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Marko Klobučar

Researcher at University of Rijeka

Publications -  19
Citations -  252

Marko Klobučar is an academic researcher from University of Rijeka. The author has contributed to research in topics: Cancer & Colorectal cancer. The author has an hindex of 8, co-authored 18 publications receiving 179 citations.

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Novel Coumarin Derivatives Containing 1,2,4-Triazole, 4,5-Dicyanoimidazole and Purine Moieties: Synthesis and Evaluation of Their Cytostatic Activity

TL;DR: Results of anti-proliferative assays performed on a panel of selected human tumor cell lines revealed that compound 6 had moderate cytostatic activity against the HeLa cell line, whereas compound 10 showed moderate activity againstthe HeLa, HepG2 and SW620 cell lines.
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Green synthesis and biological evaluation of 6-substituted-2-(2-hydroxy/methoxy phenyl)benzothiazole derivatives as potential antioxidant, antibacterial and antitumor agents.

TL;DR: Several novel 6-substituted-2-arylbenzothiazole compounds were revealed, with strong and selective antiproliferative activity towards HeLa cells in micro and submicromolar concentrations, with the most selective compounds being 6-ammonium-2-(2-hydroxy/methoxyphenyl)benZothiazoles 5f and 6f.
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Basement membrane protein ladinin-1 and the MIF-CD44-β1 integrin signaling axis are implicated in laryngeal cancer metastasis.

TL;DR: In this paper, the authors performed quantitative proteomic profiling of patient-matched primary tumor and adjacent non-tumorous tissues derived from metastatic laryngeal squamous cell carcinoma (LSCC) to identify new protein candidates with potential diagnostic and therapeutic significance.
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Antitumor and antiviral activities of 4-substituted 1,2,3-triazolyl-2,3-dibenzyl-L-ascorbic acid derivatives.

TL;DR: Analysis showed that compound 8m strongly enhanced expression of hypoxia inducible transcription factor 1 α and to some extent decreased expression of nitric oxide synthase 2 (NOS2) suggesting its role in regulating HIF-1α signalling pathway.
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Dual sphingosine kinase inhibitor SKI-II enhances sensitivity to 5-fluorouracil in hepatocellular carcinoma cells via suppression of osteopontin and FAK/IGF-1R signalling

TL;DR: Investigation of the anticancer efficacy and underlying molecular mechanisms of combined administration of 5-FU and dual Sphk1/Sphk2 inhibitor SKI-II in HepG2 hepatocellular carcinoma cells show that pharmacological blockade of both Sphk isoforms represents a promising strategy to boost the anti-tumour efficacy of5-FU.