18 F-labelled annexin V: a PET tracer for apoptosis imaging

2004 ◽  
Vol 31 (4) ◽  
pp. 469-474 ◽  
Author(s):  
Yoshihiro Murakami ◽  
Hiroyuki Takamatsu ◽  
Junichi Taki ◽  
Mitsuyoshi Tatsumi ◽  
Akihiro Noda ◽  
...  
2013 ◽  
Vol 298 (3) ◽  
pp. 1733-1738 ◽  
Author(s):  
Jian-Cheng Zhu ◽  
Feng Wang ◽  
Wei Fang ◽  
Zi-Chun Hua ◽  
Zi-zheng Wang

2020 ◽  
Vol 7 (24) ◽  
pp. 2070137
Author(s):  
Hyunjin Kim ◽  
Hee Yeon Kim ◽  
Eun Young Lee ◽  
Boem Kyu Choi ◽  
Hyonchol Jang ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Kazuma Ogawa ◽  
Miho Aoki

Since apoptosis plays an important role in maintaining homeostasis and is associated with responses to therapy, molecular imaging of apoptotic cells could be useful for early detection of therapeutic effects, particularly in oncology. Radiolabeled annexin V compounds are the hallmark in apoptosis imagingin vivo. These compounds are reviewed from the genesis of apoptosis (cell death) imaging agents up to recent years. They have some disadvantages, including slow clearance and immunogenicity, because they are protein-based imaging agents. For this reason, several studies have been conducted in recent years to develop low molecule apoptosis imaging agents. In this review, radiolabeled phosphatidylserine targeted peptides, radiolabeled bis(zinc(II)-dipicolylamine) complex, radiolabeled 5-fluoropentyl-2-methyl-malonic acid (ML-10), caspase-3 activity imaging agents, radiolabeled duramycin, and radiolabeled phosphonium cation are reviewed as promising low-molecular-weight apoptosis imaging agents.


2021 ◽  
Vol 2021 ◽  
pp. 1-11
Author(s):  
Jasmin Gross ◽  
Karin Palmowski ◽  
Dennis Doleschel ◽  
Anne Rix ◽  
Felix Gremse ◽  
...  

Aim of the Study. To compare Annexin V-based optical apoptosis imaging with the assessment of the glucose metabolism using 18F-FDG-PET/CT for monitoring the response to cytotoxic (carboplatin) and anti-angiogenic (sunitinib) therapy. Methods. For apoptosis imaging, the near-infrared probe Annexin Vivo750 was used in combination with fluorescence molecular tomography and microcomputed tomography (FMT/µCT). Glucose metabolism was assessed using 18F-FDG-PET/CT. Five groups of nude mice bearing lung cancer xenografts (A549) were investigated: (i) untreated controls and two groups after (ii) cytotoxic (carboplatin) or (iii) anti-angiogenic (sunitinib) treatment for four and nine days, respectively. Imaging data were validated by immunohistochemistry. Results. In response to carboplatin treatment, an inverse relation was found between the change in glucose metabolism and apoptosis in A549 tumors. Annexin Vivo showed a continually increasing tumor accumulation, while the tumor-to-muscle ratio of 18F-FDG continuously decreased during therapy. Immunohistochemistry revealed a significantly higher tumor apoptosis ( p = 0.007 ) and a minor but not significant reduction in vessel density only at day 9 of carboplatin therapy. Interestingly, during anti-angiogenic treatment there was an early drop in the tumor-to-muscle ratio between days 0 and 4, followed by a subsequent minor decrease (18F-FDG tumor-to-muscle-ratio: 1.9 ± 0.4; day 4: 1.1 ± 0.2; day 9: 1.0 ± 0.2; p = 0.021 and p = 0.001 , respectively). The accumulation of Annexin Vivo continuously increased over time (Annexin Vivo: untreated: 53.7 ± 36.4 nM; day 4: 87.2 ± 53.4 nM; day 9: 115.1 ± 103.7 nM) but failed to display the very prominent early induction of tumor apoptosis that was found by histology already at day 4 (TUNEL: p = 0.0036 ) together with a decline in vessel density (CD31: p = 0.004 ), followed by no significant changes thereafter. Conclusion. Both molecular imaging approaches enable visualizing the effects of cytotoxic and anti-angiogenic therapy in A549 tumors. However, the early and strong tumor apoptosis induced by the anti-angiogenic agent sunitinib was more sensitively and reliably captured by monitoring of the glucose metabolism as compared to Annexin V-based apoptosis imaging.


2008 ◽  
Vol 19 (8) ◽  
pp. 1684-1688 ◽  
Author(s):  
Xuehe Li ◽  
Jeanne M. Link ◽  
Svetlana Stekhova ◽  
Kevin J. Yagle ◽  
Christina Smith ◽  
...  

2010 ◽  
Vol 51 (11) ◽  
pp. 1659-1662 ◽  
Author(s):  
G. Niu ◽  
X. Chen
Keyword(s):  

2016 ◽  
Vol 310 (1) ◽  
pp. 413-421 ◽  
Author(s):  
Sepideh Khoshbakht ◽  
Davood Beiki ◽  
Parham Geramifar ◽  
Farzad Kobarfard ◽  
Omid Sabzevari ◽  
...  
Keyword(s):  

Oncotarget ◽  
2017 ◽  
Vol 8 (31) ◽  
pp. 51086-51095 ◽  
Author(s):  
Chunxiong Lu ◽  
Quanfu Jiang ◽  
Minjin Hu ◽  
Cheng Tan ◽  
Huixin Yu ◽  
...  

Author(s):  
Y. L. Chen ◽  
C. C. Wu ◽  
Y. C. Lin ◽  
Y. H. Pan ◽  
T. W. Lee ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document