Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma

碩士 === 國立中山大學 === 生物科學系研究所 === 97 === Hepatocellular carcinoma (HCC) is one of deadliest cancers worldwide and ranking the third among all cancer-related mortalities. Current effective therapeutic approaches for HCC include surgical resection and trans-arterial embolization (TAE). Chemotherapy remai...

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Main Authors: Tian-huei Chu, 儲天輝
Other Authors: Ming-Hong Tai
Format: Others
Language:en_US
Published: 2009
Online Access:http://ndltd.ncl.edu.tw/handle/en5r5u
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spelling ndltd-TW-097NSYS51120262019-05-15T19:28:01Z http://ndltd.ncl.edu.tw/handle/en5r5u Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma Celecoxib對Novikoff原位肝癌的治療效應 Tian-huei Chu 儲天輝 碩士 國立中山大學 生物科學系研究所 97 Hepatocellular carcinoma (HCC) is one of deadliest cancers worldwide and ranking the third among all cancer-related mortalities. Current effective therapeutic approaches for HCC include surgical resection and trans-arterial embolization (TAE). Chemotherapy remains largely ineffective, and most popular used agents are epirubicin, doxorubicin, cisplatin and 5-FU. Besides, these chemotherapic drugs had potential serious side-effects such as low blood count, hair loss, vomiting, and they rarely present good anti-HCC effect in clinical practice. Our previous studies found that epirubicin injection attenuated the tumor burden of orthotopic Novikoff hepatoma, but caused serious side effects to hosts including reduction in spleen weight, white count, and body weight and high GOT level. Therefore, we aimed to evaluate possible alternative treatment such as COX-2 inhibitor for HCC. Celecoxib is a highly selective COX-2 inhibitor and less toxic than the traditional non-selective NSAIDs. Celecoxib showed relatively low cytotoxicity in Novikoff N1-S1 hepatoma cells and Clone 9 normal hepatocytes with an IC50 of up to 100 microM. Expression analysis revealed that COX-2 expression is very low in N1-S1 cells at protein and mRNA levels. Thus, N1-S1 is a kind of hepatoma cell line with low COX-II level. Interestingly, celecoxib upregulated PTEN expression and decreased AKT phosphorylation in vitro by COX-2 independent pathway, and then oral administration of celecoxib (30 mg/kg) for 7 days showed tendency of tumor suppression of Novikoff hepatoma in rats revealed by ultrasound and computed tomography (CT) scan. Histological analysis revealed that CD31-positive neo-vascularization、Ki-67-positive cell-proliferation and FOXP3-positive regulatory T cells were found to reduce in celecoxib-treated rats, and then TUNEL-positive apoptotic cells were found to increase in celecoxib-treated rats. Besides, celecoxib-treated rats exhibited no significant side effect. Therefore, oral celecoxib may be a suitable chose of adjuvant therapy in combination with epirubicin or other chemotherapeutic agents for the treatment of HCC. Ming-Hong Tai 戴明泓 2009 學位論文 ; thesis 64 en_US
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description 碩士 === 國立中山大學 === 生物科學系研究所 === 97 === Hepatocellular carcinoma (HCC) is one of deadliest cancers worldwide and ranking the third among all cancer-related mortalities. Current effective therapeutic approaches for HCC include surgical resection and trans-arterial embolization (TAE). Chemotherapy remains largely ineffective, and most popular used agents are epirubicin, doxorubicin, cisplatin and 5-FU. Besides, these chemotherapic drugs had potential serious side-effects such as low blood count, hair loss, vomiting, and they rarely present good anti-HCC effect in clinical practice. Our previous studies found that epirubicin injection attenuated the tumor burden of orthotopic Novikoff hepatoma, but caused serious side effects to hosts including reduction in spleen weight, white count, and body weight and high GOT level. Therefore, we aimed to evaluate possible alternative treatment such as COX-2 inhibitor for HCC. Celecoxib is a highly selective COX-2 inhibitor and less toxic than the traditional non-selective NSAIDs. Celecoxib showed relatively low cytotoxicity in Novikoff N1-S1 hepatoma cells and Clone 9 normal hepatocytes with an IC50 of up to 100 microM. Expression analysis revealed that COX-2 expression is very low in N1-S1 cells at protein and mRNA levels. Thus, N1-S1 is a kind of hepatoma cell line with low COX-II level. Interestingly, celecoxib upregulated PTEN expression and decreased AKT phosphorylation in vitro by COX-2 independent pathway, and then oral administration of celecoxib (30 mg/kg) for 7 days showed tendency of tumor suppression of Novikoff hepatoma in rats revealed by ultrasound and computed tomography (CT) scan. Histological analysis revealed that CD31-positive neo-vascularization、Ki-67-positive cell-proliferation and FOXP3-positive regulatory T cells were found to reduce in celecoxib-treated rats, and then TUNEL-positive apoptotic cells were found to increase in celecoxib-treated rats. Besides, celecoxib-treated rats exhibited no significant side effect. Therefore, oral celecoxib may be a suitable chose of adjuvant therapy in combination with epirubicin or other chemotherapeutic agents for the treatment of HCC.
author2 Ming-Hong Tai
author_facet Ming-Hong Tai
Tian-huei Chu
儲天輝
author Tian-huei Chu
儲天輝
spellingShingle Tian-huei Chu
儲天輝
Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma
author_sort Tian-huei Chu
title Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma
title_short Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma
title_full Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma
title_fullStr Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma
title_full_unstemmed Therapeutic Efficacy of Celecoxib for Orthotopic Novikoff Hepatoma
title_sort therapeutic efficacy of celecoxib for orthotopic novikoff hepatoma
publishDate 2009
url http://ndltd.ncl.edu.tw/handle/en5r5u
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