Therapeutic Responses to Two New SN-38 Derivatives in Colorectal Cancer Patient-Derived Xenografts and Respective 3D<i>In Vitro</i>Cultures

The new SN-38 derivatives, BN-MOA and BN-NMe, showed enhanced therapeutic effects compared to irinotecan in CRC models. BN-MOA demonstrated superior tumor inhibition in vivo, while BN-NMe had similar in vitro activity to SN-38. These findings highlight the potential of BN-MOA for greater antitumor efficacy in vivo, with BN-NMe showing comparable effectiveness to SN-38 in vitro. Future studies should optimize growth models to better predict anticancer drug responses.

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Publication Details

Journal
Anticancer Research
Published
2024-09-30
DOI
https://doi.org/10.21873/anticanres.17252
Citations
3
Primary Topic
Colorectal Cancer Treatments and Studies
Type
article
Field-Weighted Citation Impact
0.85
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article

Therapeutic Responses to Two New SN-38 Derivatives in Colorectal Cancer Patient-Derived Xenografts and Respective 3DIn VitroCultures

Justyna Kocik-Krol, Katarzyna Unrug-Bielawska, Jerzy Ostrowski, Krzysztof Klimkiewicz et al.
3 citations
Anticancer Research
Colorectal Cancer Treatments and Studies
0.85
article

Therapeutic Responses to Two New SN-38 Derivatives in Colorectal Cancer Patient-Derived Xenografts and Respective 3DIn VitroCultures

Justyna Kocik-Krol, Katarzyna Unrug-Bielawska, Jerzy Ostrowski, Krzysztof Klimkiewicz, David L. Earnshaw, Magdalena Urbanowicz, Zuzanna Sandowska-Markiewicz, Beata Naumczuk, Michał Mikuła, Marcin Krzykawski, Lech Kozerski, Magdalena Cybulska, Małgorzata Statkiewicz, Izabela Rumieńczyk, Ewelina Kaniuga, Michalina Dąbrowska
article en
3 citations

Abstract

The new SN-38 derivatives, BN-MOA and BN-NMe, showed enhanced therapeutic effects compared to irinotecan in CRC models. BN-MOA demonstrated superior tumor inhibition in vivo, while BN-NMe had similar in vitro activity to SN-38. These findings highlight the potential of BN-MOA for greater antitumor efficacy in vivo, with BN-NMe showing comparable effectiveness to SN-38 in vitro. Future studies should optimize growth models to better predict anticancer drug responses.

Anticancer ResearchVol. 44(10)
Institute of Organic Chemistry (PL), National Institute of Oncology (HU), Postgraduate School of Molecular Medicine (PL), Krakow Cardiovascular Research Institute (PL), The Maria Sklodowska-Curie National Research Institute of Oncology (PL), Narodowy Instytut Leków (PL), Polish Academy of Sciences (PL)
Zero hunger
Openalex Percentile: Top 22%
Colorectal Cancer Treatments and Studies
0.85
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