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Suppression of invasive ability of highly metastatic rat prostate cancer by introduction of human chromosome 8
BACKGROUND Introduction of human chromosome 8 to a highly metastatic subline (AT6.2) from the Dunning R‐3327 rat prostate cancer resulted in suppression of metastatic ability of the resultant microcell hybrids (AT6.2–8 clones) [12]. The present study has been performed to clarify which step of metas...
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Published in: | The Prostate 1997-04, Vol.31 (1), p.14-20 |
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container_title | The Prostate |
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creator | Kuramochi, Hiroaki Ichikawa, Tomohiko Nihei, Naoki Kawana, Youko Suzuki, Hiroyoshi Schalken, Jack A. Takeichi, Masatoshi Nagafuchi, Akira Ito, Haruo Shimazaki, Jun |
description | BACKGROUND
Introduction of human chromosome 8 to a highly metastatic subline (AT6.2) from the Dunning R‐3327 rat prostate cancer resulted in suppression of metastatic ability of the resultant microcell hybrids (AT6.2–8 clones) [12]. The present study has been performed to clarify which step of metastasis was suppressed in the microcell hybrids.
METHODS
Northern blot analysis of E‐cadherin and alpha‐catenin, in vitro invasion assay, and intra‐venous metastasis assay by injection of tumor cells into the lateral tail vein of nude mice were performed.
RESULTS
No detectable expressions of either E‐cadherin or alpha‐catenin were found in either AT6.2 parental or AT6.2–8 microcell hybrid clones. In the invasion assay, invasiveness of AT6.2–8 hybrid clones was less than that of the AT6.2 parental clone. In the intravenous metastasis assay, no significant differences in the number of lung metastases were observed among these cell lines.
CONCLUSIONS
Introduction of human chromosome 8 to AT6.2 cells shows suppression of invasiveness and no suppression of cell dissociation or process after entry into blood circulation. This suggests that human chromosome 8 contains suppressor gene(s) for the invasive ability of prostate cancer. Prostate 31:14–20, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-0045(19970401)31:1<14::AID-PROS3>3.0.CO;2-I |
format | article |
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Introduction of human chromosome 8 to a highly metastatic subline (AT6.2) from the Dunning R‐3327 rat prostate cancer resulted in suppression of metastatic ability of the resultant microcell hybrids (AT6.2–8 clones) [12]. The present study has been performed to clarify which step of metastasis was suppressed in the microcell hybrids.
METHODS
Northern blot analysis of E‐cadherin and alpha‐catenin, in vitro invasion assay, and intra‐venous metastasis assay by injection of tumor cells into the lateral tail vein of nude mice were performed.
RESULTS
No detectable expressions of either E‐cadherin or alpha‐catenin were found in either AT6.2 parental or AT6.2–8 microcell hybrid clones. In the invasion assay, invasiveness of AT6.2–8 hybrid clones was less than that of the AT6.2 parental clone. In the intravenous metastasis assay, no significant differences in the number of lung metastases were observed among these cell lines.
CONCLUSIONS
Introduction of human chromosome 8 to AT6.2 cells shows suppression of invasiveness and no suppression of cell dissociation or process after entry into blood circulation. This suggests that human chromosome 8 contains suppressor gene(s) for the invasive ability of prostate cancer. Prostate 31:14–20, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/(SICI)1097-0045(19970401)31:1<14::AID-PROS3>3.0.CO;2-I</identifier><identifier>PMID: 9108881</identifier><identifier>CODEN: PRSTDS</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>alpha Catenin ; Animal tumors. Experimental tumors ; Animals ; Biological and medical sciences ; Cadherins - metabolism ; Chromosomes, Human, Pair 8 ; Collagen ; Cytoskeletal Proteins - metabolism ; Drug Combinations ; Experimental renal and urinary tract tumors ; human chromosome 8 ; Humans ; invasion ; Laminin ; Lung Neoplasms - secondary ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Neoplasm Invasiveness - genetics ; Neoplasm Proteins - metabolism ; Neoplasm Transplantation ; prostate cancer ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; Proteoglycans ; Rats ; suppression of metastasis ; Transfection ; Tumor Cells, Cultured ; Tumors</subject><ispartof>The Prostate, 1997-04, Vol.31 (1), p.14-20</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5103-f91e814a08096994e48e784fd05e62bf49de0abcfac831f822b5ee7e59de157f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2651354$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9108881$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuramochi, Hiroaki</creatorcontrib><creatorcontrib>Ichikawa, Tomohiko</creatorcontrib><creatorcontrib>Nihei, Naoki</creatorcontrib><creatorcontrib>Kawana, Youko</creatorcontrib><creatorcontrib>Suzuki, Hiroyoshi</creatorcontrib><creatorcontrib>Schalken, Jack A.</creatorcontrib><creatorcontrib>Takeichi, Masatoshi</creatorcontrib><creatorcontrib>Nagafuchi, Akira</creatorcontrib><creatorcontrib>Ito, Haruo</creatorcontrib><creatorcontrib>Shimazaki, Jun</creatorcontrib><title>Suppression of invasive ability of highly metastatic rat prostate cancer by introduction of human chromosome 8</title><title>The Prostate</title><addtitle>Prostate</addtitle><description>BACKGROUND
Introduction of human chromosome 8 to a highly metastatic subline (AT6.2) from the Dunning R‐3327 rat prostate cancer resulted in suppression of metastatic ability of the resultant microcell hybrids (AT6.2–8 clones) [12]. The present study has been performed to clarify which step of metastasis was suppressed in the microcell hybrids.
