Although medicinal mushroom extracts have been proposed as promising anti-cancer agents, their precise impacts on metastatic breast cancer are still to be clarified. For this purpose, the present study exploited the effect of a novel medicinal mushroom blend, namely Micotherapy U-care, in a 4T1 triple-negative mouse breast cancer model. Mice were orally administered with Micotherapy U-care, consisting of a mixture of Agaricus blazei, Ophiocordyceps sinensis, Ganoderma lucidum, Grifola frondosa, and Lentinula edodes. The syngeneic tumor-bearing mice were generated by injecting 4T1 cells in both supplemented and non-supplemented mice. After sacrifice 25 days later, specific endpoints and pathological outcomes of the murine pulmonary tissue were evaluated. (i) Histopathological and ultrastructural analysis and (ii) immunohistochemical assessment of TGF-ß1, IL-6 and NOS2, COX2, SOD1 as markers of inflammation and oxidative stress were performed. The QoL was comparatively evaluated. Micotherapy U-care supplementation, starting before 4T1 injection and lasting until the end of the experiment, dramatically reduced the pulmonary metastases density, also triggering a decrease of fibrotic response, and reducing IL-6, NOS, and COX2 expression. SOD1 and TGF-ß1 results were also discussed. These findings support the valuable potential of Micotherapy U-care as adjuvant therapy in the critical management of triple-negative breast cancer.

Novel medicinal mushroom blend as a promising supplement in integrative oncology : A multi-tiered study using 4t1 triple-negative mouse breast cancer model / E. Roda, F. De Luca, C. Di Iorio, D. Ratto, S. Siciliani, B. Ferrari, F. Cobelli, G. Borsci, E.C. Priori, S. Chinosi, A. Ronchi, R. Franco, R. Di Francia, M. Berretta, C.A. Locatelli, A. Gregori, E. Savino, M.G. Bottone, P. Rossi. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1661-6596. - 21:10(2020), pp. 3479.1-3479.28. [10.3390/ijms21103479]

Novel medicinal mushroom blend as a promising supplement in integrative oncology : A multi-tiered study using 4t1 triple-negative mouse breast cancer model

E.C. Priori;
2020

Abstract

Although medicinal mushroom extracts have been proposed as promising anti-cancer agents, their precise impacts on metastatic breast cancer are still to be clarified. For this purpose, the present study exploited the effect of a novel medicinal mushroom blend, namely Micotherapy U-care, in a 4T1 triple-negative mouse breast cancer model. Mice were orally administered with Micotherapy U-care, consisting of a mixture of Agaricus blazei, Ophiocordyceps sinensis, Ganoderma lucidum, Grifola frondosa, and Lentinula edodes. The syngeneic tumor-bearing mice were generated by injecting 4T1 cells in both supplemented and non-supplemented mice. After sacrifice 25 days later, specific endpoints and pathological outcomes of the murine pulmonary tissue were evaluated. (i) Histopathological and ultrastructural analysis and (ii) immunohistochemical assessment of TGF-ß1, IL-6 and NOS2, COX2, SOD1 as markers of inflammation and oxidative stress were performed. The QoL was comparatively evaluated. Micotherapy U-care supplementation, starting before 4T1 injection and lasting until the end of the experiment, dramatically reduced the pulmonary metastases density, also triggering a decrease of fibrotic response, and reducing IL-6, NOS, and COX2 expression. SOD1 and TGF-ß1 results were also discussed. These findings support the valuable potential of Micotherapy U-care as adjuvant therapy in the critical management of triple-negative breast cancer.
Agaricus blazei; Breast cancer; Complementary medicine; Ganoderma lucidum; Grifola frondosa; In vivo; Lentinula edodes; Lung metastasis; Mycotherapy; Ophiocordyceps sinensis; Agaricales; Animals; Cell Line, Tumor; Cell Proliferation; Dietary Supplements; Disease Models, Animal; Female; Humans; Mice; Plants, Medicinal; Triple Negative Breast Neoplasms; Integrative Oncology
Settore BIO/06 - Anatomia Comparata e Citologia
Settore BIO/09 - Fisiologia
2020
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/902301
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