Targeting Claudin 18.2 Using a Highly Specific Antibody Enables Cancer Diagnosis and Guided Surgery

被引:27
作者
Zhao, Chuanke [1 ]
Rong, Zhuona [1 ]
Ding, Jin [2 ]
Wang, Lixin [1 ]
Wang, Bing [1 ,3 ]
Ding, Lei [1 ]
Meng, Lin [1 ]
Meng, Xiangxi [2 ]
Wang, Feng [2 ]
Yang, Zhi [2 ]
Shou, Chengchao [1 ]
Zhu, Hua [2 ]
机构
[1] Peking Univ Canc Hosp & Inst, Dept Biochem & Mol Biol, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing, Beijing 100142, Peoples R China
[2] Peking Univ Canc Hosp & Inst, Dept Nucl Med, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing,NMPA Key Lab Res & Evaluat Rad, Beijing 100142, Peoples R China
[3] Peking Univ Canc Hosp & Inst, Dept Ultrasound, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing, Beijing 100142, Peoples R China
基金
中国国家自然科学基金;
关键词
ESOPHAGUS;
D O I
10.1021/acs.molpharmaceut.1c00947
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
ABSTRACT: Claudin 18.2 (CLDN18.2) is a new potential target for cancer therapy, especially for advanced gastric cancer (AGC). A molecular targeting probe is of importance for patient stratification and therapeutic guidance. Here, we explored an antibodydependent molecular imaging strategy for specific detection and surgery guidance based on a CLDN18.2-specific antibody, 5C9. Two imaging probes, 124I-5C9 and Cy5.5-5C9, were synthesized. The specificity to CLDN18.2 being evidenced in the cellular experiments with control, the diagnostic utility was assessed by fluorescence imaging using xenograft models. A near-infrared fluorescent II imaging probe FD1080-5C9 was designed to facilitate the comprehensive surgical removal of lesions. 124I-5C9 immuno-PET imaging clearly delineated subcutaneous CLDN18.2positive tumors, with a peak uptake (maximum standardized uptake value; SUVmax) of 2.25 +/- 0.30, whereas the highest values for the 124I-IgG and blocking groups were 0.70 +/- 0.13 and 0.66 +/- 0.12, respectively. Cy5.5-5C9 fluorescence imaging showed similar results. As proof of the diagnosis and guided surgery (DGS) concept, 124I-5C9 and FD1080-5C9 were simultaneously administered in orthotopic CLDN18.2-positive tumor models, facilitating the comprehensive resection of tumor tissue. Combined, 124I-5C9 and FD1080-5C9 are both promising DGS tools: the former reveals CLDN18.2 in lesions as a PET probe, and the latter can guide surgery. These results provide a utility molecular imaging strategy for specific detection and surgery guidance based on a CLDN18.2specific antibody both in AGC and other cancers. KEYWORDS: CLDN18.2, molecular imaging, immuno-PET, diagnosis and guiding therapy, near-infrared fluorescent II
引用
收藏
页码:3530 / 3541
页数:12
相关论文
共 20 条
[1]   Phase III, randomised trial of avelumab versus physician's choice of chemotherapy as third-line treatment of patients with advanced gastric or gastro-oesophageal junction cancer: primary analysis of JAVELIN Gastric 300 [J].
Bang, Y. -J. ;
Ruiz, E. Yanez ;
Van Cutsem, E. ;
Lee, K. -W. ;
Wyrwicz, L. ;
Schenker, M. ;
Alsina, M. ;
Ryu, M. -H. ;
Chung, H. -C. ;
Evesque, L. ;
Al-Batran, S. -E. ;
Park, S. H. ;
Lichinitser, M. ;
Boku, N. ;
Moehler, M. H. ;
Hong, J. ;
Xiong, H. ;
Hallwachs, R. ;
Conti, I. ;
Taieb, J. .
ANNALS OF ONCOLOGY, 2018, 29 (10) :2052-2060
[2]   An orthotopic nude mouse model for preclinical research of gastric cardia cancer [J].
