Comparison of flow and laser scanning cytometry for the assay of cell proliferation in human solid tumors
Comparison of flow and laser scanning cytometry for the assay of cell proliferation in human solid tumors
The introduction of the laser scanning cytometer offers new capabilities in cell proliferation research, through its capacity for validation of each and every cell event through direct visualization on the microscope slide. In this study, we report a direct comparison of proliferation data derived from flow and laser scanning cytometry of human tumor nuclei labeled in vivo with bromodeoxyuridine (BrdUrd). Nuclear suspensions from 19 invasive ductal breast carcinomas and 12 gastric adenocarcinomas were prepared and analysed for BrdUrd uptake and DNA content. Specimens were analysed using a FACScan and then prepared on cytocentrifuge preparations for laser scanning cytometry. DNA index, labeling index (LI), duration of S-phase (Ts) and potential doubling time (Tpot) were calculated using standard procedures. There was an excellent correlation between the two techniques in the calculation of DNA index (R = 0.983, P > 0.0001) and LI (R = 0.924, P > 0.0001). The Ts proved more problematical (R = 0.448, P = 0.0115) but the Tpot showed closer agreement (R = 0.851, P > 0.0001) as the LI was the dominant determinant of Tpot. No single parameter could be identified as the major source of variation between the two techniques. We conclude that the laser scanning cytometer produces data equivalent to that obtained by flow cytometry.
Flow cytometry, Human tumors, Laser scanning cytometry, Proliferation
355-361
Rew, David A.
36dcc3ad-2379-4b61-a468-5c623d796887
Reeve, Louise J.
4cded55c-5628-4ec0-aad7-fc8b1bb0f1f4
Wilson, George D.
7dc2682a-71fa-428f-91a5-a5100d62db77
6 January 1999
Rew, David A.
36dcc3ad-2379-4b61-a468-5c623d796887
Reeve, Louise J.
4cded55c-5628-4ec0-aad7-fc8b1bb0f1f4
Wilson, George D.
7dc2682a-71fa-428f-91a5-a5100d62db77
Abstract
The introduction of the laser scanning cytometer offers new capabilities in cell proliferation research, through its capacity for validation of each and every cell event through direct visualization on the microscope slide. In this study, we report a direct comparison of proliferation data derived from flow and laser scanning cytometry of human tumor nuclei labeled in vivo with bromodeoxyuridine (BrdUrd). Nuclear suspensions from 19 invasive ductal breast carcinomas and 12 gastric adenocarcinomas were prepared and analysed for BrdUrd uptake and DNA content. Specimens were analysed using a FACScan and then prepared on cytocentrifuge preparations for laser scanning cytometry. DNA index, labeling index (LI), duration of S-phase (Ts) and potential doubling time (Tpot) were calculated using standard procedures. There was an excellent correlation between the two techniques in the calculation of DNA index (R = 0.983, P > 0.0001) and LI (R = 0.924, P > 0.0001). The Ts proved more problematical (R = 0.448, P = 0.0115) but the Tpot showed closer agreement (R = 0.851, P > 0.0001) as the LI was the dominant determinant of Tpot. No single parameter could be identified as the major source of variation between the two techniques. We conclude that the laser scanning cytometer produces data equivalent to that obtained by flow cytometry.
This record has no associated files available for download.
More information
e-pub ahead of print date: 1 November 1998
Published date: 6 January 1999
Additional Information:
Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
Keywords:
Flow cytometry, Human tumors, Laser scanning cytometry, Proliferation
Identifiers
Local EPrints ID: 449514
URI: http://eprints.soton.ac.uk/id/eprint/449514
ISSN: 0196-4763
PURE UUID: 5ace7bf7-b6c8-4697-8dad-43bbe56d2156
Catalogue record
Date deposited: 04 Jun 2021 16:31
Last modified: 17 Mar 2024 03:56
Export record
Altmetrics
Contributors
Author:
Louise J. Reeve
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