Mechanisms of disease: Insights into the emerging role of signal transducers and activators of transcription in cancer - PubMed (original) (raw)
Review
Mechanisms of disease: Insights into the emerging role of signal transducers and activators of transcription in cancer
Eric B Haura et al. Nat Clin Pract Oncol. 2005 Jun.
Abstract
Members of the signal transducers and activators of transcription (STAT) pathway, which were originally identified as key components linking cytokine signals to transcriptional events in cells, have recently been demonstrated to have a major role in cancer. They are cytoplasmic proteins that form functional dimers with each other when activated by tyrosine phosphorylation. Activated STAT proteins translocate to the nucleus to regulate expression of genes by binding to specific elements within gene promoters. Constitutive activation of the STAT family members Stat3 and Stat5, and/or loss of Stat1 signaling, is found in a large group of diverse tumors. Increasing evidence demonstrates that STAT proteins can regulate many pathways important in oncogenesis including cell-cycle progression, apoptosis, tumor angiogenesis, tumor-cell invasion and metastasis, and tumor-cell evasion of the immune system. Based on these findings, a growing effort is underway to target STAT proteins directly and indirectly for cancer therapy. This review will highlight STAT signaling pathways, STAT target genes involved in cancer, evidence for STAT activation in human cancers, and therapeutic strategies to target STAT molecules for anticancer therapy.
Similar articles
- Activated STAT signaling in human tumors provides novel molecular targets for therapeutic intervention.
Buettner R, Mora LB, Jove R. Buettner R, et al. Clin Cancer Res. 2002 Apr;8(4):945-54. Clin Cancer Res. 2002. PMID: 11948098 Review. - The role of STATs in transcriptional control and their impact on cellular function.
Bromberg J, Darnell JE Jr. Bromberg J, et al. Oncogene. 2000 May 15;19(21):2468-73. doi: 10.1038/sj.onc.1203476. Oncogene. 2000. PMID: 10851045 Review. - STAT proteins: from normal control of cellular events to tumorigenesis.
Calò V, Migliavacca M, Bazan V, Macaluso M, Buscemi M, Gebbia N, Russo A. Calò V, et al. J Cell Physiol. 2003 Nov;197(2):157-68. doi: 10.1002/jcp.10364. J Cell Physiol. 2003. PMID: 14502555 Review. - STAT proteins: novel molecular targets for cancer drug discovery.
Turkson J, Jove R. Turkson J, et al. Oncogene. 2000 Dec 27;19(56):6613-26. doi: 10.1038/sj.onc.1204086. Oncogene. 2000. PMID: 11426647 Review. - STATs in oncogenesis.
Bowman T, Garcia R, Turkson J, Jove R. Bowman T, et al. Oncogene. 2000 May 15;19(21):2474-88. doi: 10.1038/sj.onc.1203527. Oncogene. 2000. PMID: 10851046 Review.
Cited by
- Selective inhibition of STAT3 signaling using monobodies targeting the coiled-coil and N-terminal domains.
La Sala G, Michiels C, Kükenshöner T, Brandstoetter T, Maurer B, Koide A, Lau K, Pojer F, Koide S, Sexl V, Dumoutier L, Hantschel O. La Sala G, et al. Nat Commun. 2020 Aug 17;11(1):4115. doi: 10.1038/s41467-020-17920-z. Nat Commun. 2020. PMID: 32807795 Free PMC article. - Inflammation and oncogenesis: a vicious connection.
Grivennikov SI, Karin M. Grivennikov SI, et al. Curr Opin Genet Dev. 2010 Feb;20(1):65-71. doi: 10.1016/j.gde.2009.11.004. Epub 2009 Dec 25. Curr Opin Genet Dev. 2010. PMID: 20036794 Free PMC article. Review. - Significance and relationship between Cripto-1 and p-STAT3 expression in gastric cancer and precancerous lesions.
Zhang JG, Zhao J, Xin Y. Zhang JG, et al. World J Gastroenterol. 2010 Feb 7;16(5):571-7. doi: 10.3748/wjg.v16.i5.571. World J Gastroenterol. 2010. PMID: 20128024 Free PMC article. - Signal transducer and activator of transcription (STAT)-5: an opportunity for drug development in oncohematology.
Recio C, Guerra B, Guerra-Rodríguez M, Aranda-Tavío H, Martín-Rodríguez P, de Mirecki-Garrido M, Brito-Casillas Y, García-Castellano JM, Estévez-Braun A, Fernández-Pérez L. Recio C, et al. Oncogene. 2019 Jun;38(24):4657-4668. doi: 10.1038/s41388-019-0752-3. Epub 2019 Feb 19. Oncogene. 2019. PMID: 30783189 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous