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Synergistic interactions of the anti-casein kinase 2 CIGB-300 peptide and chemotherapeutic agents in lung and cervical preclinical cancer models.
TLDR
Findings provide a rationale for combining the anti-CK2 CIGB-300 peptide with currently available anticancer agents in the clinical setting and indicate platins and taxanes as compounds with major perspectives. Expand
CIGB-300, a novel proapoptotic peptide that impairs the CK2 phosphorylation and exhibits anticancer properties both in vitro and in vivo
TLDR
These results provide an early proof-of-principle of clinical benefit by using an anti-CK2 approach in cancer and are the first clinical trial where an investigational drug has been used to target the CK2 phosphorylation domain. Expand
Human papillomavirus type 16 E7 impairs the activation of the interferon regulatory factor-1.
TLDR
The data indicate that HPV-16 E7 inhibits the IRF-1 and NFkappaB function and this could lead to the impairment of the IFN response in HPV-infected cells and the findings suggest that different events of theIFN inducible signal cascade seem to be target for HPV- 16 E7. Expand
Detection and typing of human papillomavirus DNA in benign and malignant tumours of laryngeal epithelium.
TLDR
HPV 16 was the type most frequently found in laryngeal carcinoma samples and this results support an etiologic role for this type of HPV in the pathogenesis of larynx carcinoma. Expand
Obtaining Biologically Active IL-15 in Escherichia coli ; Obtención de IL-15 Biológicamente Activa en Escherichia coli
Interleukin-15 (IL-15) is a recently discovered cytokine that shares with interleukin-2 (IL-2) the beta and gamma subunits of the receptor complex, therefore, both of them display similar biologicalExpand
Differential expression of the p27Kip1 mRNA in IFN-sensitive and resistant cell lines.
TLDR
The results suggest that p27Kip1 could be a key mediator of the IFN alpha 2b-induced growth arrest and that HPV 16 E7 might affect p27 kip1 inducibility, originating IFNalpha 2B-resistant cells. Expand
Anticancer peptide CIGB-300 binds to nucleophosmin/B23, impairs its CK2-mediated phosphorylation, and leads to apoptosis through its nucleolar disassembly activity
TLDR
Findings provide important clues by which the CIGB-300 peptide exerts its proapoptotic effect on tumor cells and highlights the suitability of the B23/CK2 pathway for cancer-targeted therapy. Expand
Mechanisms of cellular uptake, intracellular transportation, and degradation of CIGB-300, a Tat-conjugated peptide, in tumor cell lines.
TLDR
This work studied differential antiproliferative behavior in terms of cellular uptake, intracellular transportation, and degradation in tumor cell lines with dissimilar sensitivity to CIGB-300 to suggest a mechanism of internalization, vesicular transportation, but also suggests degradation in highly sensitive cells. Expand
CIGB-300: A peptide-based drug that impairs the Protein Kinase CK2-mediated phosphorylation.
TLDR
The clinical data demonstrate the safety, tolerability, and clinical effects of intratumoral injections of CIGB-300 and provide the foundation for future phase 3 clinical trials in locally advanced cervical cancer in combination with standard chemoradiotherapy. Expand
Treatment with an Anti-CK2 Synthetic Peptide Improves Clinical Response in Covid-19 Patients with Pneumonia. A Randomized and Controlled Clinical Trial
TLDR
This first report describing signs of clinical benefit of an anti-CK2 approach in Covid-19 is described, revealing that consecutive-5 day regimen of intravenous CIGB-325 at 2.5 mg/kg quickly improved the chest-CT outcomes over standard-of-care. Expand
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