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- Publisher Website: 10.1016/j.ejrad.2009.04.058
- Scopus: eid_2-s2.0-77955850517
- PMID: 19481397
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Article: Evaluation of angiogenesis in colorectal carcinoma with multidetector-row CT multislice perfusion imaging
Title | Evaluation of angiogenesis in colorectal carcinoma with multidetector-row CT multislice perfusion imaging | ||||
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Authors | |||||
Keywords | Colorectal neoplasm Microvessel density Perfusion Tomography Vascular endothelial growth factor X-ray computed | ||||
Issue Date | 2010 | ||||
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/ejrad | ||||
Citation | European Journal Of Radiology, 2010, v. 75 n. 2, p. 191-196 How to Cite? | ||||
Abstract | To evaluate the correlation between 64 multidetector-row CT (64MDCT) perfusion imaging in colorectal carcinoma and microvessel density (MVD) and vascular endothelial growth factor (VEGF), 64MDCT perfusion imaging was performed in 33 patients with pathologically verified colorectal carcinoma. These images were analyzed with perfusion functional software, and time-density curves (TDC) were created for the region of interest (ROI) encompassing the tumor, the target artery and vein. The individual perfusion maps generated indicated blood flow (BF), blood volume (BV), mean transit time (MTT), and permeability-surface area product (PS). MVD and VEGF were evaluated by immunohistochemical staining with anti-CD34 and anti-VEGF, respectively. Correlations between MVD or VEGF with CT perfusion parameters and clinicopathological factors (Dukes' stages, invasion depth, and lymph node and liver metastasis) were also investigated. MVD in the colorectal carcinoma was 22.61±9.01 per ×200 field. The scores obtained for VEGF expression were 4.15±1.09. VEGF staining was positive in 25 of 29 tumors (86.2%). There was no significant correlation between the presence of MVD, VEGF expression and clinicopathological factors (P > 0.05). There was also no correlation between MVD, VEGF expression, and any dynamic CT parameters (P > 0.05). The BV and MTT were significantly higher in tumors demonstrating serous coat invasion than in those without it (t =-2.63,-2.24, P = 0.0137, 0.0331, respectively). BVwas also significantly correlated with tumor size (r = 0.41, P = 0.02). Neither BF nor PS was correlated with clinicopathological factors. In conclusion, 64MDCT perfusion imaging, MVD, and VEGF may reflect angiogenic activity, but no significant correlation among these factors © 2009 Elsevier Ireland Ltd. | ||||
Persistent Identifier | http://hdl.handle.net/10722/58639 | ||||
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.976 | ||||
ISI Accession Number ID |
Funding Information: This research is supported by the First Affiliated Hospital of SunYat-sen University. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Feng, ST | en_HK |
dc.contributor.author | Sun, CH | en_HK |
dc.contributor.author | Li, ZP | en_HK |
dc.contributor.author | Mak, HKF | en_HK |
dc.contributor.author | Peng, ZP | en_HK |
dc.contributor.author | Guo, HY | en_HK |
dc.contributor.author | Meng, QF | en_HK |
dc.date.accessioned | 2010-05-31T03:34:08Z | - |
dc.date.available | 2010-05-31T03:34:08Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | European Journal Of Radiology, 2010, v. 75 n. 2, p. 191-196 | en_HK |
dc.identifier.issn | 0720-048X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/58639 | - |
dc.description.abstract | To evaluate the correlation between 64 multidetector-row CT (64MDCT) perfusion imaging in colorectal carcinoma and microvessel density (MVD) and vascular endothelial growth factor (VEGF), 64MDCT perfusion imaging was performed in 33 patients with pathologically verified colorectal carcinoma. These images were analyzed with perfusion functional software, and time-density curves (TDC) were created for the region of interest (ROI) encompassing the tumor, the target artery and vein. The individual perfusion maps generated indicated blood flow (BF), blood volume (BV), mean transit time (MTT), and permeability-surface area product (PS). MVD and VEGF were evaluated by immunohistochemical staining with anti-CD34 and anti-VEGF, respectively. Correlations between MVD or VEGF with CT perfusion parameters and clinicopathological factors (Dukes' stages, invasion depth, and lymph node and liver metastasis) were also investigated. MVD in the colorectal carcinoma was 22.61±9.01 per ×200 field. The scores obtained for VEGF expression were 4.15±1.09. VEGF staining was positive in 25 of 29 tumors (86.2%). There was no significant correlation between the presence of MVD, VEGF expression and clinicopathological factors (P > 0.05). There was also no correlation between MVD, VEGF expression, and any dynamic CT parameters (P > 0.05). The BV and MTT were significantly higher in tumors demonstrating serous coat invasion than in those without it (t =-2.63,-2.24, P = 0.0137, 0.0331, respectively). BVwas also significantly correlated with tumor size (r = 0.41, P = 0.02). Neither BF nor PS was correlated with clinicopathological factors. In conclusion, 64MDCT perfusion imaging, MVD, and VEGF may reflect angiogenic activity, but no significant correlation among these factors © 2009 Elsevier Ireland Ltd. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/ejrad | en_HK |
dc.relation.ispartof | European Journal of Radiology | en_HK |
dc.subject | Colorectal neoplasm | - |
dc.subject | Microvessel density | - |
dc.subject | Perfusion | - |
dc.subject | Tomography | - |
dc.subject | Vascular endothelial growth factor | - |
dc.subject | X-ray computed | - |
dc.subject.mesh | Adenocarcinoma - blood supply - metabolism - radiography | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Blood Flow Velocity | en_HK |
dc.subject.mesh | Blood Volume | en_HK |
dc.subject.mesh | Colorectal Neoplasms - blood supply - metabolism - radiography | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunohistochemistry | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Microvessels - pathology | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Neovascularization, Pathologic - radiography | en_HK |
dc.subject.mesh | Perfusion Imaging | en_HK |
dc.subject.mesh | Tomography, X-Ray Computed | en_HK |
dc.subject.mesh | Vascular Endothelial Growth Factor A - metabolism | en_HK |
dc.subject.mesh | Young Adult | en_HK |
dc.title | Evaluation of angiogenesis in colorectal carcinoma with multidetector-row CT multislice perfusion imaging | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Mak, HKF:makkf@hkucc.hku.hk | en_HK |
dc.identifier.authority | Mak, HKF=rp00533 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.ejrad.2009.04.058 | en_HK |
dc.identifier.pmid | 19481397 | - |
dc.identifier.scopus | eid_2-s2.0-77955850517 | en_HK |
dc.identifier.hkuros | 165190 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77955850517&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 75 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 191 | en_HK |
dc.identifier.epage | 196 | en_HK |
dc.identifier.isi | WOS:000281484400013 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Feng, ST=15022257300 | en_HK |
dc.identifier.scopusauthorid | Sun, CH=8617235400 | en_HK |
dc.identifier.scopusauthorid | Li, ZP=23970816200 | en_HK |
dc.identifier.scopusauthorid | Mak, HKF=7004699149 | en_HK |
dc.identifier.scopusauthorid | Peng, ZP=15059373200 | en_HK |
dc.identifier.scopusauthorid | Guo, HY=34067606600 | en_HK |
dc.identifier.scopusauthorid | Meng, QF=8314601200 | en_HK |
dc.identifier.citeulike | 5022861 | - |
dc.identifier.issnl | 0720-048X | - |