Comparison of growth of human bladder cancer in tissue culture or as xenografts with clinical and pathological characteristics

Seventy-four biopsies of human bladder carcinoma were assessed by implantation as xenografts in immune-deprived mice and/or by culture of cell suspensions in agar or methylcellulose. The quality of the cell suspensions was assessed immediately after plating in vitro. The results were compared with t...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 1984-06, Vol.44 (6), p.2530-2533
Hauptverfasser: KOVNAT, A, BUICK, R. N, CONNOLLY, J. G, JEWETT, M. A, KERESTECI, A. G, TANNOCK, I. F
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container_end_page 2533
container_issue 6
container_start_page 2530
container_title Cancer research (Chicago, Ill.)
container_volume 44
creator KOVNAT, A
BUICK, R. N
CONNOLLY, J. G
JEWETT, M. A
KERESTECI, A. G
TANNOCK, I. F
description Seventy-four biopsies of human bladder carcinoma were assessed by implantation as xenografts in immune-deprived mice and/or by culture of cell suspensions in agar or methylcellulose. The quality of the cell suspensions was assessed immediately after plating in vitro. The results were compared with the pathological stage and grade of the biopsies and with the clinical course of the disease in patients from whom the biopsies were obtained. We found that (a) progressively growing xenografts were generated from 20 of 53 biopsies (38%). These xenografts grew with mean volume doubling times in the range of 1 to 3 weeks; all of them examined histologically were consistent with transitional cell carcinoma. (b) Colony formation occurred from 21 of 49 cell suspensions (43%), and plating efficiency was in the range of 0.0004 to 1.7%. The majority of cell suspensions were found to have residual small clusters of cells. Colony formation sometimes originated from these clusters, an effect that would be expected to introduce artifacts when the in vivo cloning assay is used for chemosensitivity testing. (c) There was no evident correlation between expression of clonal growth in vitro and success of xenografting, and no correlation between the results of either of these experimental procedures with stage, grade, or clinical course of the disease. Further improvements in tissue culture and xenograft technology will be required before these methods can be used as a guide to patient management.
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(b) Colony formation occurred from 21 of 49 cell suspensions (43%), and plating efficiency was in the range of 0.0004 to 1.7%. The majority of cell suspensions were found to have residual small clusters of cells. Colony formation sometimes originated from these clusters, an effect that would be expected to introduce artifacts when the in vivo cloning assay is used for chemosensitivity testing. (c) There was no evident correlation between expression of clonal growth in vitro and success of xenografting, and no correlation between the results of either of these experimental procedures with stage, grade, or clinical course of the disease. 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These xenografts grew with mean volume doubling times in the range of 1 to 3 weeks; all of them examined histologically were consistent with transitional cell carcinoma. (b) Colony formation occurred from 21 of 49 cell suspensions (43%), and plating efficiency was in the range of 0.0004 to 1.7%. The majority of cell suspensions were found to have residual small clusters of cells. Colony formation sometimes originated from these clusters, an effect that would be expected to introduce artifacts when the in vivo cloning assay is used for chemosensitivity testing. (c) There was no evident correlation between expression of clonal growth in vitro and success of xenografting, and no correlation between the results of either of these experimental procedures with stage, grade, or clinical course of the disease. Further improvements in tissue culture and xenograft technology will be required before these methods can be used as a guide to patient management.</description><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Transitional Cell - physiopathology</subject><subject>Cell Division</subject><subject>Cells, Cultured</subject><subject>Cytarabine - toxicity</subject><subject>Experimental renal and urinary tract tumors</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>Neoplasm Transplantation</subject><subject>Transplantation, Heterologous</subject><subject>Tumors</subject><subject>Urinary Bladder Neoplasms - physiopathology</subject><subject>Whole-Body Irradiation</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UEtLAzEQDqLUWv0JQg5eFza7SZM9SvFRKHjRc5m8upHdZEmyVC_-dqMWYeCbmW--eZ2hJWGtqDil7Bwt67oWFaO8uURXKb2XkJGaLdBi3fKm6-gSfW3COEF0KXgcLD7EcMz9j9fPI3gsB9DaRKzAqwLO4-xSmg1W85DnaHCIGBL-MD4cItic8NEVvRqcdwoGDF7jCXIfhnD4TageIqhsysTsVLpGFxaGZG5OuEJvjw-vm-dq9_K03dzvqr5Zi1xx1jZS1CA1ZULTVhNad8CBS0O4IIZ2VMvOaiLB1h2RxDJtGktNUTHBSLtCt399p1mORu-n6EaIn_vTHwp_d-IhlTVtLPe69F8mBC_G229eZGpH</recordid><startdate>19840601</startdate><enddate>19840601</enddate><creator>KOVNAT, A</creator><creator>BUICK, R. 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Experimental tumors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Transitional Cell - physiopathology</topic><topic>Cell Division</topic><topic>Cells, Cultured</topic><topic>Cytarabine - toxicity</topic><topic>Experimental renal and urinary tract tumors</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>Neoplasm Transplantation</topic><topic>Transplantation, Heterologous</topic><topic>Tumors</topic><topic>Urinary Bladder Neoplasms - physiopathology</topic><topic>Whole-Body Irradiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KOVNAT, A</creatorcontrib><creatorcontrib>BUICK, R. N</creatorcontrib><creatorcontrib>CONNOLLY, J. G</creatorcontrib><creatorcontrib>JEWETT, M. A</creatorcontrib><creatorcontrib>KERESTECI, A. G</creatorcontrib><creatorcontrib>TANNOCK, I. 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F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of growth of human bladder cancer in tissue culture or as xenografts with clinical and pathological characteristics</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1984-06-01</date><risdate>1984</risdate><volume>44</volume><issue>6</issue><spage>2530</spage><epage>2533</epage><pages>2530-2533</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Seventy-four biopsies of human bladder carcinoma were assessed by implantation as xenografts in immune-deprived mice and/or by culture of cell suspensions in agar or methylcellulose. The quality of the cell suspensions was assessed immediately after plating in vitro. The results were compared with the pathological stage and grade of the biopsies and with the clinical course of the disease in patients from whom the biopsies were obtained. We found that (a) progressively growing xenografts were generated from 20 of 53 biopsies (38%). These xenografts grew with mean volume doubling times in the range of 1 to 3 weeks; all of them examined histologically were consistent with transitional cell carcinoma. (b) Colony formation occurred from 21 of 49 cell suspensions (43%), and plating efficiency was in the range of 0.0004 to 1.7%. The majority of cell suspensions were found to have residual small clusters of cells. Colony formation sometimes originated from these clusters, an effect that would be expected to introduce artifacts when the in vivo cloning assay is used for chemosensitivity testing. (c) There was no evident correlation between expression of clonal growth in vitro and success of xenografting, and no correlation between the results of either of these experimental procedures with stage, grade, or clinical course of the disease. Further improvements in tissue culture and xenograft technology will be required before these methods can be used as a guide to patient management.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>6372994</pmid><tpages>4</tpages></addata></record>
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source MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals
subjects Animal tumors. Experimental tumors
Animals
Biological and medical sciences
Carcinoma, Transitional Cell - physiopathology
Cell Division
Cells, Cultured
Cytarabine - toxicity
Experimental renal and urinary tract tumors
Humans
Male
Medical sciences
Mice
Mice, Inbred CBA
Neoplasm Transplantation
Transplantation, Heterologous
Tumors
Urinary Bladder Neoplasms - physiopathology
Whole-Body Irradiation
title Comparison of growth of human bladder cancer in tissue culture or as xenografts with clinical and pathological characteristics
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