Redox-mediated bypass of restriction point via skipping of G1pm
<p>Abstract</p> <p>Background</p> <p>It is well known that cancer cells bypass the restriction point, R, and undergo uncontrolled cell proliferation.</p> <p>Hypothesis and evidence</p> <p>We suggest here that fibrosarcoma cells enter G<sub>...
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doaj-160975927d59423d84dd0f3380120a502020-11-25T00:18:44ZengBMCTheoretical Biology and Medical Modelling1742-46822006-07-01312610.1186/1742-4682-3-26Redox-mediated bypass of restriction point via skipping of G1pmGreene James JHoffman ArnoldSpetner Lee MBurke Michael<p>Abstract</p> <p>Background</p> <p>It is well known that cancer cells bypass the restriction point, R, and undergo uncontrolled cell proliferation.</p> <p>Hypothesis and evidence</p> <p>We suggest here that fibrosarcoma cells enter G<sub>1ps </sub>directly from M, skipping G<sub>1pm</sub>, <it/>hence <it/>bypassing R, in response to redox modulation. Evidence is presented from the published literature that demonstrate a shortening of the cycle period of transformed fibroblasts (SV-3T3) compared to the nontransformed 3T3 fibroblasts, corresponding to the duration of G<sub>1pm </sub>in the 3T3 fibroblasts. Evidence is also presented that demonstrate that redox modulation can induce the CUA-4 fibroblasts to bypass R, resulting in a cycle period closely corresponding to the cycle period of fibrosarcoma cells (HT1080).</p> <p>Conclusion</p> <p>The evidence supports our hypothesis that a low internal redox potential can cause fibrosarcoma cells to skip the G<sub>1pm </sub>phase of the cell cycle.</p> http://www.tbiomed.com/content/3/1/26 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Greene James J Hoffman Arnold Spetner Lee M Burke Michael |
spellingShingle |
Greene James J Hoffman Arnold Spetner Lee M Burke Michael Redox-mediated bypass of restriction point via skipping of G1pm Theoretical Biology and Medical Modelling |
author_facet |
Greene James J Hoffman Arnold Spetner Lee M Burke Michael |
author_sort |
Greene James J |
title |
Redox-mediated bypass of restriction point via skipping of G1pm |
title_short |
Redox-mediated bypass of restriction point via skipping of G1pm |
title_full |
Redox-mediated bypass of restriction point via skipping of G1pm |
title_fullStr |
Redox-mediated bypass of restriction point via skipping of G1pm |
title_full_unstemmed |
Redox-mediated bypass of restriction point via skipping of G1pm |
title_sort |
redox-mediated bypass of restriction point via skipping of g1pm |
publisher |
BMC |
series |
Theoretical Biology and Medical Modelling |
issn |
1742-4682 |
publishDate |
2006-07-01 |
description |
<p>Abstract</p> <p>Background</p> <p>It is well known that cancer cells bypass the restriction point, R, and undergo uncontrolled cell proliferation.</p> <p>Hypothesis and evidence</p> <p>We suggest here that fibrosarcoma cells enter G<sub>1ps </sub>directly from M, skipping G<sub>1pm</sub>, <it/>hence <it/>bypassing R, in response to redox modulation. Evidence is presented from the published literature that demonstrate a shortening of the cycle period of transformed fibroblasts (SV-3T3) compared to the nontransformed 3T3 fibroblasts, corresponding to the duration of G<sub>1pm </sub>in the 3T3 fibroblasts. Evidence is also presented that demonstrate that redox modulation can induce the CUA-4 fibroblasts to bypass R, resulting in a cycle period closely corresponding to the cycle period of fibrosarcoma cells (HT1080).</p> <p>Conclusion</p> <p>The evidence supports our hypothesis that a low internal redox potential can cause fibrosarcoma cells to skip the G<sub>1pm </sub>phase of the cell cycle.</p> |
url |
http://www.tbiomed.com/content/3/1/26 |
work_keys_str_mv |
AT greenejamesj redoxmediatedbypassofrestrictionpointviaskippingofg1pm AT hoffmanarnold redoxmediatedbypassofrestrictionpointviaskippingofg1pm AT spetnerleem redoxmediatedbypassofrestrictionpointviaskippingofg1pm AT burkemichael redoxmediatedbypassofrestrictionpointviaskippingofg1pm |
_version_ |
1725374789616402432 |