Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9964
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dc.contributor.authorDaruwalla, Jurstineen
dc.contributor.authorNikfarjam, Mehrdaden
dc.contributor.authorMalcontenti-Wilson, Caterinaen
dc.contributor.authorMuralidharan, Vijayaragavanen
dc.contributor.authorChristophi, Christopheren
dc.date.accessioned2015-05-15T23:15:45Z
dc.date.available2015-05-15T23:15:45Z
dc.date.issued2005-08-01en
dc.identifier.citationJournal of Surgical Oncology; 91(2): 134-40en
dc.identifier.govdoc16028287en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9964en
dc.description.abstractThalidomide has undergone resurgence in the treatment of specific malignancies. One of the possible actions of thalidomide may be an antiangiogenic effect. This study investigates the effects of thalidomide on tumor growth and long-term survival in a murine model of colorectal liver metastases.Liver metastases were produced in male CBA mice by intrasplenic injection of a dimethyl hydrazine induced MoCR colon cancer murine cell line. Thalidomide was administered daily at doses ranging from 50 to 300 mg/kg by intraperitoneal injection. Tumor growth was assessed using quantitative stereological analysis. The effect on long-term survival was determined at the maximum tolerated dose using Kaplan-Meier analysis. The microvascular effects of thalidomide were assessed by laser Doppler flowmetry (LDF) and microvascular resin casting. Immunohistochemistry was used to determine vascular endothelial growth factor (VGEF) and basic fibroblast growth factor (bFGF) expression.Thalidomide, (50-300 mg/kg) caused no significant reduction in tumor growth by day 21 following induction of liver metastases and caused systemic toxicity at a dose of 300 mg/kg. At a dose of 200 mg/kg given beyond 35 days, thalidomide significantly reduced tumor growth compared to control, (P = 0.029). No significant impact on survival was however observed (P = 0.93). LDF and microvascular resin casting showed no differences in blood flow or tumor microvascular architecture. VGEF and FGF were expressed in tumors, but remained unaltered by thalidomide administration compared to matched controls.Thalidomide caused a significant reduction in the volume of colorectal liver metastases during the late phase of tumor growth. There was however no improvement in survival. Tumor growth reduction in this model did not appear to be due to microvascular changes or altered expression of VGEF or basic FGF. Further investigation into potential mechanisms of action of thalidomide and its synergistic use with other therapies is required.en
dc.language.isoenen
dc.subject.otherAnalysis of Varianceen
dc.subject.otherAngiogenesis Inhibitors.administration & dosage.pharmacologyen
dc.subject.otherAnimalsen
dc.subject.otherColorectal Neoplasms.blood supply.metabolism.pathologyen
dc.subject.otherFibroblast Growth Factor 2.biosynthesisen
dc.subject.otherImmunohistochemistryen
dc.subject.otherLaser-Doppler Flowmetryen
dc.subject.otherLiver Neoplasms.secondaryen
dc.subject.otherMaleen
dc.subject.otherMiceen
dc.subject.otherMice, Inbred CBAen
dc.subject.otherNeoplasm Transplantationen
dc.subject.otherNeovascularization, Pathologic.pathologyen
dc.subject.otherThalidomide.administration & dosage.pharmacologyen
dc.subject.otherVascular Endothelial Growth Factor A.biosynthesisen
dc.titleEffect of thalidomide on colorectal cancer liver metastases in CBA mice.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of surgical oncologyen
dc.identifier.affiliationThe University of Melbourne, Department of Surgery, Austin Health Hospital, Studley Road, Heidelberg, Australiaen
dc.identifier.doi10.1002/jso.20289en
dc.description.pages134-40en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/16028287en
dc.type.austinJournal Articleen
local.name.researcherChristophi, Christopher
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptSurgery (University of Melbourne)-
crisitem.author.deptSurgery (University of Melbourne)-
crisitem.author.deptHepatopancreatobiliary Surgery-
crisitem.author.deptSurgery-
crisitem.author.deptSurgery-
crisitem.author.deptHepatopancreatobiliary Surgery-
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