Abstract
The interrelationship among external O2 and glucose supply, oxygenation status, oxygen consumption rates and cellular viability in tumour microregions was studied using the multicellular spheroid model. For chronic exposure to various supply conditions multicellular EMT6/Ro spheroids were cultured in stirred media equilibrated either with 20% (v/v) or 5% (v/v) oxygen and containing four different glucose concentrations ranging from 0.8 mM to 16.5 mM. Spheroids were investigated using histology and O2-sensitive microelectrodes for measuring oxygen tension (PO2) values. A chronic decrease of the glucose concentration in the medium is associated with a substantial reduction in the thickness of the viable rim of cells and with a persistent increase in the cellular respiration rate. In general, both viable rim size and respiration are decreased through restriction of O2 supply during spheroid growth at a given external glucose concentration. The O2 consumption in spheroids appears to decrease with increasing spheroid size under most of the growth conditions investigated. These findings provide evidence for a large capacity of the spheroid cells to chronically adapt their metabolic rates to different supply situations. The experimental data and theoretical considerations indicate that necrosis may develop in the centre of these spheroids due to the lack of O2 and/or glucose under some of the growth conditions, but central necrosis can also occur despite sufficient O2 and glucose supply. Consequently, cellular metabolism and viability in tumour microregions may not be determined by the diffusion limitation of O2 or specific substrates alone, such as glucose, but may be influenced by a complex interaction of factors in the micromilieu the majority of which are still unknown.
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Selected References
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- Angello J. C., Hosick H. L. Glycosaminoglycan synthesis by mammary tumor spheroids. Biochem Biophys Res Commun. 1982 Aug;107(3):1130–1137. doi: 10.1016/0006-291x(82)90639-8. [DOI] [PubMed] [Google Scholar]
- Balin A. K., Goodman B. P., Rasmussen H., Cristofalo V. J. The effect of oxygen tension on the growth and metabolism of WI-38 cells. J Cell Physiol. 1976 Oct;89(2):235–249. doi: 10.1002/jcp.1040890207. [DOI] [PubMed] [Google Scholar]
- Carlsson J., Stålnacke C. G., Acker H., Haji-Karim M., Nilsson S., Larsson B. The influence of oxygen on viability and proliferation in cellular spheroids. Int J Radiat Oncol Biol Phys. 1979 Nov-Dec;5(11-12):2011–2020. doi: 10.1016/0360-3016(79)90953-2. [DOI] [PubMed] [Google Scholar]
- Ceccarini C., Eagle H. pH as a determinant of cellular growth and contact inhibition. Proc Natl Acad Sci U S A. 1971 Jan;68(1):229–233. doi: 10.1073/pnas.68.1.229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crabtree H. G. Observations on the carbohydrate metabolism of tumours. Biochem J. 1929;23(3):536–545. doi: 10.1042/bj0230536. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dertinger H., Hülser D. Increased radioresistance of cells in cultured multicell spheroids. I. Dependence on cellular interaction. Radiat Environ Biophys. 1981;19(2):101–107. doi: 10.1007/BF01324226. [DOI] [PubMed] [Google Scholar]
- Franko A. J., Sutherland R. M. Oxygen diffusion distance and development of necrosis in multicell spheroids. Radiat Res. 1979 Sep;79(3):439–453. [PubMed] [Google Scholar]
- Franko A. J., Sutherland R. M. Radiation survival of cells from spheroids grown in different oxygen concentrations. Radiat Res. 1979 Sep;79(3):454–467. [PubMed] [Google Scholar]
