4.3 Article

Cancer Spheroid Proliferation Is Suppressed by a Novel Low-toxicity Compound, Pyra-Metho-Carnil, in a Context-independent Manner

Journal

ANTICANCER RESEARCH
Volume 42, Issue 8, Pages 3993-4001

Publisher

INT INST ANTICANCER RESEARCH
DOI: 10.21873/anticanres.15895

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Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan [15K06847, 18K07215, 21K07161, 22K07221]
  2. Fukuoka Foundation for Sound Health Cancer Research Fund

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The study discovered that NPD10621 and its derivatives can selectively suppress the growth of cancer spheroids with mutant KRAS. Among these derivatives, PMC showed the most effective inhibition of mutant KRAS spheroid growth with the least toxicity. Furthermore, PMC was able to suppress the growth of various cancer cell lines, indicating its context-independent role in cancer growth.
Background/Aim: In a screen of compounds to selectively suppress the growth of cancer spheroids, which contained mutant (mt) KRAS, NPD10621 was discovered and associated derivatives were investigated. Materials and Methods: Spheroid areas from HCT116-derived HKe3 spheroids expressing wild type (wt) KRAS (HKe3-wtKRAS) and mtKRAS (HKe3-mtKRAS) were treated with 12 NPD10621 derivatives and measured in three-dimensional floating (3DF) cultures. Several cancers were treated with NPD1018 (pyra-metho-carnil: PMC) in 3DF cultures. In a nude mouse assay, 50% cell growth inhibition (GI50) values were determined. Results: From these 12 derivatives, PMC was the most effective inhibitor of HKe3-mtKRAS spheroid growth with the least toxicity. Furthermore, PMC-mediated growth suppression was observed in all tested cancer cell lines, independent of tissue context, driver gene mutations, and drug resistance, suggesting that the PMC target(s) was crucial for cancer growth in a context-independent manner. The GI50 value of PMC in nude mice assay was 7.7 mg/kg

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