Prognostic impact of GPR56 in patients with colorectal cancer

Dae Ro Lim, Dong Hyun Kang, Jung Chul Kuk, Tae Hyung Kim, Eung Jin Shin, Tae Sung Ahn, Hyeong Joo Kim, Dong Jun Jeong, Moo Jun Baek, Nam Kyu Kim

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

G protein-coupled receptor 56 (GPR56) belongs to the adhesion G protein-coupled receptor subfamily, which plays a role in cell progression and survival. The aim of this study was to investigate the role of the GPR56 gene in a cell line study and the impact of its protein expression on the prognosis of colorectal cancer (CRC) patients. The effect of GPR56 on tumor cell proliferation (WST-1 assay), invasion (Transwell assay), migration (Transwell assay, wound healing assay), and colonyforming ability (semisolid agar colony-forming assay) was explored. The expression levels of GPR56 in tissue samples of 109 CRC patients were evaluated by immunohistochemistry. The prognostic value of GRP56 was analyzed using univariate and multivariate analyses. The downregulation of GPR56 in the CRC cell line reduced cell proliferation as compared with that in a control sample (48 h; p=0.042, 72 h; p=0.001). Downregulation of the GPR56 expression reduced cell invasion and migration abilities and inhibited colony-forming abilities (p<0.005). The 5-year overall survival rate was worse in the high-expression group as compared with that in the low-expression group (51.6% vs. 74.4%, p=0.008). High GPR56 expression was a significant prognostic factor for overall survival of CRC patients in the univariate (p=0.001) and multivariate (p<0.001) analyses. The expression level of GPR56 plays an important role in tumor progression in CRC, and it may serve as a prognostic indicator in CRC patients.

Original languageEnglish
Pages (from-to)580-589
Number of pages10
JournalNeoplasma
Volume68
Issue number3
DOIs
Publication statusPublished - 2021

Bibliographical note

Funding Information:
Acknowledgments: We thank the patients involved in the study and their families as they generously donated valuable tissue samples. This work was supported by the Soonchunhyang University Research Fund. This research was supported Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (grant no. 2019R1I-1A3A01061911).

Publisher Copyright:
© 2021, AEPress, s.r.o. All rights reserved.

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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