carcinoma (NPC). ...
CIGB-300 is a cyclic synthetic peptide that induces apoptosis in malignant cells, elicits antitumor ...
Proteomics is becoming increasingly important for cancer biotherapy. The development of high-throug...
Drug induced cell differentiation represents a promising experimental model for proteomic analysis o...
SummaryThe NCI-60 cell line collection is a very widely used panel for the study of cellular mechani...
Protein kinase CK2 has emerged as an attractive therapeutic target in acute myeloid leukemia (AML), ...
Abstract Background Lung cancer is the most frequently diagnosed cancer and the leading cause of can...
<p>Pancreatic cancer is characterized by mutated signaling pathways and a high incidence of drug res...