PURPOSE: Angiogenesis is an indispensable process during tumor development. The currently accepted standard method for quantifying tumor angiogenesis is to assess microvessel density (MVD) based on CD105 staining, which is an independent prognostic factor for survival in patients with most solid tumor types. The goal of this study is to evaluate tumor angiogenesis in a mouse model by near-infrared fluorescence (NIRF) imaging of CD105 expression. METHODS: TRC105, a human/murine chimeric anti-CD105 monoclonal antibody, was conjugated to an NIRF dye (IRDye 800CW; Ex: 778 nm; Em: 806 nm). FACS analysis and microscopy studies were performed to compare the CD105 binding affinity of TRC105 and 800CW-TRC105. In vivo/ex vivo NIRF imaging, blocking studies, and ex vivo histology were performed on 4T1 murine breast tumor-bearing mice to evaluate the ability of 800CW-TRC105 to target tumor angiogenesis. Another chimeric antibody, cetuximab, was used as an isotype-matched control. RESULTS: FACS analysis of human umbilical vein endothelial cells (HUVECs) revealed no difference in CD105 binding affinity between TRC105 and 800CW-TRC105, which was further validated by fluorescence microscopy. 800CW conjugation of TRC105 was achieved in excellent yield (> 85%), with an average of 0.4 800CW molecules per TRC105. Serial NIRF imaging after intravenous injection of 800CW-TRC105 revealed that the 4T1 tumor could be clearly visualized as early as 30 min post-injection. Quantitative region of interest (ROI) analysis showed that the tumor uptake peaked at about 16 h post-injection. Based on ex vivo NIRF imaging at 48 h post-injection, tumor uptake of 800CW-TRC105 was higher than most organs, thus providing excellent tumor contrast. Blocking experiments, control studies with 800CW-cetuximab and 800CW, as well as ex vivo histology all confirmed the in vivo target specificity of 800CW-TRC105. CONCLUSION: This is the first successful NIRF imaging study of CD105 expression in vivo. Fast, prominent, persistent, and CD105-specific uptake of the probe during tumor angiogenesis was observed in a mouse model. 800CW-TRC105 may be used in the clinic for imaging tumor angiogenesis within the lesions close to the skin surface, tissues accessible by endoscopy, or during image-guided surgery.
PURPOSE: Angiogenesis is an indispensable process during tumor development. The currently accepted standard method for quantifying tumor angiogenesis is to assess microvessel density (MVD) based on CD105 staining, which is an independent prognostic factor for survival in patients with most solid tumor types. The goal of this study is to evaluate tumor angiogenesis in a mouse model by near-infrared fluorescence (NIRF) imaging of CD105 expression. METHODS:TRC105, a human/murine chimeric anti-CD105 monoclonal antibody, was conjugated to an NIRF dye (IRDye800CW; Ex: 778 nm; Em: 806 nm). FACS analysis and microscopy studies were performed to compare the CD105 binding affinity of TRC105 and 800CW-TRC105. In vivo/ex vivo NIRF imaging, blocking studies, and ex vivo histology were performed on 4T1 murinebreast tumor-bearing mice to evaluate the ability of 800CW-TRC105 to target tumor angiogenesis. Another chimeric antibody, cetuximab, was used as an isotype-matched control. RESULTS:FACS analysis of human umbilical vein endothelial cells (HUVECs) revealed no difference in CD105 binding affinity between TRC105 and 800CW-TRC105, which was further validated by fluorescence microscopy. 800CW conjugation of TRC105 was achieved in excellent yield (> 85%), with an average of 0.4 800CW molecules per TRC105. Serial NIRF imaging after intravenous injection of 800CW-TRC105 revealed that the 4T1 tumor could be clearly visualized as early as 30 min post-injection. Quantitative region of interest (ROI) analysis showed that the tumor uptake peaked at about 16 h post-injection. Based on ex vivo NIRF imaging at 48 h post-injection, tumor uptake of 800CW-TRC105 was higher than most organs, thus providing excellent tumor contrast. Blocking experiments, control studies with 800CW-cetuximab and 800CW, as well as ex vivo histology all confirmed the in vivo target specificity of 800CW-TRC105. CONCLUSION: This is the first successful NIRF imaging study of CD105 expression in vivo. Fast, prominent, persistent, and CD105-specific uptake of the probe during tumor angiogenesis was observed in a mouse model. 800CW-TRC105 may be used in the clinic for imaging tumor angiogenesis within the lesions close to the skin surface, tissues accessible by endoscopy, or during image-guided surgery.
