JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats

<p>Abstract</p> <p>Background</p> <p>Epidemiological studies have shown that individuals who regularly consume NSAIDs have lower rates of mortality associated with colorectal cancer. Because COX-2 inhibitors prevent tumor growth through some mechanisms, we assessed the...

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Main Authors: Enomoto Masayuki, Higuchi Tetsuro, Uetake Hiroyuki, Kobayashi Hirotoshi, Sugihara Kenichi
Format: Article
Language:English
Published: BMC 2005-03-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/5/26
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spelling doaj-23362673907e4981823fce27cf6fb1f82020-11-24T21:35:04ZengBMCBMC Cancer1471-24072005-03-01512610.1186/1471-2407-5-26JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in ratsEnomoto MasayukiHiguchi TetsuroUetake HiroyukiKobayashi HirotoshiSugihara Kenichi<p>Abstract</p> <p>Background</p> <p>Epidemiological studies have shown that individuals who regularly consume NSAIDs have lower rates of mortality associated with colorectal cancer. Because COX-2 inhibitors prevent tumor growth through some mechanisms, we assessed the effect of JTE-522, a selective COX-2 inhibitor, on pulmonary metastases of colon cancer in a rat model.</p> <p>Methods</p> <p>A suspension of 5 × 10<sup>6 </sup>RCN-9 (rat colon cancer cells) was injected into the tail vein of 24 anesthetized male F344/DuCrj rats. Oral JTE-522 (0, 3, 10, or 30 mg/kg/day) was administered from the day before RCN-9 injection until the end of the study. Twenty-four days later, the lungs were removed from sacrificed rats and weighed. Pulmonary metastatic tumors were microscopically evaluated in the largest cross sections. We also performed immunohistochemical staining for both COX-2 and VEGF.</p> <p>Results</p> <p>JTE-522 dose-dependently decreased lung weight (p = 0.001) and the size of pulmonary metastatic tumors (p = 0.0002). However, the differences in the number of metastatic tumors among 4 groups were insignificant. Significant adverse effects of JTE-522 were undetectable. Immunohistochemical staining showed high levels of both COX-2 and VEGF in pulmonary metastatic tumors.</p> <p>Conclusion</p> <p>JTE-522 dose-dependently decreased the size, but not the number of pulmonary metastases. COX-2 inhibitors might block metastatic tumor growth, but not actual metastasis. Selective COX-2 inhibitors might be useful as therapeutic agents that inhibit the growth of metastatic tumors, as well as the tumorigenesis of colorectal cancer.</p> http://www.biomedcentral.com/1471-2407/5/26
collection DOAJ
language English
format Article
sources DOAJ
author Enomoto Masayuki
Higuchi Tetsuro
Uetake Hiroyuki
Kobayashi Hirotoshi
Sugihara Kenichi
spellingShingle Enomoto Masayuki
Higuchi Tetsuro
Uetake Hiroyuki
Kobayashi Hirotoshi
Sugihara Kenichi
JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
BMC Cancer
author_facet Enomoto Masayuki
Higuchi Tetsuro
Uetake Hiroyuki
Kobayashi Hirotoshi
Sugihara Kenichi
author_sort Enomoto Masayuki
title JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
title_short JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
title_full JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
title_fullStr JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
title_full_unstemmed JTE-522, a selective COX-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
title_sort jte-522, a selective cox-2 inhibitor, inhibits growth of pulmonary metastases of colorectal cancer in rats
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2005-03-01
description <p>Abstract</p> <p>Background</p> <p>Epidemiological studies have shown that individuals who regularly consume NSAIDs have lower rates of mortality associated with colorectal cancer. Because COX-2 inhibitors prevent tumor growth through some mechanisms, we assessed the effect of JTE-522, a selective COX-2 inhibitor, on pulmonary metastases of colon cancer in a rat model.</p> <p>Methods</p> <p>A suspension of 5 × 10<sup>6 </sup>RCN-9 (rat colon cancer cells) was injected into the tail vein of 24 anesthetized male F344/DuCrj rats. Oral JTE-522 (0, 3, 10, or 30 mg/kg/day) was administered from the day before RCN-9 injection until the end of the study. Twenty-four days later, the lungs were removed from sacrificed rats and weighed. Pulmonary metastatic tumors were microscopically evaluated in the largest cross sections. We also performed immunohistochemical staining for both COX-2 and VEGF.</p> <p>Results</p> <p>JTE-522 dose-dependently decreased lung weight (p = 0.001) and the size of pulmonary metastatic tumors (p = 0.0002). However, the differences in the number of metastatic tumors among 4 groups were insignificant. Significant adverse effects of JTE-522 were undetectable. Immunohistochemical staining showed high levels of both COX-2 and VEGF in pulmonary metastatic tumors.</p> <p>Conclusion</p> <p>JTE-522 dose-dependently decreased the size, but not the number of pulmonary metastases. COX-2 inhibitors might block metastatic tumor growth, but not actual metastasis. Selective COX-2 inhibitors might be useful as therapeutic agents that inhibit the growth of metastatic tumors, as well as the tumorigenesis of colorectal cancer.</p>
url http://www.biomedcentral.com/1471-2407/5/26
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