Bhargava, Sarah ;
Hotz, Birgit ;
Buhr, Heinz J. ;
Hotz, Hubert G. .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2009, 24 (01) :31-39
[3]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[4]   Expression of the potential therapeutic target claudin-18.2 is frequently decreased in gastric cancer: results from a large Caucasian cohort study [J].
Dottermusch, Matthias ;
Krueger, Sandra ;
Behrens, Hans-Michael ;
Halske, Christine ;
Roecken, Christoph .
VIRCHOWS ARCHIV, 2019, 475 (05) :563-571
[5]   Safety and Efficacy of Pembrolizumab Monotherapy in Patients With Previously Treated Advanced Gastric and Gastroesophageal Junction Cancer Phase 2 Clinical KEYNOTE-059 Trial [J].
Fuchs, Charles S. ;
Doi, Toshihiko ;
Jang, Raymond W. ;
Muro, Kei ;
Satoh, Taroh ;
Machado, Manuela ;
Sun, Weijing ;
Jalal, Shadia I. ;
Shah, Manish A. ;
Metges, Jean-Phillipe ;
Garrido, Marcelo ;
Golan, Talia ;
Mandala, Mario ;
Wainberg, Zev A. ;
Catenacci, Daniel V. ;
Ohtsu, Atsushi ;
Shitara, Kohei ;
Geva, Ravit ;
Bleeker, Jonathan ;
Ko, Andrew H. ;
Ku, Geoffrey ;
Philip, Philip ;
Enzinger, Peter C. ;
Bang, Yung-Jue ;
Levitan, Diane ;
Wang, Jiangdian ;
Rosales, Minori ;
Dalal, Rita P. ;
Yoon, Harry H. .
JAMA ONCOLOGY, 2018, 4 (05)
[6]   Construction of 124I-trastuzumab for noninvasive PET imaging of HER2 expression: from patient-derived xenograft models to gastric cancer patients [J].
Guo, Xiaoyi ;
Zhou, Nina ;
Chen, Zuhua ;
Liu, Teli ;
Xu, Xiaoxia ;
Lei, Xia ;
Shen, Lin ;
Gao, Jing ;
Yang, Zhi ;
Zhu, Hua .
GASTRIC CANCER, 2020, 23 (04) :614-626
[7]   Claudin18.2-Specific Chimeric Antigen Receptor Engineered T Cells for the Treatment of Gastric Cancer [J].
Jiang, Hua ;
Shi, Zhimin ;
Wang, Peng ;
Wang, Cong ;
Yang, Linlin ;
Du, Guoxiu ;
Zhang, Honghong ;
Shi, Bizhi ;
Jia, Jie ;
Li, Qixiang ;
Wang, Huamao ;
Li, Zonghai .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2019, 111 (04) :409-418
[8]   Claudin-18: a dominant tight junction protein in Barrett's esophagus and likely contributor to its acid resistance [J].
Jovov, Biljana ;
Van Itallie, Christina M. ;
Shaheen, Nicholas J. ;
Carson, Johnny L. ;
Gambling, Todd M. ;
Anderson, James M. ;
Orlando, Roy C. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2007, 293 (06) :G1106-G1113
[9]   Patient-reported outcomes from the phase II FAST trial of zolbetuximab plus EOX compared to EOX alone as first-line treatment of patients with metastatic CLDN18.2+gastroesophageal adenocarcinoma [J].
Lordick, Florian ;
Al-Batran, Salah-Eddin ;
Ganguli, Arijit ;
Morlock, Robert ;
Sahin, Ugur ;
Tuereci, Oezlem .
GASTRIC CANCER, 2021, 24 (03) :721-730
[10]   Targeted therapy for upper gastrointestinal tract cancer: current and future prospects [J].
Rosenbaum, Matthew W. ;
Gonzalez, Raul S. .
HISTOPATHOLOGY, 2021, 78 (01) :148-161