Abstract | AIM: METHODS: The CT26.WT mouse colon carcinoma cell line was grown and expanded in vitro. Following the expansion, BALB/c mice were inoculated s.c. with viable tumor cells. After the tumors had established and developed to about 80-90 mm(3), the mice were started on chemotherapy by oral administration of HE, 5-fluorouracil (5-FU) or combination. RESULTS: The antiangiogenic HE has previously been shown to inhibit the growth of melanoma in the B16F(1) tumor model in C57BL/6 mice. Our results demonstrate that mean volume of tumors in mice treated with oral HE as a single agent or in combination with 5-FU, were significantly smaller (> 60%) than those in vehicle control mice (471.2 mm(3) vs 1542.8 mm(3), P < 0.01). The significant reductions in tumor burden resulted in pronounced mean survival times (MST) and increased life spans (ILS) in the treated mice. CONCLUSION: These results indicate that HE is an effective chemotherapeutic agent for colorectal cancer in mice and that HE may be used alone or in combination with 5-FU.
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Authors | Emmanuel A Ojo-Amaize, Howard B Cottam, Olusola A Oyemade, Joseph I Okogun, Emeka J Nchekwube |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 13
Issue 34
Pg. 4586-8
(Sep 14 2007)
ISSN: 1007-9327 [Print] United States |
PMID | 17729410
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Diterpenes
- hypoestoxide
- Fluorouracil
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Topics |
- Administration, Oral
- Animals
- Antineoplastic Combined Chemotherapy Protocols
(pharmacology, therapeutic use)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Colonic Neoplasms
(drug therapy, pathology)
- Diterpenes
(administration & dosage)
- Dose-Response Relationship, Drug
- Female
- Fluorouracil
(administration & dosage)
- Mice
- Mice, Inbred BALB C
- Neoplasms, Experimental
(drug therapy, pathology)
- Time Factors
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