The University of Southampton
University of Southampton Institutional Repository

Cell production rates in human tissues and tumours and their significance. Part II: clinical data

Cell production rates in human tissues and tumours and their significance. Part II: clinical data
Cell production rates in human tissues and tumours and their significance. Part II: clinical data
This paper reviews the available data for cell production rates of human tissues and tumours, measured in vivo using halogenated pyrimidine labelling and laser cytometry. The technique has now been widely evaluated, and we draw general inferences from the proliferative data over a broad range of tumour and tissue types. Estimates of the S-phase duration, the time taken for DNA synthesis in cycling cells, are consistent over a narrow range with a median value of around 10 hours, notwithstanding the constraints of the experimental and statistical technique, in normal tissues and tumours. This suggests that Ts values may be a species-specific constant. The more easily measured labelled S-phase fraction, or labelling index, shows much greater intra and intertumour variation within any one tumour class. It may thus be a surrogate for time dependent measurements to a first order approximation. The cell production rate, described by the potential doubling time (Tpot), is remarkably rapid in most tumours, a median value of the order of 5 days, and much faster than clinical volume doubling times for most lesions. The rapid cell production rates in normal tissues and tumours highlight the importance of cell loss in the growth and modelling of biological structures. Cell production rate measurements do not adequately describe the biological aggressiveness of tumours. They may be used to refine adjuvant strategies for radiotherapy and chemotherapy in experimental research. Dynamic halogenated pyrimidine labelling has provided unique and valuable insights into the living biology of human tissues and tumours.
Bromodeoxyuridine, Cancer, Cell proliferation, Clinical outcome, Flow cytometry, Iododeoxyuridine, Prognosis
0748-7983
405-417
Rew, D. A.
36dcc3ad-2379-4b61-a468-5c623d796887
George D Wilson
Rew, D. A.
36dcc3ad-2379-4b61-a468-5c623d796887

George D Wilson (2000) Cell production rates in human tissues and tumours and their significance. Part II: clinical data. European Journal of Surgical Oncology, 26 (4), 405-417. (doi:10.1053/ejso.1999.0907).

Record type: Review

Abstract

This paper reviews the available data for cell production rates of human tissues and tumours, measured in vivo using halogenated pyrimidine labelling and laser cytometry. The technique has now been widely evaluated, and we draw general inferences from the proliferative data over a broad range of tumour and tissue types. Estimates of the S-phase duration, the time taken for DNA synthesis in cycling cells, are consistent over a narrow range with a median value of around 10 hours, notwithstanding the constraints of the experimental and statistical technique, in normal tissues and tumours. This suggests that Ts values may be a species-specific constant. The more easily measured labelled S-phase fraction, or labelling index, shows much greater intra and intertumour variation within any one tumour class. It may thus be a surrogate for time dependent measurements to a first order approximation. The cell production rate, described by the potential doubling time (Tpot), is remarkably rapid in most tumours, a median value of the order of 5 days, and much faster than clinical volume doubling times for most lesions. The rapid cell production rates in normal tissues and tumours highlight the importance of cell loss in the growth and modelling of biological structures. Cell production rate measurements do not adequately describe the biological aggressiveness of tumours. They may be used to refine adjuvant strategies for radiotherapy and chemotherapy in experimental research. Dynamic halogenated pyrimidine labelling has provided unique and valuable insights into the living biology of human tissues and tumours.

This record has no associated files available for download.

More information

Published date: June 2000
Additional Information: Copyright: Copyright 2018 Elsevier B.V., All rights reserved.
Keywords: Bromodeoxyuridine, Cancer, Cell proliferation, Clinical outcome, Flow cytometry, Iododeoxyuridine, Prognosis

Identifiers

Local EPrints ID: 449509
URI: http://eprints.soton.ac.uk/id/eprint/449509
ISSN: 0748-7983
PURE UUID: 99bd6597-ce66-444a-8ba7-4a474d559737
ORCID for D. A. Rew: ORCID iD orcid.org/0000-0002-4518-2667

Catalogue record

Date deposited: 04 Jun 2021 16:31
Last modified: 17 Mar 2024 03:56

Export record

Altmetrics

Contributors

Author: D. A. Rew ORCID iD
Corporate Author: George D Wilson

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×