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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
Main Authors: Kuramochi, Hiroaki, Ichikawa, Tomohiko, Nihei, Naoki, Kawana, Youko, Suzuki, Hiroyoshi, Schalken, Jack A., Takeichi, Masatoshi, Nagafuchi, Akira, Ito, Haruo, Shimazaki, Jun
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container_end_page 20
container_issue 1
container_start_page 14
container_title The Prostate
container_volume 31
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
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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&lt;14::AID-PROS3&gt;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. 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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. 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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&lt;14::AID-PROS3&gt;3.0.CO;2-I</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Wiley-Blackwell Read & Publish Collection
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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