Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.

Cancer is a complex, multi-step process characterized by misregulated signal transduction and altered metabolism. Cancer cells divide faster than normal cells and their growth rates have been reported to correlate with increased metabolic flux during cell transformation. Here we report on progressiv...

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Main Authors: Sarit Mizrachy-Schwartz, Nataly Kravchenko-Balasha, Hannah Ben-Bassat, Shoshana Klein, Alexander Levitzki
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC1913554?pdf=render
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spelling doaj-1e25c1b5a7f6413682c6aeddb9aa6a482020-11-25T01:06:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032007-01-0127e62810.1371/journal.pone.0000628Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.Sarit Mizrachy-SchwartzNataly Kravchenko-BalashaHannah Ben-BassatShoshana KleinAlexander LevitzkiCancer is a complex, multi-step process characterized by misregulated signal transduction and altered metabolism. Cancer cells divide faster than normal cells and their growth rates have been reported to correlate with increased metabolic flux during cell transformation. Here we report on progressive changes in essential elements of the biochemical network, in an in vitro model of transformation, consisting of primary human keratinocytes, human keratinocytes immortalized by human papillomavirus 16 (HPV16) and passaged repeatedly in vitro, and the extensively-passaged cells subsequently treated with the carcinogen benzo[a]pyrene. We monitored changes in cell growth, cell size and energy metabolism. The more transformed cells were smaller and divided faster, but the cellular energy flux was unchanged. During cell transformation the protein synthesis network contracted, as shown by the reduction in key cap-dependent translation factors. Moreover, there was a progressive shift towards internal ribosome entry site (IRES)-dependent translation. The switch from cap to IRES-dependent translation correlated with progressive activation of c-Src, an activator of AMP-activated protein kinase (AMPK), which controls energy-consuming processes, including protein translation. As cellular protein synthesis is a major energy-consuming process, we propose that the reduction in cell size and protein amount provide energy required for cell survival and proliferation. The cap to IRES-dependent switch seems to be part of a gradual optimization of energy-consuming mechanisms that redirects cellular processes to enhance cell growth, in the course of transformation.http://europepmc.org/articles/PMC1913554?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sarit Mizrachy-Schwartz
Nataly Kravchenko-Balasha
Hannah Ben-Bassat
Shoshana Klein
Alexander Levitzki
spellingShingle Sarit Mizrachy-Schwartz
Nataly Kravchenko-Balasha
Hannah Ben-Bassat
Shoshana Klein
Alexander Levitzki
Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.
PLoS ONE
author_facet Sarit Mizrachy-Schwartz
Nataly Kravchenko-Balasha
Hannah Ben-Bassat
Shoshana Klein
Alexander Levitzki
author_sort Sarit Mizrachy-Schwartz
title Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.
title_short Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.
title_full Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.
title_fullStr Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.
title_full_unstemmed Optimization of energy-consuming pathways towards rapid growth in HPV-transformed cells.
title_sort optimization of energy-consuming pathways towards rapid growth in hpv-transformed cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2007-01-01
description Cancer is a complex, multi-step process characterized by misregulated signal transduction and altered metabolism. Cancer cells divide faster than normal cells and their growth rates have been reported to correlate with increased metabolic flux during cell transformation. Here we report on progressive changes in essential elements of the biochemical network, in an in vitro model of transformation, consisting of primary human keratinocytes, human keratinocytes immortalized by human papillomavirus 16 (HPV16) and passaged repeatedly in vitro, and the extensively-passaged cells subsequently treated with the carcinogen benzo[a]pyrene. We monitored changes in cell growth, cell size and energy metabolism. The more transformed cells were smaller and divided faster, but the cellular energy flux was unchanged. During cell transformation the protein synthesis network contracted, as shown by the reduction in key cap-dependent translation factors. Moreover, there was a progressive shift towards internal ribosome entry site (IRES)-dependent translation. The switch from cap to IRES-dependent translation correlated with progressive activation of c-Src, an activator of AMP-activated protein kinase (AMPK), which controls energy-consuming processes, including protein translation. As cellular protein synthesis is a major energy-consuming process, we propose that the reduction in cell size and protein amount provide energy required for cell survival and proliferation. The cap to IRES-dependent switch seems to be part of a gradual optimization of energy-consuming mechanisms that redirects cellular processes to enhance cell growth, in the course of transformation.
url http://europepmc.org/articles/PMC1913554?pdf=render
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