METHODS
Northern blot analysis of E‐cadherin and alpha‐catenin, in vitro invasion assay, and intra‐venous metastasis assay by injection of tumor cells into the lateral tail vein of nude mice were performed.
RESULTS
No detectable expressions of either E‐cadherin or alpha‐catenin were found in either AT6.2 parental or AT6.2–8 microcell hybrid clones. In the invasion assay, invasiveness of AT6.2–8 hybrid clones was less than that of the AT6.2 parental clone. In the intravenous metastasis assay, no significant differences in the number of lung metastases were observed among these cell lines.
CONCLUSIONS
Introduction of human chromosome 8 to AT6.2 cells shows suppression of invasiveness and no suppression of cell dissociation or process after entry into blood circulation. This suggests that human chromosome 8 contains suppressor gene(s) for the invasive ability of prostate cancer. Prostate 31:14–20, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>alpha Catenin</subject><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cadherins - metabolism</subject><subject>Chromosomes, Human, Pair 8</subject><subject>Collagen</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Drug Combinations</subject><subject>Experimental renal and urinary tract tumors</subject><subject>human chromosome 8</subject><subject>Humans</subject><subject>invasion</subject><subject>Laminin</subject><subject>Lung Neoplasms - secondary</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Neoplasm Invasiveness - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Neoplasm Transplantation</subject><subject>prostate cancer</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Proteoglycans</subject><subject>Rats</subject><subject>suppression of metastasis</subject><subject>Transfection</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>0270-4137</issn><issn>1097-0045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkU-P0zAQxSMEWsrCR0DKAaHdQ8o4dhqnoJVWKSwRK4q2wB5HjjuhhvwpdrLQb49DSy8gIR8szzz__DwvCC4YTBlA_OJsVeTFOYMsjQBEcsayLAUB7JyzOXvFxHx-WSyiDzfLFb_gU5jmy5dxVNwLJscr94MJxClEgvH0YfDIua8AHg3xSXCSMZBSsknQrobt1pJzpmvDrgpNe6ecuaNQlaY2_W6sbcyXTb0LG-qV61VvdGhVH25tN54o1KrVZMNy5y_3tlsPuj_ANkOj2lBvbNd0rmsolI-DB5WqHT057KfBpzevP-Zvo-vlVZFfXkc6YcCjKmMkmVAgIZtlmSAhKZWiWkNCs7isRLYmUKWulJacVTKOy4QopcTXWZJW_DR4vud6l98Hcj02xmmqa9VSNzhMZcalTBMv_LwXav8dZ6nCrTWNsjtkgGMQiGMQOE4Vx6ninyCQM_RLIPog8HcQyBEwX2KMhQc_PTgYyobWR-xh8r7_7NBXTqu6sn6Kxh1l8SxhPBFedruX_TA17f4y9z9v_7K2L3hytCcb19PPI1nZbzhLeZrg7fsrXMC7xc3KP7TgvwD1DsG6</recordid><startdate>19970401</startdate><enddate>19970401</enddate><creator>Kuramochi, Hiroaki</creator><creator>Ichikawa, Tomohiko</creator><creator>Nihei, Naoki</creator><creator>Kawana, Youko</creator><creator>Suzuki, Hiroyoshi</creator><creator>Schalken, Jack A.</creator><creator>Takeichi, Masatoshi</creator><creator>Nagafuchi, Akira</creator><creator>Ito, Haruo</creator><creator>Shimazaki, Jun</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19970401</creationdate><title>Suppression of invasive ability of highly metastatic rat prostate cancer by introduction of human chromosome 8</title><author>Kuramochi, Hiroaki ; Ichikawa, Tomohiko ; Nihei, Naoki ; Kawana, Youko ; Suzuki, Hiroyoshi ; Schalken, Jack A. ; Takeichi, Masatoshi ; Nagafuchi, Akira ; Ito, Haruo ; Shimazaki, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5103-f91e814a08096994e48e784fd05e62bf49de0abcfac831f822b5ee7e59de157f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>alpha Catenin</topic><topic>Animal tumors. Experimental tumors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cadherins - metabolism</topic><topic>Chromosomes, Human, Pair 8</topic><topic>Collagen</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Drug Combinations</topic><topic>Experimental renal and urinary tract tumors</topic><topic>human chromosome 8</topic><topic>Humans</topic><topic>invasion</topic><topic>Laminin</topic><topic>Lung