期刊
JOURNAL OF IMMUNOLOGY
卷 189, 期 3, 页码 1162-1172出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1102538
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资金
- Susan G. Komen for the Cure Investigator-Initiated Research Grant [KG090250]
- National Agency of Scientific Promotion of Argentina [IDB/PICT 2010-211]
- Argentina National Council of Scientific Research [PIP 737]
- Fundacion A. Roemmers
- Oncomed-Reno Consejo Nacional de Investigaciones Cientificas y Tecnicas de Argentina from Henry Moore Institute of Argentina [1819/03]
Aberrant Stat3 activation and signaling contribute to malignant transformation by promoting cell cycle progression, inhibiting apoptosis, and mediating tumor immune evasion. Stat3 inhibition in tumor cells induces the expression of chemokines and pro-inflammatory cytokines, so we proposed to apply Stat3-inhibited breast cancer cells as a source of immunogens to induce an antitumor immune response. Studies were performed in two murine breast cancer models in which Stat3 is activated: progestin-dependent C4HD cells and 4T1 cells. We immunized BALB/c mice with irradiated cancer cells previously transfected with a dominant-negative Stat3 vector (Stat3Y705F) in either a prophylactic or a therapeutic manner. Prophylactic administration of breast cancer cells transfected with Stat3Y705F (Stat3Y705F-breast cancer cells) inhibited primary tumor growth compared with administration of empty vector-transfected cells in both models. In the 4T1 model, 50% of the challenged mice were tumor free, and the incidence of metastasis decreased by 90%. In vivo assays of C4HD tumors showed that the antitumor immune response involves the participation of CD4(+) T cells and cytotoxic NK cells. Therapeutic immunization with Stat3Y705F-breast cancer cells inhibited tumor growth, promoted tumor cell differentiation, and decreased metastasis. Furthermore, inhibition of Stat3 activation in breast cancer cells induced cellular senescence, contributing to their immunogenic phenotype. In this work, we provide preclinical proof of concept that ablating Stat3 signaling in breast cancer cells results in an effective immunotherapy against breast cancer growth and metastasis. Moreover, our findings showing that Stat3 inactivation results in induction of a cellular senescence program disclose a potential mechanism for immunotherapy research. The Journal of Immunology, 2012, 189: 1162-1172.
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