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Role of STAT3 in Cancer Metastasis and Translational Advances

Signal transducer and activator of transcription 3 (STAT3) is a latent cytoplasmic transcription factor, originally discovered as a transducer of signal from cell surface receptors to the nucleus. It is activated by tyrosine phosphorylation at position 705 leading to its dimerization, nuclear transl...

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Detalles Bibliográficos
Autores principales: Kamran, Mohammad Zahid, Patil, Prachi, Gude, Rajiv P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807846/
https://www.ncbi.nlm.nih.gov/pubmed/24199193
http://dx.doi.org/10.1155/2013/421821
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author Kamran, Mohammad Zahid
Patil, Prachi
Gude, Rajiv P.
author_facet Kamran, Mohammad Zahid
Patil, Prachi
Gude, Rajiv P.
author_sort Kamran, Mohammad Zahid
collection PubMed
description Signal transducer and activator of transcription 3 (STAT3) is a latent cytoplasmic transcription factor, originally discovered as a transducer of signal from cell surface receptors to the nucleus. It is activated by tyrosine phosphorylation at position 705 leading to its dimerization, nuclear translocation, DNA binding, and activation of gene transcription. Under normal physiological conditions, STAT3 activation is tightly regulated. However, compelling evidence suggests that STAT3 is constitutively activated in many cancers and plays a pivotal role in tumor growth and metastasis. It regulates cellular proliferation, invasion, migration, and angiogenesis that are critical for cancer metastasis. In this paper, we first describe the mechanism of STAT3 regulation followed by how STAT3 is involved in cancer metastasis, then we summarize the various small molecule inhibitors that inhibit STAT3 signaling.
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spelling pubmed-38078462013-11-06 Role of STAT3 in Cancer Metastasis and Translational Advances Kamran, Mohammad Zahid Patil, Prachi Gude, Rajiv P. Biomed Res Int Review Article Signal transducer and activator of transcription 3 (STAT3) is a latent cytoplasmic transcription factor, originally discovered as a transducer of signal from cell surface receptors to the nucleus. It is activated by tyrosine phosphorylation at position 705 leading to its dimerization, nuclear translocation, DNA binding, and activation of gene transcription. Under normal physiological conditions, STAT3 activation is tightly regulated. However, compelling evidence suggests that STAT3 is constitutively activated in many cancers and plays a pivotal role in tumor growth and metastasis. It regulates cellular proliferation, invasion, migration, and angiogenesis that are critical for cancer metastasis. In this paper, we first describe the mechanism of STAT3 regulation followed by how STAT3 is involved in cancer metastasis, then we summarize the various small molecule inhibitors that inhibit STAT3 signaling. Hindawi Publishing Corporation 2013 2013-10-02 /pmc/articles/PMC3807846/ /pubmed/24199193 http://dx.doi.org/10.1155/2013/421821 Text en Copyright © 2013 Mohammad Zahid Kamran et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kamran, Mohammad Zahid
Patil, Prachi
Gude, Rajiv P.
Role of STAT3 in Cancer Metastasis and Translational Advances
title Role of STAT3 in Cancer Metastasis and Translational Advances
title_full Role of STAT3 in Cancer Metastasis and Translational Advances
title_fullStr Role of STAT3 in Cancer Metastasis and Translational Advances
title_full_unstemmed Role of STAT3 in Cancer Metastasis and Translational Advances
title_short Role of STAT3 in Cancer Metastasis and Translational Advances
title_sort role of stat3 in cancer metastasis and translational advances
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807846/
https://www.ncbi.nlm.nih.gov/pubmed/24199193
http://dx.doi.org/10.1155/2013/421821
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