13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Negative regulators of STAT3 signaling pathway in cancers

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          STAT3 is the most ubiquitous member of the STAT family and involved in many biological processes, such as cell proliferation, differentiation, and apoptosis. Mounting evidence has revealed that STAT3 is aberrantly activated in many malignant tumors and plays a critical role in cancer progression. STAT3 is usually regarded as an effective molecular target for cancer treatment, and abolishing the STAT3 activity may diminish tumor growth and metastasis. Recent studies have shown that negative regulators of STAT3 signaling such as PIAS, SOCS, and PTP, can effectively retard tumor progression. However, PIAS, SOCS, and PTP have also been reported to correlate with tumor malignancy, and their biological function in tumorigenesis and antitumor therapy are somewhat controversial. In this review, we summarize actual knowledge on the negative regulators of STAT3 in tumors, and focus on the potential role of PIAS, SOCS, and PTP in cancer treatment. Furthermore, we also outline the STAT3 inhibitors that have entered clinical trials. Targeting STAT3 seems to be a promising strategy in cancer therapy.

          Related collections

          Most cited references146

          • Record: found
          • Abstract: found
          • Article: not found

          Stattic: a small-molecule inhibitor of STAT3 activation and dimerization.

          Signal transducers and activators of transcription (STATs) are a family of latent cytoplasmic transcription factors that transmit signals from the cell membrane to the nucleus. One family member, STAT3, is constitutively activated by aberrant upstream tyrosine kinase activities in a broad spectrum of cancer cell lines and human tumors. Screening of chemical libraries led to the identification of Stattic, a nonpeptidic small molecule shown to selectively inhibit the function of the STAT3 SH2 domain regardless of the STAT3 activation state in vitro. Stattic selectively inhibits activation, dimerization, and nuclear translocation of STAT3 and increases the apoptotic rate of STAT3-dependent breast cancer cell lines. We propose Stattic as a tool for the inhibition of STAT3 in cell lines or animal tumor models displaying constitutive STAT3 activation.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Selective chemical probe inhibitor of Stat3, identified through structure-based virtual screening, induces antitumor activity.

            S3I-201 (NSC 74859) is a chemical probe inhibitor of Stat3 activity, which was identified from the National Cancer Institute chemical libraries by using structure-based virtual screening with a computer model of the Stat3 SH2 domain bound to its Stat3 phosphotyrosine peptide derived from the x-ray crystal structure of the Stat3beta homodimer. S3I-201 inhibits Stat3.Stat3 complex formation and Stat3 DNA-binding and transcriptional activities. Furthermore, S3I-201 inhibits growth and induces apoptosis preferentially in tumor cells that contain persistently activated Stat3. Constitutively dimerized and active Stat3C and Stat3 SH2 domain rescue tumor cells from S3I-201-induced apoptosis. Finally, S3I-201 inhibits the expression of the Stat3-regulated genes encoding cyclin D1, Bcl-xL, and survivin and inhibits the growth of human breast tumors in vivo. These findings strongly suggest that the antitumor activity of S3I-201 is mediated in part through inhibition of aberrant Stat3 activation and provide the proof-of-concept for the potential clinical use of Stat3 inhibitors such as S3I-201 in tumors harboring aberrant Stat3.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Protein-tyrosine phosphatases and cancer.

              Tyrosine phosphorylation is an important signalling mechanism in eukaryotic cells. In cancer, oncogenic activation of tyrosine kinases is a common feature, and novel anticancer drugs have been introduced that target these enzymes. Tyrosine phosphorylation is also controlled by protein-tyrosine phosphatases (PTPs). Recent evidence has shown that PTPs can function as tumour suppressors. In addition, some PTPs, including SHP2, positively regulate the signalling of growth-factor receptors, and can be oncogenic. An improved understanding of how these enzymes function and how they are regulated might aid the development of new anticancer agents.
                Bookmark

                Author and article information

                Journal
                Cancer Manag Res
                Cancer Manag Res
                CMAR
                cancmanres
                Cancer Management and Research
                Dove
                1179-1322
                29 May 2019
                2019
                : 11
                : 4957-4969
                Affiliations
                [1 ]College of Pharmacy, Dalian Medical University , Dalian 116044, People’s Republic of China
                [2 ]College of Basic Medical Sciences, Dalian Medical University , Dalian 116044, People’s Republic of China
                [3 ]Surgery Department of Dalian Municipal Central Hospital, Dalian Medical University , Dalian 116033, People’s Republic of China
                Author notes
                Correspondence: Xiaohong ShuCollege of Pharmacy, Dalian Medical University , 9 West Section, Lvshun South Road, Dalian116044, People’s Republic of ChinaTel +86-411-86110419Email xiaohong_shu@ 123456dmu.edu.cn
                Changle Ren Surgery Department of Dalian Municipal Central Hospital, Dalian Medical University , 826 Southwest Road, Dalian116033, People’s Republic of China Tel +86-411-84412001Email changlerenle@ 123456163.com
                [*]

                These authors contributed equally to this work

                Article
                206175
                10.2147/CMAR.S206175
                6549392
                4210e00c-dc50-409f-9bde-001cfa3852b5
                © 2019 Wu et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 21 February 2019
                : 17 April 2019
                Page count
                Figures: 2, Tables: 1, References: 173, Pages: 13
                Categories
                Review

                Oncology & Radiotherapy
                cancer,stat3 signaling,pias,socs,ptp,negative regulators
                Oncology & Radiotherapy
                cancer, stat3 signaling, pias, socs, ptp, negative regulators

                Comments

                Comment on this article