| Literature DB >> 15122590 |
Xiaoyan Shi1, Jianguo Liu, Zhaoying Xiang, Maki Mitsuhashi, Rita S Wu, Xiaojing Ma.
Abstract
Interleukin-12 (IL-12) has potent antitumor activities via natural killer cells and cytotoxic T lymphocytes. However, the molecular mechanisms whereby IL-12 induces tumoricidal activities are poorly understood. Here, we report the genome-wide analysis of gene expression in a primary murine mammary carcinoma model that resembles human breast cancer, following the therapeutic application of recombinant IL-12, which restricted tumor growth and metastasis. IL-12 was able to curtail neovascularization in the tumor as well as enhance the number of tumor-infiltrating lymphocytes. Comprehensive examination of global gene expression revealed IL-12-induced molecular changes associated with tumor regression and reduced lung metastasis, thus providing a high-resolution snapshot of a host response against a developing malignancy and a rich source of potential targets for therapeutic intervention of breast cancer. Copyright 2004 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 15122590 PMCID: PMC2957898 DOI: 10.1002/ijc.20145
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396