Transcription and cancer
- PMID: 1645561
- PMCID: PMC1972398
- DOI: 10.1038/bjc.1991.151
Transcription and cancer
Abstract
The normal growth, development and function of an organism requires precise and co-ordinated control of gene expression. A major part of this control is exerted by regulating messenger RNA (mRNA) production and involves complex interactions between an array of transcriptionally active proteins and specific regulatory DNA sequences. The combination of such proteins and DNA sequences is specific for given gene or group of genes in a particular cell type and the proteins regulating the same gene may vary between cell types. In addition the expression or activity of these regulatory proteins may be modified depending on the state of differentiation of a cell or in response to an external stimulus. Thus, the differentiation of embryonic cells into diverse tissues is achieved and the mature structure and function of the organism is maintained. This review focusses on the role of perturbations of these transcriptional controls in neoplasia. Deregulation of transcription may result in the failure to express genes responsible for cellular differentiation, or alternatively, in the transcription of genes involved in cell division, through the inappropriate expression or activation of positively acting transcription factors and nuclear oncogenes. Whether the biochemical abnormalities that lead to the disordered growth and differentiation of a malignant tumour affect cell surface receptors, membrane or cytoplasmic signalling proteins or nuclear transcription factors, the end result is the inappropriate expression of some genes and failure to express others. Current research is starting to elucidate which of the elements of this complicated system are important in neoplasia.
Similar articles
-
Characterization of an early growth response gene, which encodes a zinc finger transcription factor, potentially involved in cell cycle regulation.Mol Endocrinol. 1995 Nov;9(11):1610-20. doi: 10.1210/mend.9.11.8584037. Mol Endocrinol. 1995. PMID: 8584037
-
The organization of the BCL6 gene.Leukemia. 1994 Aug;8(8):1327-30. Leukemia. 1994. PMID: 8057668
-
Differentiation primary response genes and proto-oncogenes as positive and negative regulators of terminal hematopoietic cell differentiation.Stem Cells. 1994 Jul;12(4):352-69. doi: 10.1002/stem.5530120402. Stem Cells. 1994. PMID: 7951003 Review.
-
Clone pAT 133 identifies a gene that encodes another human member of a class of growth factor-induced genes with almost identical zinc-finger domains.Proc Natl Acad Sci U S A. 1991 Nov 15;88(22):10079-83. doi: 10.1073/pnas.88.22.10079. Proc Natl Acad Sci U S A. 1991. PMID: 1658795 Free PMC article.
-
Steroid hormone regulation of nuclear proto-oncogenes.Endocr Rev. 1993 Dec;14(6):659-69. doi: 10.1210/edrv-14-6-659. Endocr Rev. 1993. PMID: 8119231 Review.
Cited by
-
A Novel NFIX-STAT6 Gene Fusion in Solitary Fibrous Tumor: A Case Report.Int J Mol Sci. 2021 Jul 13;22(14):7514. doi: 10.3390/ijms22147514. Int J Mol Sci. 2021. PMID: 34299133 Free PMC article.
-
Architecture in 3D cell culture: An essential feature for in vitro toxicology.Toxicol In Vitro. 2017 Dec;45(Pt 3):287-295. doi: 10.1016/j.tiv.2017.03.012. Epub 2017 Mar 30. Toxicol In Vitro. 2017. PMID: 28366709 Free PMC article. Review.
-
Gene networks and chromatin and transcriptional regulation of the phaseolin promoter in Arabidopsis.Plant Cell. 2013 Jul;25(7):2601-17. doi: 10.1105/tpc.113.112714. Epub 2013 Jul 19. Plant Cell. 2013. PMID: 23872538 Free PMC article.
-
Epigenetic diet: impact on the epigenome and cancer.Epigenomics. 2011 Aug;3(4):503-18. doi: 10.2217/epi.11.71. Epigenomics. 2011. PMID: 22022340 Free PMC article. Review.
-
Hepatic neoplasia: reflections and ruminations.Virchows Arch. 1995;427(1):1-18. doi: 10.1007/BF00203732. Virchows Arch. 1995. PMID: 7551337 Review. No abstract available.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources