Journal of Enzyme Inhibition and Medicinal Chemistry (Jan 2021)

Exploration of novel heterofused 1,2,4-triazine derivative in colorectal cancer

  • Justyna Magdalena Hermanowicz,
  • Anna Szymanowska,
  • Beata Sieklucka,
  • Robert Czarnomysy,
  • Krystyna Pawlak,
  • Anna Bielawska,
  • Krzysztof Bielawski,
  • Joanna Kalafut,
  • Alicja Przybyszewska,
  • Arkadiusz Surazynski,
  • Adolfo Rivero-Muller,
  • Mariusz Mojzych,
  • Dariusz Pawlak

DOI
https://doi.org/10.1080/14756366.2021.1879803
Journal volume & issue
Vol. 36, no. 1
pp. 535 – 548

Abstract

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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.

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