Authors: Hao Hong; Yunan Yang; Yin Zhang; Jonathan W Engle; Todd E Barnhart; Robert J Nickles; Bryan R Leigh; Weibo Cai Journal: Eur J Nucl Med Mol Imaging Date: 2011-03-04 Impact factor: 9.236
Authors: Brendan Costello; Chenggang Li; Sarah Duff; David Butterworth; Ali Khan; Michael Perkins; Susan Owens; Abdul Fattah Al-Mowallad; Sarah O'Dwyer; Shant Kumar Journal: Int J Cancer Date: 2004-04-10 Impact factor: 7.396
Authors: Masanori Tsujie; Tomoko Tsujie; Hirofumi Toi; Shima Uneda; Ken Shiozaki; Hilda Tsai; Ben K Seon Journal: Int J Cancer Date: 2008-05-15 Impact factor: 7.396
Authors: Hao Hong; Yin Zhang; Jonathan W Engle; Tapas R Nayak; Charles P Theuer; Robert J Nickles; Todd E Barnhart; Weibo Cai Journal: Biomaterials Date: 2012-03-03 Impact factor: 12.479
Authors: Yin Zhang; Hao Hong; Jonathan W Engle; Yunan Yang; Charles P Theuer; Todd E Barnhart; Weibo Cai Journal: Mol Pharm Date: 2012-01-31 Impact factor: 4.939
Authors: Yin Zhang; Hao Hong; Gregory W Severin; Jonathan W Engle; Yunan Yang; Shreya Goel; Alex J Nathanson; Glenn Liu; Robert J Nickles; Bryan R Leigh; Todd E Barnhart; Weibo Cai Journal: Am J Transl Res Date: 2012-07-27 Impact factor: 4.060
Authors: Hao Hong; Gregory W Severin; Yunan Yang; Jonathan W Engle; Yin Zhang; Todd E Barnhart; Glenn Liu; Bryan R Leigh; Robert J Nickles; Weibo Cai Journal: Eur J Nucl Med Mol Imaging Date: 2011-09-10 Impact factor: 9.236
Authors: Hao Hong; Kai Yang; Yin Zhang; Jonathan W Engle; Liangzhu Feng; Yunan Yang; Tapas R Nayak; Shreya Goel; Jero Bean; Charles P Theuer; Todd E Barnhart; Zhuang Liu; Weibo Cai Journal: ACS Nano Date: 2012-02-16 Impact factor: 15.881
Authors: Hao Hong; Yin Zhang; Gregory W Severin; Yunan Yang; Jonathan W Engle; Gang Niu; Robert J Nickles; Xiaoyuan Chen; Bryan R Leigh; Todd E Barnhart; Weibo Cai Journal: Mol Pharm Date: 2012-07-19 Impact factor: 4.939
Authors: Sixiang Shi; Hakan Orbay; Yunan Yang; Stephen A Graves; Tapas R Nayak; Hao Hong; Reinier Hernandez; Haiming Luo; Shreya Goel; Charles P Theuer; Robert J Nickles; Weibo Cai Journal: J Nucl Med Date: 2015-04-16 Impact factor: 10.057
Authors: Hao Hong; Yin Zhang; Tapas R Nayak; Jonathan W Engle; Hing C Wong; Bai Liu; Todd E Barnhart; Weibo Cai Journal: J Nucl Med Date: 2012-09-17 Impact factor: 10.057