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[The therapeutic effect of HSV1-hGM-CSF combined with doxorubicin on the mouse breast cancer model].
Zhuang, X F; Zhang, S R; Liu, B L; Wu, J L; Li, X Q; Gu, H G; Shu, Y.
Afiliación
  • Zhuang XF; Department of Oncology, the Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
  • Zhang SR; Department of Immunology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
  • Liu BL; Key Laboratory of Fermentation Engineer (Ministry of Education), Hubei Provincial Cooperative Innovation Center of Industrial Fermentation, Hubei Key Laboratory of Industrial Microbiology, Hubei University of Technology, Wuhan 430068, China.
  • Wu JL; School of Pharmacology, Hubei University of Science and Technology, Xianning 437100, China.
  • Li XQ; Department of Oncology, the Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
  • Gu HG; Department of Oncology, the Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
  • Shu Y; Department of Central Laboratory, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Zhonghua Zhong Liu Za Zhi ; 40(3): 178-185, 2018 Mar 23.
Article en Zh | MEDLINE | ID: mdl-29575835
ABSTRACT

Objective:

To evaluate the oncolytic effect of herpes simplex virus type 1 which carried recombined human granulocyte-macrophage colony-stimulating factor (HSV1-hGM-CSF) on the mouse breast cancer cell line 4T1 and compare the anticancer effects of HSV1-hGM-CSF, doxorubicin alone or combination on the breast cancer in mice.

Methods:

We investigated the cytotoxic effect on 4T1 cells in vitro, the cell growth, cell apoptosis and cell cycle of 4T1 cells treated with oncolytic HSV1-hGM-CSF at different MOIs (0, 0.5, 1 and 2) and doxorubicin at different concentrations (0, 2, 4 and 8 µg/ml). The effects of oncolytic HSV1-hGM-CSF and doxorubicin on the tumor growth, survival time and their side effects on the mouse breast cancer model were observed.

Results:

Both oncolytic HSV1-hGM-CSF and doxorubicin significantly inhibited the proliferation of 4T1 cells in vitro. Doxorubicin induced the G(2)/M phase arrest of 4T1 cells, while the cytotoxicity of oncolytic HSV1-hGM-CSF was no cell cycle-dependent.At day 16 after treatment with doxorubicin and HSV1-hGM-CSF, the tumor volume of 4T1 tumor bearing mice were (144.40±27.68)mm(3,) (216.80±57.18)mm(3,) (246.10±21.90)mm(3,) (327.50±44.24)mm(3,) (213.30±32.31)mm(3) and (495.80±75.87)mm(3) in the groups of doxorubicin combined with high dose HSV1-hGM-CSF, doxorubicin combined with low dose HSV1-hGM-CSF, doxorubicin alone, high dose HSV1-hGM-CSF alone, low dose HSV1-hGM-CSF alone and control, respectively.Compared with the control group, both doxorubicin and HSV1-hGM-CSF treatment exhibited significant reduction of primary tumor volume in vivo (P<0.001). The median survival times were 48, 50, 40, 42, 43 and 37 days in the six groups mentioned above, respectively. The median survival period of doxorubicin alone, high dose HSV1-hGM-CSF alone and low dose HSV1-hGM-CSF alone were significantly longer than that of control (P<0.05).

Conclusion:

Synergistic effect of sequential treatment with doxorubicin and oncolytic HSV1-hGM-CSF is observed in 4T1 mouse breast cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Doxorrubicina / Factor Estimulante de Colonias de Granulocitos y Macrófagos / Herpesvirus Humano 1 / Neoplasias Mamarias Experimentales / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: Zh Revista: Zhonghua Zhong Liu Za Zhi Año: 2018 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Doxorrubicina / Factor Estimulante de Colonias de Granulocitos y Macrófagos / Herpesvirus Humano 1 / Neoplasias Mamarias Experimentales / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: Zh Revista: Zhonghua Zhong Liu Za Zhi Año: 2018 Tipo del documento: Article País de afiliación: China