Transcatheter arterial embolization followed by octreotide and celecoxib synergistically prolongs survival of rabbits with hepatic VX2 allografts. Issue 1 (21st December 2012)
- Record Type:
- Journal Article
- Title:
- Transcatheter arterial embolization followed by octreotide and celecoxib synergistically prolongs survival of rabbits with hepatic VX2 allografts. Issue 1 (21st December 2012)
- Main Title:
- Transcatheter arterial embolization followed by octreotide and celecoxib synergistically prolongs survival of rabbits with hepatic VX2 allografts
- Authors:
- Tong, Huan
Li, Xiao
Zhang, Chun Le
Gao, Jin Hang
Wen, Shi Lei
Huang, Zhi Yin
Wen, Fu Qiang
Fu, Ping
Tang, Cheng Wei - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cdd12001-sec-0001" sec-type="section"> <title>Objective</title> <p>To validate the efficacy of an innovative multimodality therapy with transcatheter arterial embolization (TAE) plus octreotide and celecoxib in reducing neoangiogenesis and prolonging the survival of rabbits with hepatocellular carcinoma.</p> </sec> <sec id="cdd12001-sec-0002" sec-type="section"> <title>Methods</title> <p>Rabbits with hepatic VX2 allografts were divided into four groups: control group, TAE group, octreotide + celecoxib (O + C) group and the multimodality therapy (TAE + O + C) group. Survival of the rabbits was analyzed using the Kaplan–Meier method and the expression of CD31 in tumor tissues was detected by immunohistochemistry.</p> </sec> <sec id="cdd12001-sec-0003" sec-type="section"> <title>Results</title> <p>Rabbits in the TAE + O + C group lived nearly 20 days longer than those in the control group. The survival rate of the TAE + O + C group was 50% at day 80 and was the highest among the four groups (<italic>P</italic> &lt; 0.05). No VX2 allograft‐bearing rabbits in the control group lived longer than 60 days. Compared with the control group, the survival time of the other two intervention groups were not prolonged significantly (<italic>P</italic> &gt; 0.05). The CD31 expression induced by TAE was reduced significantly in TAE + O + C group (<italic>P</italic> &lt; 0.05). Less metastasis was<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cdd12001-sec-0001" sec-type="section"> <title>Objective</title> <p>To validate the efficacy of an innovative multimodality therapy with transcatheter arterial embolization (TAE) plus octreotide and celecoxib in reducing neoangiogenesis and prolonging the survival of rabbits with hepatocellular carcinoma.</p> </sec> <sec id="cdd12001-sec-0002" sec-type="section"> <title>Methods</title> <p>Rabbits with hepatic VX2 allografts were divided into four groups: control group, TAE group, octreotide + celecoxib (O + C) group and the multimodality therapy (TAE + O + C) group. Survival of the rabbits was analyzed using the Kaplan–Meier method and the expression of CD31 in tumor tissues was detected by immunohistochemistry.</p> </sec> <sec id="cdd12001-sec-0003" sec-type="section"> <title>Results</title> <p>Rabbits in the TAE + O + C group lived nearly 20 days longer than those in the control group. The survival rate of the TAE + O + C group was 50% at day 80 and was the highest among the four groups (<italic>P</italic> &lt; 0.05). No VX2 allograft‐bearing rabbits in the control group lived longer than 60 days. Compared with the control group, the survival time of the other two intervention groups were not prolonged significantly (<italic>P</italic> &gt; 0.05). The CD31 expression induced by TAE was reduced significantly in TAE + O + C group (<italic>P</italic> &lt; 0.05). Less metastasis was detected in TAE + O + C group.</p> </sec> <sec id="cdd12001-sec-0004" sec-type="section"> <title>Conclusion</title> <p>TAE followed by the long‐term administration of octreotide and celecoxib can synergistically prolong the survival of rabbits with hepatic VX2 allografts by inhibiting potential neoangiogenesis, tumor growth and metastasis.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of digestive diseases. Volume 14:Issue 1(2013:Jan.)
- Journal:
- Journal of digestive diseases
- Issue:
- Volume 14:Issue 1(2013:Jan.)
- Issue Display:
- Volume 14, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 14
- Issue:
- 1
- Issue Sort Value:
- 2013-0014-0001-0000
- Page Start:
- 29
- Page End:
- 37
- Publication Date:
- 2012-12-21
- Subjects:
- Digestive organs -- Diseases -- Periodicals
Gastroenterology -- Periodicals
616.3 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1751-2972&site=1 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1751-2980.12001 ↗
- Languages:
- English
- ISSNs:
- 1751-2972
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4969.606000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4314.xml