Control of DNA replication and its potential clinical exploitation
- 20 January 2005
- journal article
- innovation
- Published by Springer Nature in Nature Reviews Cancer
- Vol. 5 (2) , 135-141
- https://doi.org/10.1038/nrc1548
Abstract
Multiple conserved mechanisms limit DNA replication to once per cell cycle. One vital level of control focuses on the loading of the heterohexameric ring of minichromosome maintenance proteins (MCMs) onto chromatin in the hierarchical assembly of the pre-replication complex at origins of replication. An essential role in proliferation for MCMs and their regulators makes them potentially important biomarkers for routine clinical use in cancer detection and prognosis.Keywords
This publication has 57 references indexed in Scilit:
- A novel immunohistochemical method for estimating cell cycle phase distribution in ovarian serous neoplasms: implications for the histopathological assessment of paraffin-embedded specimensBritish Journal of Cancer, 2004
- A novel immunohistochemical method to estimate cell‐cycle phase distribution in archival tissue: implications for the prediction of outcome in colorectal cancerThe Journal of Pathology, 2003
- Breast cancer classification and prognosis based on gene expression profiles from a population-based studyProceedings of the National Academy of Sciences, 2003
- Analysis of minichromosome maintenance proteins as a novel method for detection of colorectal cancer in stoolThe Lancet, 2002
- Gene expression profiling predicts clinical outcome of breast cancerNature, 2002
- Mammalian Orc1 Protein Is Selectively Released from Chromatin and Ubiquitinated during the S-to-M Transition in the Cell Division CycleMolecular and Cellular Biology, 2002
- The Roles of the MCM, ORC, and Cdc6 Proteins in Determining the Replication Competence of Chromatin in Quiescent CellsJournal of Structural Biology, 2000
- The Ki-67 protein: From the known and the unknownJournal of Cellular Physiology, 2000
- Cancer Cell CyclesScience, 1996
- Changes in cyclin/proliferating cell nuclear antigen distribution during DNA repair synthesis.The Journal of cell biology, 1988