Literature DB >> 20517723

STAT3: a target to enhance antitumor immune response.

Heehyoung Lee1, Sumanta Kumar Pal, Karen Reckamp, Robert A Figlin, Hua Yu.   

Abstract

Signal transducer and activator of transcription 3 (Stat3) has emerged as a critical regulator for tumor-associated inflammation. Activation of Stat3 negatively regulates the Th1-type immune response and promotes expansion of myeloid-derived suppressor cells (MDSCs) and regulatory T-cell functions in the tumor microenvironment. Mounting evidence suggests that Stat3 and related pathways may serve as a target for changing the tumor immunologic microenvironment to benefit cancer immunotherapies. Many recent studies support the use of certain tyrosine kinase inhibitors, through inhibition of Stat3, in decreasing immunosuppression in the tumor microenvironment. Other potential therapeutic avenues include the use of targeted delivery of Stat3 siRNA into immune cells. Here, we describe the role of Stat3 in regulating the immunologic properties of tumors as a background for Stat3-based therapeutic interventions.

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Year:  2011        PMID: 20517723      PMCID: PMC3244828          DOI: 10.1007/82_2010_51

Source DB:  PubMed          Journal:  Curr Top Microbiol Immunol        ISSN: 0070-217X            Impact factor:   4.291


  105 in total

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Review 4.  Cancer immunoediting: from immunosurveillance to tumor escape.

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Authors:  Thomas Welte; Samuel S M Zhang; Tian Wang; Zhiyuan Zhang; David G T Hesslein; Zhinan Yin; Arihiro Kano; Yoshiki Iwamoto; En Li; Joseph E Craft; Alfred L M Bothwell; Erol Fikrig; Pandelakis A Koni; Richard A Flavell; Xin-Yuan Fu
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-05       Impact factor: 11.205

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Review 2.  Targeting the IL-6/JAK/STAT3 signalling axis in cancer.

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3.  STAT3 cyclic oligonucleotide decoy-a new therapeutic avenue for NSCLC?

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6.  Targeting STAT3 signaling reduces immunosuppressive myeloid cells in head and neck squamous cell carcinoma.

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Review 7.  Combining immunotherapy and targeted therapies in cancer treatment.

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9.  Deficiency of G-protein-coupled bile acid receptor Gpbar1 (TGR5) enhances chemically induced liver carcinogenesis.

Authors:  Wei-Dong Chen; Donna Yu; Barry M Forman; Wendong Huang; Yan-Dong Wang
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