The Growth of Murine Lymphomatous Tumour-cells as Determined by Host Survival-time

Summary (1) A cell-dose-survival-time method of study has been developed for the LSA ascites lymphoma of C57Bl/Ka mice for the intraperitoneal and intravenous inoculation of tumour-cells. (2) A growth-model using survival-time as end-point has been experimentally studied. The generation time, as det...

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Veröffentlicht in:Intern. J. Radiation Biol 1964, Vol.8 (1), p.59-73
Hauptverfasser: Maruyama, Yosh, Brown, Jr, Byron Wm
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description Summary (1) A cell-dose-survival-time method of study has been developed for the LSA ascites lymphoma of C57Bl/Ka mice for the intraperitoneal and intravenous inoculation of tumour-cells. (2) A growth-model using survival-time as end-point has been experimentally studied. The generation time, as determined indirectly by survival-time, conforms with estimates of this parameter by direct means and suggests that murine lymphomatous tumour-cells grow exponentially during much of their growth in vivo under a given set of conditions. The mean rate of tumour-cell growth may differ according to site of growth. Death apparently occurs at a critical tumour-cell number in the range of inocula studied. (3) Methods are described for the handling of the experimental data, for the estimation of the generation time, for the threshold number of tumour-cells which, when present in the host, may result in its death. (4) Whole-body x-irradiation given after the inoculation of the tumour-cells will prolong the survival-time by predictable periods of time.
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(2) A growth-model using survival-time as end-point has been experimentally studied. The generation time, as determined indirectly by survival-time, conforms with estimates of this parameter by direct means and suggests that murine lymphomatous tumour-cells grow exponentially during much of their growth in vivo under a given set of conditions. The mean rate of tumour-cell growth may differ according to site of growth. Death apparently occurs at a critical tumour-cell number in the range of inocula studied. (3) Methods are described for the handling of the experimental data, for the estimation of the generation time, for the threshold number of tumour-cells which, when present in the host, may result in its death. 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J. Radiation Biol</title><addtitle>Int J Radiat Biol Relat Stud Phys Chem Med</addtitle><description>Summary (1) A cell-dose-survival-time method of study has been developed for the LSA ascites lymphoma of C57Bl/Ka mice for the intraperitoneal and intravenous inoculation of tumour-cells. (2) A growth-model using survival-time as end-point has been experimentally studied. The generation time, as determined indirectly by survival-time, conforms with estimates of this parameter by direct means and suggests that murine lymphomatous tumour-cells grow exponentially during much of their growth in vivo under a given set of conditions. The mean rate of tumour-cell growth may differ according to site of growth. Death apparently occurs at a critical tumour-cell number in the range of inocula studied. (3) Methods are described for the handling of the experimental data, for the estimation of the generation time, for the threshold number of tumour-cells which, when present in the host, may result in its death. 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J. Radiation Biol</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maruyama, Yosh</au><au>Brown, Jr, Byron Wm</au><aucorp>Stanford Univ., Calif</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Growth of Murine Lymphomatous Tumour-cells as Determined by Host Survival-time</atitle><jtitle>Intern. J. Radiation Biol</jtitle><addtitle>Int J Radiat Biol Relat Stud Phys Chem Med</addtitle><date>1964</date><risdate>1964</risdate><volume>8</volume><issue>1</issue><spage>59</spage><epage>73</epage><pages>59-73</pages><issn>0955-3002</issn><issn>0020-7616</issn><eissn>1362-3095</eissn><abstract>Summary (1) A cell-dose-survival-time method of study has been developed for the LSA ascites lymphoma of C57Bl/Ka mice for the intraperitoneal and intravenous inoculation of tumour-cells. (2) A growth-model using survival-time as end-point has been experimentally studied. The generation time, as determined indirectly by survival-time, conforms with estimates of this parameter by direct means and suggests that murine lymphomatous tumour-cells grow exponentially during much of their growth in vivo under a given set of conditions. The mean rate of tumour-cell growth may differ according to site of growth. Death apparently occurs at a critical tumour-cell number in the range of inocula studied. (3) Methods are described for the handling of the experimental data, for the estimation of the generation time, for the threshold number of tumour-cells which, when present in the host, may result in its death. (4) Whole-body x-irradiation given after the inoculation of the tumour-cells will prolong the survival-time by predictable periods of time.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>14190708</pmid><doi>10.1080/09553006414550061</doi><tpages>15</tpages></addata></record>
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source MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete
subjects ANIMAL CELLS
Animals
BIOLOGY AND MEDICINE
BODY
CATTLE
Cell Division
DEATH
ENVIRONMENT
EXPANSION
GROWTH
IN VIVO
INJECTION
Injections
Injections, Intraperitoneal
Injections, Intravenous
IRRADIATION
LYMPH SYSTEM
Lymphoma
MICE
MOCKUP
Neoplasms - radiotherapy
Neoplasms, Experimental
PARASITES
QUANTITATIVE ANALYSIS
QUANTITY RATIO
Radiation Effects
REPRODUCTION
Statistics as Topic
SURVIVAL
SURVIVAL TIME
Transplantation
TUMORS
X RADIATION
title The Growth of Murine Lymphomatous Tumour-cells as Determined by Host Survival-time
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