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Cell kinetics of hypoxic cells in a murine tumour in vivo : flow cytometric determination of the radiation‐induced blockage of cell cycle progression
Author(s) -
Rutgers Derk H.,
Niessen Dorien P. P.,
Linden Pieter M.
Publication year - 1987
Publication title -
cell proliferation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.647
H-Index - 74
eISSN - 1365-2184
pISSN - 0960-7722
DOI - 10.1111/j.1365-2184.1987.tb01080.x
Subject(s) - cell cycle , flow cytometry , cell , biology , population , microbiology and biotechnology , immunology , biochemistry , medicine , environmental health
. Cells from the small cell population of viable cells in the large necrotic centre of murine M8013 tumours were investigated with respect to their cell kinetics. Flow cytometry (FCM) of this part of subcutaneously transplanted tumours revealed the presence of tumour cells with G1, S and G2 + M phase DNA‐contents. These severely hypoxic cells could have stopped cell cycle progression due to the nutritional deprivation, irrespective of their position within the cell cycle. Labelling methods, used to disclose the cell kinetics of this cell population, are hampered by the absence of a transport system in these large necrotic areas. Therefore, FCM was used to monitor radiation‐induced changes in the cell cycle distribution. From this investigation it was concluded that hypoxic cells in the necrotic centre of the M8013 tumour progress through the cell cycle. As well as a cell population with a cell cycle time (T c ) of approximately 84 hr, a subpopulation with a T c of approximately 21 hr occurred.

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