Literature DB >> 19505186

Redox control of the cell cycle in health and disease.

Ehab H Sarsour1, Maneesh G Kumar, Leena Chaudhuri, Amanda L Kalen, Prabhat C Goswami.   

Abstract

The cellular oxidation and reduction (redox) environment is influenced by the production and removal of reactive oxygen species (ROS). In recent years, several reports support the hypothesis that cellular ROS levels could function as ''second messengers'' regulating numerous cellular processes, including proliferation. Periodic oscillations in the cellular redox environment, a redox cycle, regulate cell-cycle progression from quiescence (G(0)) to proliferation (G(1), S, G(2), and M) and back to quiescence. A loss in the redox control of the cell cycle could lead to aberrant proliferation, a hallmark of various human pathologies. This review discusses the literature that supports the concept of a redox cycle controlling the mammalian cell cycle, with an emphasis on how this control relates to proliferative disorders including cancer, wound healing, fibrosis, cardiovascular diseases, diabetes, and neurodegenerative diseases. We hypothesize that reestablishing the redox control of the cell cycle by manipulating the cellular redox environment could improve many aspects of the proliferative disorders.

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Year:  2009        PMID: 19505186      PMCID: PMC2783918          DOI: 10.1089/ars.2009.2513

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  361 in total

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Authors:  R H Burdon; V Gill
Journal:  Free Radic Res Commun       Date:  1993

3.  Antioxidant status in delayed healing type of wounds.

Authors:  A M Rasik; A Shukla
Journal:  Int J Exp Pathol       Date:  2000-08       Impact factor: 1.925

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5.  Effect of stromal and epithelial cells derived from normal and tumorous breast tissue on the proliferation of human breast cancer cell lines in co-culture.

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6.  A protective effect of pyrrolidine dithiocarbamate in a rat model of liver cirrhosis.

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7.  Different distributions of selenoprotein W and thioredoxin during postnatal brain development and embryogenesis.

Authors:  Dae-won Jeong; Eun Hae Kim; Tae Soo Kim; Youn Wook Chung; Hyun Kim; Ick Young Kim
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8.  Evidence that high telomerase activity may induce a senescent-like growth arrest in human fibroblasts.

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Review 9.  Development and consequences of insulin resistance: lessons from animals with hyperinsulinaemia.

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Journal:  Diabetes Metab       Date:  1996-04       Impact factor: 6.041

Review 10.  Are oxidative stress-activated signaling pathways mediators of insulin resistance and beta-cell dysfunction?

Authors:  Joseph L Evans; Ira D Goldfine; Betty A Maddux; Gerold M Grodsky
Journal:  Diabetes       Date:  2003-01       Impact factor: 9.461

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  126 in total

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Review 2.  Modifying radiation damage.

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Review 5.  Utilizing Superoxide Dismutase Mimetics to Enhance Radiation Therapy Response While Protecting Normal Tissues.

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7.  Ras-induced ROS upregulation affecting cell proliferation is connected with cell type-specific alterations of HSF1/SESN3/p21Cip1/WAF1 pathways.

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8.  Hypoxia-induced glucose-6-phosphate dehydrogenase overexpression and -activation in pulmonary artery smooth muscle cells: implication in pulmonary hypertension.

Authors:  Sukrutha Chettimada; Rakhee Gupte; Dhwajbahadur Rawat; Sarah A Gebb; Ivan F McMurtry; Sachin A Gupte
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Review 9.  ROS homeostasis during development: an evolutionary conserved strategy.

Authors:  Jos H M Schippers; Hung M Nguyen; Dandan Lu; Romy Schmidt; Bernd Mueller-Roeber
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10.  KRIT1 regulates the homeostasis of intracellular reactive oxygen species.

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