TY - JOUR
T1 - Nanomicellar-curcumin exerts its therapeutic effects via affecting angiogenesis, apoptosis, and T cells in a mouse model of melanoma lung metastasis
AU - Mardani, Rajab
AU - Hamblin, Michael R.
AU - Taghizadeh, Mohsen
AU - Banafshe, Hamid Reza
AU - Nejati, Majid
AU - Mokhtari, Mojgan
AU - Borran, Sarina
AU - Davoodvandi, Amirhossein
AU - Khan, Haroon
AU - Jaafari, Mahmoud Reza
AU - Mirzaei, Hamed
N1 - Publisher Copyright:
© 2020 Elsevier GmbH
PY - 2020/9
Y1 - 2020/9
N2 - Background: Curcumin is a natural phytochemical polyphenol with significant anti-cancer effects and negligible side effects. In this study, the therapeutic capacity of nanomicellar-curcumin for treating lung metastasis was evaluated in an immunocompetent mouse model of metastatic melanoma. Martials and methods: Two doses of nanomicellar-curcumin (i.e. 10 and 20 μM) were used to induce cytotoxicity in 3 melanoma cell lines. A total of 60 mice were allocated to 20 mice in each of three groups (10 for survival and 10 for assays). Groups were no treatment control, PBS control, nanomicellar-curcumin 20 mg/kg IP 4 times a week, for three weeks). Immunohistochemistry, TUNEL assay, and Western blots were used on lung samples. Results: Nanomicellar-curcumin inhibited the in vitro growth of B16 F10 melanoma cells at 20 μM over 72 h. In vivo, 20 mg/kg nanomicellar-curcumin injected IP, delayed tumor cell growth and significantly extended mouse survival rate. Tumor infiltration of regulatory T cells and angiogenesis were reduced, while IFN-γ and CXCL10 were increased. Conclusion: Nanomicellar-curcumin can inhibit lung metastasis and growing melanoma via activation of apoptosis, activated T cells and inhibition of angiogenesis, tumor growth and regulatory T cells.
AB - Background: Curcumin is a natural phytochemical polyphenol with significant anti-cancer effects and negligible side effects. In this study, the therapeutic capacity of nanomicellar-curcumin for treating lung metastasis was evaluated in an immunocompetent mouse model of metastatic melanoma. Martials and methods: Two doses of nanomicellar-curcumin (i.e. 10 and 20 μM) were used to induce cytotoxicity in 3 melanoma cell lines. A total of 60 mice were allocated to 20 mice in each of three groups (10 for survival and 10 for assays). Groups were no treatment control, PBS control, nanomicellar-curcumin 20 mg/kg IP 4 times a week, for three weeks). Immunohistochemistry, TUNEL assay, and Western blots were used on lung samples. Results: Nanomicellar-curcumin inhibited the in vitro growth of B16 F10 melanoma cells at 20 μM over 72 h. In vivo, 20 mg/kg nanomicellar-curcumin injected IP, delayed tumor cell growth and significantly extended mouse survival rate. Tumor infiltration of regulatory T cells and angiogenesis were reduced, while IFN-γ and CXCL10 were increased. Conclusion: Nanomicellar-curcumin can inhibit lung metastasis and growing melanoma via activation of apoptosis, activated T cells and inhibition of angiogenesis, tumor growth and regulatory T cells.
KW - Angiogenesis
KW - Apoptosis
KW - Lung metastases
KW - Melanoma
KW - Nanomicellar-curcumin
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=85087411263&partnerID=8YFLogxK
U2 - 10.1016/j.prp.2020.153082
DO - 10.1016/j.prp.2020.153082
M3 - Article
C2 - 32825950
AN - SCOPUS:85087411263
SN - 0344-0338
VL - 216
JO - Pathology Research and Practice
JF - Pathology Research and Practice
IS - 9
M1 - 153082
ER -