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STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells

Signal transducer and activator of transcription 3 (STAT3) signalling serves an important role in carcinogenesis and cellular senescence, and its inhibition in tumour cells represents an attractive therapeutic target. Premature cellular senescence, a process of permanent proliferative arrest of cell...

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Autores principales: Mikyskova, Romana, Sapega, Olena, Psotka, Miroslav, Novotny, Ondrej, Hodny, Zdeněk, Balintova, Sona, Malinak, David, Svobodova, Jana, Andrys, Rudolf, Rysanek, David, Musilek, Kamil, Reinis, Milan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018236/
https://www.ncbi.nlm.nih.gov/pubmed/36825563
http://dx.doi.org/10.3892/mmr.2023.12968
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author Mikyskova, Romana
Sapega, Olena
Psotka, Miroslav
Novotny, Ondrej
Hodny, Zdeněk
Balintova, Sona
Malinak, David
Svobodova, Jana
Andrys, Rudolf
Rysanek, David
Musilek, Kamil
Reinis, Milan
author_facet Mikyskova, Romana
Sapega, Olena
Psotka, Miroslav
Novotny, Ondrej
Hodny, Zdeněk
Balintova, Sona
Malinak, David
Svobodova, Jana
Andrys, Rudolf
Rysanek, David
Musilek, Kamil
Reinis, Milan
author_sort Mikyskova, Romana
collection PubMed
description Signal transducer and activator of transcription 3 (STAT3) signalling serves an important role in carcinogenesis and cellular senescence, and its inhibition in tumour cells represents an attractive therapeutic target. Premature cellular senescence, a process of permanent proliferative arrest of cells in response to various inducers, such as cytostatic drugs or ionizing radiation, is accompanied by morphological and secretory changes, and by altered susceptibility to chemotherapeutic agents, which can thereby complicate their eradication by cancer therapies. In the present study, the responsiveness of proliferating and docetaxel (DTX)-induced senescent cancer cells to small molecule STAT3 inhibitor Stattic and its analogues was evaluated using tumour cell lines. These agents displayed cytotoxic effects in cell viability assays on both proliferating and senescent murine TRAMP-C2 and TC-1 cells; however, senescent cells were markedly more resistant. Western blot analysis revealed that Stattic and its analogues effectively inhibited constitutive STAT3 phosphorylation in both proliferating and senescent cells. Furthermore, whether the Stattic-derived inhibitor K1836 could affect senescence induction or modulate the phenotype of senescent cells was evaluated. K1836 treatment demonstrated no effect on senescence induction by DTX. However, the K1836 compound significantly modulated secretion of certain cytokines (interleukin-6, growth-regulated oncogene α and monocyte chemoattractant protein-1). In summary, the present study demonstrated differences between proliferating and senescent tumour cells in terms of their susceptibility to STAT3 inhibitors and demonstrated the ability of the new STAT3 inhibitor K1836 to affect the secretion of essential components of the senescence-associated secretory phenotype. The present study may be useful for further development of STAT3 inhibitor-based therapy of cancer or age-related diseases.
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spelling pubmed-100182362023-03-17 STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells Mikyskova, Romana Sapega, Olena Psotka, Miroslav Novotny, Ondrej Hodny, Zdeněk Balintova, Sona Malinak, David Svobodova, Jana Andrys, Rudolf Rysanek, David Musilek, Kamil Reinis, Milan Mol Med Rep Articles Signal transducer and activator of transcription 3 (STAT3) signalling serves an important role in carcinogenesis and cellular senescence, and its inhibition in tumour cells represents an attractive therapeutic target. Premature cellular senescence, a process of permanent proliferative arrest of cells in response to various inducers, such as cytostatic drugs or ionizing radiation, is accompanied by morphological and secretory changes, and by altered susceptibility to chemotherapeutic agents, which can thereby complicate their eradication by cancer therapies. In the present study, the responsiveness of proliferating and docetaxel (DTX)-induced senescent cancer cells to small molecule STAT3 inhibitor Stattic and its analogues was evaluated using tumour cell lines. These agents displayed cytotoxic effects in cell viability assays on both proliferating and senescent murine TRAMP-C2 and TC-1 cells; however, senescent cells were markedly more resistant. Western blot analysis revealed that Stattic and its analogues effectively inhibited constitutive STAT3 phosphorylation in both proliferating and senescent cells. Furthermore, whether the Stattic-derived inhibitor K1836 could affect senescence induction or modulate the phenotype of senescent cells was evaluated. K1836 treatment demonstrated no effect on senescence induction by DTX. However, the K1836 compound significantly modulated secretion of certain cytokines (interleukin-6, growth-regulated oncogene α and monocyte chemoattractant protein-1). In summary, the present study demonstrated differences between proliferating and senescent tumour cells in terms of their susceptibility to STAT3 inhibitors and demonstrated the ability of the new STAT3 inhibitor K1836 to affect the secretion of essential components of the senescence-associated secretory phenotype. The present study may be useful for further development of STAT3 inhibitor-based therapy of cancer or age-related diseases. D.A. Spandidos 2023-02-22 /pmc/articles/PMC10018236/ /pubmed/36825563 http://dx.doi.org/10.3892/mmr.2023.12968 Text en Copyright: © Mikyskova et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Mikyskova, Romana
Sapega, Olena
Psotka, Miroslav
Novotny, Ondrej
Hodny, Zdeněk
Balintova, Sona
Malinak, David
Svobodova, Jana
Andrys, Rudolf
Rysanek, David
Musilek, Kamil
Reinis, Milan
STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells
title STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells
title_full STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells
title_fullStr STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells
title_full_unstemmed STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells
title_short STAT3 inhibitor Stattic and its analogues inhibit STAT3 phosphorylation and modulate cytokine secretion in senescent tumour cells
title_sort stat3 inhibitor stattic and its analogues inhibit stat3 phosphorylation and modulate cytokine secretion in senescent tumour cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018236/
https://www.ncbi.nlm.nih.gov/pubmed/36825563
http://dx.doi.org/10.3892/mmr.2023.12968
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