Imaging calreticulin for early detection of immunogenic cell death during anticancer treatmentopen access
- Authors
- Kim, Dong-Yeon; Pyo, Ayoung; Yun, Misun; Thangam, Ramar; You, Sung-Hwan; Zhang, Ying; Jung, Ye-Rim; Nguyen, Dinh-Huy; Venu, Akhil; Kim, Hyeon Sik; Yoon, Mee Sun; Hong, Yeongjin; Min, 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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