Literature DB >> 9416785

Three A's of repopulation during fractionated irradiation of squamous epithelia: Asymmetry loss, Acceleration of stem-cell divisions and Abortive divisions.

W Dörr.   

Abstract

PURPOSE: To analyse the time-course and efficacy of repopulation in squamous epithelia, and to describe possible mechanisms of this regeneration response.
MATERIAL AND METHODS: Experimental and clinical studies of repopulation in squamous epithelia have been reviewed to outline general features of repopulation during fractionated radiotherapy.
RESULTS: Repopulation processes result in a relative increase in re-irradiation tolerance, which can be quantified as the dose equivalent compensated.
CONCLUSIONS: If the stem-cell concept is accepted, changes in residual tissue tolerance must be based on net production of stem cells. For this, normal asymmetrical stem-cell divisions that render equal numbers of stem cells and differentiating daughters, must turn into symmetrical divisions with the production of two stem cells. Furthermore, the rate of change in residual tolerance indicates that the stem-cell proliferation rate is increased. In addition to these changes in the stem-cell proliferation pattern, a limited number of divisions by sterilized cells contributes to overall cell production and maintenance of tissue function. A valid model of repopulation in squamous epithelia hence must be based on three distinct mechanisms summarized as the three A's: Asymmetry loss, Acceleration of stem-cell divisions, and Abortive divisions.

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Mesh:

Year:  1997        PMID: 9416785     DOI: 10.1080/095530097142780

Source DB:  PubMed          Journal:  Int J Radiat Biol        ISSN: 0955-3002            Impact factor:   2.694


  24 in total

1.  Monte Carlo radiotherapy simulations of accelerated repopulation and reoxygenation for hypoxic head and neck cancer.

Authors:  W M Harriss-Phillips; E Bezak; E K Yeoh
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2.  Influence of stem-cell cycle time on accelerated re-population during radiotherapy in head and neck cancer.

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Journal:  Cell Prolif       Date:  2012-07-07       Impact factor: 6.831

Review 3.  [Radiation biology of normal tissues. Scientific progress and perspectives].

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Review 4.  Radiation oncology in the era of precision medicine.

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Journal:  Nat Rev Cancer       Date:  2016-03-18       Impact factor: 60.716

5.  Modification of radiation-induced oral mucositis (mouse) by adult stem cell therapy: single-dose irradiation.

Authors:  Margret Schmidt; Aline Piro-Hussong; Annett Siegemund; Peggy Gabriel; Wolfgang Dörr
Journal:  Radiat Environ Biophys       Date:  2014-06-15       Impact factor: 1.925

6.  Radiation-induced oral mucositis in mice: strain differences.

Authors:  W Dörr; K Spekl; M Martin
Journal:  Cell Prolif       Date:  2002-08       Impact factor: 6.831

Review 7.  Radiogenomics: A systems biology approach to understanding genetic risk factors for radiotherapy toxicity?

Authors:  Carsten Herskind; Christopher J Talbot; Sarah L Kerns; Marlon R Veldwijk; Barry S Rosenstein; Catharine M L West
Journal:  Cancer Lett       Date:  2016-03-02       Impact factor: 8.679

8.  The diverse and complex roles of radiation on cancer treatment: therapeutic target and genome maintenance.

Authors:  Rajamanickam Baskar; Swee Peng Yap; Kevin Lee Min Chua; Koji Itahana
Journal:  Am J Cancer Res       Date:  2012-06-28       Impact factor: 6.166

9.  Dose-dependent uptake of 3'-deoxy-3'-[(18) F]fluorothymidine by the bowel after total-body irradiation.

Authors:  Markus Hartenbach; Andreas Delker; Sabrina Hartenbach; Juli Schlichtiger; Sabrina Niedermoser; Carmen Wängler; Björn Wängler; Guido Böning; Franz Josef Gildehaus; Klement Neumaier; Kirsten Lauber; Klaus Kraft; Claus Belka; Marcus Hacker; Viktor Meineke; Peter Bartenstein
Journal:  Mol Imaging Biol       Date:  2014-12       Impact factor: 3.488

10.  Radiobiological modeling of interplay between accelerated repopulation and altered fractionation schedules in head and neck cancer.

Authors:  Loredana G Marcu; Eva Bezak
Journal:  J Med Phys       Date:  2009-10
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