| Literature DB >> 33522320 |
Justyna Magdalena Hermanowicz1,2, Anna Szymanowska3, Beata Sieklucka1, Robert Czarnomysy4, Krystyna Pawlak5, Anna Bielawska3, Krzysztof Bielawski4, Joanna Kalafut6, Alicja Przybyszewska6, Arkadiusz Surazynski7, Adolfo Rivero-Muller6, Mariusz Mojzych8, Dariusz Pawlak1,9.
Abstract
Colorectal cancer (CRC) is the third leading cause of cancer-related deaths in men and in women. The impact of the new pyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine sulphonamide (MM-129) was evaluated against human colon cancer in vitro and in zebrafish xenografts. Our results show that this new synthesised compound effectively inhibits cell survival in BTK-dependent mechanism. Its effectiveness is much higher at a relatively low concentration as compared with the standard chemotherapy used for CRC, i.e. 5-fluorouracil (5-FU). Flow cytometry analysis after annexin V-FITC and propidium iodide staining revealed that apoptosis was the main response of CRC cells to MM-129 treatment. We also found that MM-129 effectively inhibits tumour development in zebrafish embryo xenograft model, where it showed a markedly synergistic anticancer effect when used in combination with 5-FU. The above results suggest that this novel heterofused 1,2,4-triazine derivative may be a promising candidate for further evaluation as chemotherapeutic agent against CRC.Entities:
Keywords: 1,2,4-Triazine derivative; apoptosis; colon cancer; zebrafish
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Year: 2021 PMID: 33522320 PMCID: PMC7850456 DOI: 10.1080/14756366.2021.1879803
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051