Neoplasms - secondary</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Neoplasm Invasiveness - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Neoplasm Transplantation</topic><topic>prostate cancer</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Proteoglycans</topic><topic>Rats</topic><topic>suppression of metastasis</topic><topic>Transfection</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuramochi, Hiroaki</creatorcontrib><creatorcontrib>Ichikawa, Tomohiko</creatorcontrib><creatorcontrib>Nihei, Naoki</creatorcontrib><creatorcontrib>Kawana, Youko</creatorcontrib><creatorcontrib>Suzuki, Hiroyoshi</creatorcontrib><creatorcontrib>Schalken, Jack A.</creatorcontrib><creatorcontrib>Takeichi, Masatoshi</creatorcontrib><creatorcontrib>Nagafuchi, Akira</creatorcontrib><creatorcontrib>Ito, Haruo</creatorcontrib><creatorcontrib>Shimazaki, Jun</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Prostate</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuramochi, Hiroaki</au><au>Ichikawa, Tomohiko</au><au>Nihei, Naoki</au><au>Kawana, Youko</au><au>Suzuki, Hiroyoshi</au><au>Schalken, Jack A.</au><au>Takeichi, Masatoshi</au><au>Nagafuchi, Akira</au><au>Ito, Haruo</au><au>Shimazaki, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppression of invasive ability of highly metastatic rat prostate cancer by introduction of human chromosome 8</atitle><jtitle>The Prostate</jtitle><addtitle>Prostate</addtitle><date>1997-04-01</date><risdate>1997</risdate><volume>31</volume><issue>1</issue><spage>14</spage><epage>20</epage><pages>14-20</pages><issn>0270-4137</issn><eissn>1097-0045</eissn><coden>PRSTDS</coden><abstract>BACKGROUND
Introduction of human chromosome 8 to a highly metastatic subline (AT6.2) from the Dunning R‐3327 rat prostate cancer resulted in suppression of metastatic ability of the resultant microcell hybrids (AT6.2–8 clones) [12]. The present study has been performed to clarify which step of metastasis was suppressed in the microcell hybrids.
METHODS
Northern blot analysis of E‐cadherin and alpha‐catenin, in vitro invasion assay, and intra‐venous metastasis assay by injection of tumor cells into the lateral tail vein of nude mice were performed.
RESULTS
No detectable expressions of either E‐cadherin or alpha‐catenin were found in either AT6.2 parental or AT6.2–8 microcell hybrid clones. In the invasion assay, invasiveness of AT6.2–8 hybrid clones was less than that of the AT6.2 parental clone. In the intravenous metastasis assay, no significant differences in the number of lung metastases were observed among these cell lines.
CONCLUSIONS
Introduction of human chromosome 8 to AT6.2 cells shows suppression of invasiveness and no suppression of cell dissociation or process after entry into blood circulation. This suggests that human chromosome 8 contains suppressor gene(s) for the invasive ability of prostate cancer. Prostate 31:14–20, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9108881</pmid><doi>10.1002/(SICI)1097-0045(19970401)31:1<14::AID-PROS3>3.0.CO;2-I</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alpha Catenin Animal tumors. Experimental tumors Animals Biological and medical sciences Cadherins - metabolism Chromosomes, Human, Pair 8 Collagen Cytoskeletal Proteins - metabolism Drug Combinations Experimental renal and urinary tract tumors human chromosome 8 Humans invasion Laminin Lung Neoplasms - secondary Male Medical sciences Mice Mice, Inbred BALB C Mice, Nude Neoplasm Invasiveness - genetics Neoplasm Proteins - metabolism Neoplasm Transplantation prostate cancer Prostatic Neoplasms - genetics Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology Proteoglycans Rats suppression of metastasis Transfection Tumor Cells, Cultured Tumors |
title | Suppression of invasive ability of highly metastatic rat prostate cancer by introduction of human chromosome 8 |
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