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Cited 22 time in webofscience Cited 23 time in scopus
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Imaging calreticulin for early detection of immunogenic cell death during anticancer treatmentopen access

Authors
Kim, Dong-YeonPyo, AyoungYun, MisunThangam, RamarYou, Sung-HwanZhang, YingJung, Ye-RimNguyen, Dinh-HuyVenu, AkhilKim, Hyeon SikYoon, Mee SunHong, YeongjinMin, Jung-Joon
Issue Date
Jul-2021
Publisher
Kexue Chubaneshe/Science Press
Keywords
animal imaging; calreticulin; immunogenic cell death; molecular imaging; positron emission tomography; therapy response
Citation
Journal of Nuclear Medicine, v.62, no.7, pp 956 - 960
Pages
5
Indexed
SCIE
SCOPUS
Journal Title
Journal of Nuclear Medicine
Volume
62
Number
7
Start Page
956
End Page
960
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/3506
DOI
10.2967/jnumed.120.245290
ISSN
0161-5505
1535-5667
Abstract
Surface-exposed calreticulin (ecto-CRT) is a well-known 'eat-me' signal exhibited by dying cells that contributes to their recognition and destruction by the immune system. We assessed the use of a CRT-specific binding peptide for imaging ecto-CRT during immunogenic cell death and its utility for the early prediction of treatment response. Methods: A synthetic CRT-specific peptide KLGFFKR (CRTpep) was labeled with fluorescein isothiocyanate or F-18 and characteristics of ecto-CRT was evaluated in colon cancer cell line in vitro and in vivo. Results: In vitro flow cytometry, immunofluorescence staining, and in vivo micro positron emission tomography imaging results showed that CRTpep detected pre-apoptotic cells treated with immunogenic drugs or radiation, but not those treated with the non-immunogenic drug or a non-therapeutic dose of immunogenic drug. Conclusion: The present results indicate that the CRT-specific peptide would enable the prediction of therapeutic response, thereby facilitating early decisions regarding the continuation or discontinuation of immunogenic treatment.
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