Abstract | INTRODUCTION: METHODS: This study investigated CCK2R expression in a wide range of cell lines and clinical CRC samples, and explored expression pattern and prognostic value of CCK2R in relation to clinicopathological parameters. The location and expression levels of CCK2R were measured by immunocytochemical (ICC), qRT-PCR and Western blot. The druggability and antineoplastic effects of CCK2R as a therapeutic target were investigated using an anti-CCK2R targeting recombinant toxin named rCCK8PE38 by CCK-8 assay. RESULTS: Compared with paracarcinoma tissues, tumor samples showed overexpression of CCK2R (p = 0.028) including both CRC tissue and plasma samples, with plasma detection showing a significant indication for CCK2R evaluation. Aberrant expression correlated significantly with histological type (p = 0.032) and p53 status (p < 0.01), and patients with CCK2R overexpression had significantly lower disease-free survival. Application of rCCK8PE38 demonstrated the specificity and druggability of CCK2R as a therapeutic target, providing a strategy for clinical case screening of drugs targeting CCK2R. CONCLUSION: This study highlighted the aberrant expression and clinical correlation of CCK2R and reveals its diagnostic, prognostic and treatment value in CRC. We hypothesize that CCK2R serve as a target for the diagnosis and treatment of this cancer.
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Authors | Jiang Chang, Zeng-Shan Liu, De-Feng Song, Meng Li, Song Zhang, Ke Zhao, Yu-Ting Guan, Hong-Lin Ren, Yan-Song Li, Yu Zhou, Xi-Lin Liu, Shi-Ying Lu, Pan Hu |
Journal | Journal of cancer research and clinical oncology
(J Cancer Res Clin Oncol)
Vol. 146
Issue 9
Pg. 2205-2217
(Sep 2020)
ISSN: 1432-1335 [Electronic] Germany |
PMID | 32488497
(Publication Type: Journal Article)
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Chemical References |
- Receptor, Cholecystokinin B
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Topics |
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Cell Line, Tumor
- Colorectal Neoplasms
(genetics, pathology)
- Disease-Free Survival
- Female
- Gene Expression Regulation, Neoplastic
(genetics)
- HCT116 Cells
- HT29 Cells
- Hep G2 Cells
- Humans
- Male
- Middle Aged
- Prognosis
- Receptor, Cholecystokinin B
(genetics)
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