- Freyer J. P., Sutherland R. M. A reduction in the in situ rates of oxygen and glucose consumption of cells in EMT6/Ro spheroids during growth. J Cell Physiol. 1985 Sep;124(3):516–524. doi: 10.1002/jcp.1041240323. [DOI] [PubMed] [Google Scholar]
- Freyer J. P., Sutherland R. M. Selective dissociation and characterization of cells from different regions of multicell tumor spheroids. Cancer Res. 1980 Nov;40(11):3956–3965. [PubMed] [Google Scholar]
- Freyer J. P., Tustanoff E., Franko A. J., Sutherland R. M. In situ oxygen consumption rates of cells in V-79 multicellular spheroids during growth. J Cell Physiol. 1984 Jan;118(1):53–61. doi: 10.1002/jcp.1041180111. [DOI] [PubMed] [Google Scholar]
- Grossmann U., Winkler P., Carlsson J., Acker H. Local variations of oxygen consumption within multicellular spheroids calculated from measured PO2 profiles. Adv Exp Med Biol. 1984;169:719–728. doi: 10.1007/978-1-4684-1188-1_64. [DOI] [PubMed] [Google Scholar]
- Grote J., Süsskind R., Vaupel P. Oxygen diffusivity in tumor tissue (DS-carcinosarcoma) under temperature conditions within the range of 20--40 degrees C. Pflugers Arch. 1977 Nov 25;372(1):37–42. doi: 10.1007/BF00582204. [DOI] [PubMed] [Google Scholar]
- Gupta V., Eberle R. Modulation of tumour cell colony growth in soft agar by oxygen and its mechanism. Br J Cancer. 1984 May;49(5):587–593. doi: 10.1038/bjc.1984.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mueller-Klieser W. F., Sutherland R. M. Influence of convection in the growth medium on oxygen tensions in multicellular tumor spheroids. Cancer Res. 1982 Jan;42(1):237–242. [PubMed] [Google Scholar]
- Mueller-Klieser W. F., Sutherland R. M. Oxygen tensions in multicell spheroids of two cell lines. Br J Cancer. 1982 Feb;45(2):256–264. doi: 10.1038/bjc.1982.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mueller-Klieser W., Freyer J. P., Sutherland R. M. Evidence for a major role of glucose in controlling development of necrosis in EMT6/Ro multicell tumor spheroids. Adv Exp Med Biol. 1983;159:487–495. doi: 10.1007/978-1-4684-7790-0_42. [DOI] [PubMed] [Google Scholar]
- Mueller-Klieser W. Method for the determination of oxygen consumption rates and diffusion coefficients in multicellular spheroids. Biophys J. 1984 Sep;46(3):343–348. doi: 10.1016/S0006-3495(84)84030-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nederman T., Norling B., Glimelius B., Carlsson J., Brunk U. Demonstration of an extracellular matrix in multicellular tumor spheroids. Cancer Res. 1984 Jul;44(7):3090–3097. [PubMed] [Google Scholar]
- Poste G., Greig R. The experimental and clinical implications of cellular heterogeneity in malignant tumors. J Cancer Res Clin Oncol. 1983;106(3):159–170. doi: 10.1007/BF00402602. [DOI] [PubMed] [Google Scholar]
- Rockwell S. C., Kallman R. F., Fajardo L. F. Characteristics of a serially transplanted mouse mammary tumor and its tissue-culture-adapted derivative. J Natl Cancer Inst. 1972 Sep;49(3):735–749. [PubMed] [Google Scholar]
- Sutherland R. M., Durand R. E. Radiation response of multicell spheroids--an in vitro tumour model. Curr Top Radiat Res Q. 1976 Jan;11(1):87–139. [PubMed] [Google Scholar]
- THOMLINSON R. H., GRAY L. H. The histological structure of some human lung cancers and the possible implications for radiotherapy. Br J Cancer. 1955 Dec;9(4):539–549. doi: 10.1038/bjc.1955.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vaupel P. W., Frinak S., Bicher H. I. Heterogeneous oxygen partial pressure and pH distribution in C3H mouse mammary adenocarcinoma. Cancer Res. 1981 May;41(5):2008–2013. [PubMed] [Google Scholar]
- Wigle J. C., Freyer J. P., Sutherland R. M. Use of a sedimentation column to obtain uniformly sized populations of multicell spheroids. In Vitro. 1983 Apr;19(4):361–366. doi: 10.1007/BF02619514. [DOI] [PubMed] [Google Scholar]