Background: several experimental findings and epidemiological observations indicated that aspirin/acetylsalicylic acid (ASA) may be endowed with anticancer effects against a variety of human malignancies, including thyroid carcinomas. Among these, undifferentiated/anaplastic thyroid carcinoma (ATC) is one of the most aggressive and lethal human cancers, refractory to all currently available therapies. Methods: we here evaluated in a preclinical setting the effects of ASA on a panel of three ATC-derived cell lines: the CAL-62, the 8305C, and the 8505C. Results: the data obtained demonstrated the ability of ASA to inhibit, in a dose- and time-dependent manner, the proliferation of all ATC cell lines investigated, with IC50 values comprised between 2.0 and 4.3 mM. Cell growth was restrained with the same efficacy when the ASA treatment was applied to three-dimensional soft-agar cultures. In addition, ASA significantly reduced migration and invasion in two of the three ATC cell lines. We finally investigated the effects of ASA on the MAPK and PI3K/Akt signaling pathways, which are often altered in ATC. The results showed that the phosphorylation status of the Akt1/2/3 kinases was significantly reduced following ASA treatment, while ERK1/2 phosphorylation was either unaffected or slightly upregulated. Conclusions: our findings support epidemiological evidence on the anticancer potential of ASA. On this basis, further investigations should be carried out to assess the usefulness of ASA as adjuvant therapy in patients affected by ATC.

The Potential Therapeutic Value of Aspirin in Anaplastic Thyroid Cancer / Baldini, Enke; Cardarelli, Silvia; Lori, Eleonora; Bonati, Elena; Gagliardi, Federica; Pironi, Daniele; Fallahi, Poupak; Antonelli, Alessandro; D'Andrea, Vito; Ulisse, Salvatore; Sorrenti, Salvatore. - In: CANCERS. - ISSN 2072-6694. - 16:24(2024). [10.3390/cancers16244203]

The Potential Therapeutic Value of Aspirin in Anaplastic Thyroid Cancer.

Baldini, Enke;Cardarelli, Silvia;Lori, Eleonora;Gagliardi, Federica;Pironi, Daniele;D'Andrea, Vito;Ulisse, Salvatore
;
Sorrenti, Salvatore
2024

Abstract

Background: several experimental findings and epidemiological observations indicated that aspirin/acetylsalicylic acid (ASA) may be endowed with anticancer effects against a variety of human malignancies, including thyroid carcinomas. Among these, undifferentiated/anaplastic thyroid carcinoma (ATC) is one of the most aggressive and lethal human cancers, refractory to all currently available therapies. Methods: we here evaluated in a preclinical setting the effects of ASA on a panel of three ATC-derived cell lines: the CAL-62, the 8305C, and the 8505C. Results: the data obtained demonstrated the ability of ASA to inhibit, in a dose- and time-dependent manner, the proliferation of all ATC cell lines investigated, with IC50 values comprised between 2.0 and 4.3 mM. Cell growth was restrained with the same efficacy when the ASA treatment was applied to three-dimensional soft-agar cultures. In addition, ASA significantly reduced migration and invasion in two of the three ATC cell lines. We finally investigated the effects of ASA on the MAPK and PI3K/Akt signaling pathways, which are often altered in ATC. The results showed that the phosphorylation status of the Akt1/2/3 kinases was significantly reduced following ASA treatment, while ERK1/2 phosphorylation was either unaffected or slightly upregulated. Conclusions: our findings support epidemiological evidence on the anticancer potential of ASA. On this basis, further investigations should be carried out to assess the usefulness of ASA as adjuvant therapy in patients affected by ATC.
2024
anaplastic thyroid cancer; aspirin; therapy
01 Pubblicazione su rivista::01a Articolo in rivista
The Potential Therapeutic Value of Aspirin in Anaplastic Thyroid Cancer / Baldini, Enke; Cardarelli, Silvia; Lori, Eleonora; Bonati, Elena; Gagliardi, Federica; Pironi, Daniele; Fallahi, Poupak; Antonelli, Alessandro; D'Andrea, Vito; Ulisse, Salvatore; Sorrenti, Salvatore. - In: CANCERS. - ISSN 2072-6694. - 16:24(2024). [10.3390/cancers16244203]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1730494
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