| Literature DB >> 21374075 |
Tomonori Yaguchi1, Hidetoshi Sumimoto2, Chie Kudo-Saito2, Nobuo Tsukamoto2, Ryo Ueda2, Tomoko Iwata-Kajihara2, Hiroshi Nishio2,3, Naoshi Kawamura2, Yutaka Kawakami2.
Abstract
Cancer-induced immunosuppression is a major problem as it reduces the anti-tumor effects of immunotherapies. In cancer tissues, cancer cells, immune cells, and other stromal cells interact and create an immunosuppressive microenvironment through a variety of immunosuppressive factors. Some cancer subpopulations such as cancer cells undergoing epithelial-mesenchymal transition and cancer stem-like cells have immunosuppressive and immunoresistant properties. The production of immunosuppressive factors by cancer cells is mechanistically attributed to oncogenic signals frequently activated in cancer cells, including the STAT3, MAPK, NF-κB, and Wnt/β-catenin signals, which are upstream events leading to immunosuppressive cascades. Moreover, some of these signals are also activated in immunosuppressive immune cells stimulated by cancer-derived factors and contribute to their immunosuppressive activities. Therefore, targeting these signals both in cancer cells and immunosuppressive immune cells may result in the restoration of immunocompetence in cancer patients and improve current immunotherapy.Entities:
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Year: 2011 PMID: 21374075 DOI: 10.1007/s12185-011-0799-6
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490