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Clinical significance of reduced GPRC5A expression in surgically resected non-small cell lung cancer.

Authors
  • Jin, Er1
  • Wang, Wenzhe2
  • Fang, Mengdie2
  • Wang, Wei3
  • Xie, Ruifei4
  • Zhou, Hong3
  • Ye, Jian1
  • Xu, Rujun3
  • Ma, Shenglin4
  • 1 Department of Respiratory Medicine, Nanjing Medical University, Affiliated to Hangzhou First People's Hospital, Hangzhou, Zhejiang 310006, P.R. China. , (China)
  • 2 Center for Molecular Medicine, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang 310012, P.R. China. , (China)
  • 3 Department of Pathology, Nanjing Medical University, Affiliated to Hangzhou First People's Hospital, Hangzhou, Zhejiang 310006, P.R. China. , (China)
  • 4 Department of Medical Oncology, Nanjing Medical University, Affiliated to Hangzhou First People's Hospital, Hangzhou, Zhejiang 310006, P.R. China. , (China)
Type
Published Article
Journal
Oncology Letters
Publisher
Spandidos Publications
Publication Date
Jan 01, 2019
Volume
17
Issue
1
Pages
502–507
Identifiers
DOI: 10.3892/ol.2018.9537
PMID: 30655793
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

G protein-coupled receptor, family C, group 5 member A (GPRC5A) is a retinoid-inducible protein, which has been characterized as a tumor-suppressor gene in lung cancer. The present study further examined GPRC5A expression in non-small cell lung cancer (NSCLC) for any association with the clinical features and treatment outcomes of patients with NSCLC. A total of 30 paired NSCLC tumor and adjacent normal tissues were analyzed for the detection of GPRC5A mRNA and protein using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and western blot analysis, respectively. Immunohistochemistry was performed to determine the GPRC5A expression levels in 110 NSCLC and 60 para-tumor tissues. The results confirmed significantly lower expression levels of GPRC5A in NSCLC tumors compared with the corresponding noncancerous tissues (P<0.001). Lost GPRC5A expression was significantly associated with the tumor histological type (P=0.008), poor tumor differentiation (P<0.001) and tumor-node-metastasis (TNM) stage (P<0.001). Kaplan-Meier curve analysis revealed that patients with NSCLC with low GPRC5A expression tumors had a worse prognosis compared with those with high GPRC5A expression tumors (P=0.010). The results of multivariate Cox analysis further suggested that low GPRC5A expression was an independent prognostic factor for patients with NSCLC (P<0.001). The results of this study suggest GPRC5A expression has clinical potential as a prognostic biomarker for patients with NSCLC.

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