Literature DB >> 31250711

Utility of G protein-coupled receptor 35 expression for predicting outcome in colon cancer.

Haytham Ali1,2,3, Manar AbdelMageed1,2,3, Lina Olsson1, Anne Israelsson1, Gudrun Lindmark4, Marie-Louise Hammarström1, Sten Hammarström1, Basel Sitohy2.   

Abstract

The utility of mRNA and protein determinations of G protein-coupled receptor 35, that is, GPR35a (GPR35 V1) and GPR35b (GPR35 V2/3), as indicators of outcome for colon cancer patients after curative surgery was investigated. Expression levels of V1 and V2/3 GPR35, carcinoembryonic antigen and CXCL17 mRNAs were assessed in primary tumours and regional lymph nodes of 121 colon cancer patients (stage I-IV), colon cancer cell lines and control colon epithelial cells using real-time quantitative reverse transcriptase-polymerase chain reaction. Expression of G protein-coupled receptor 35 was investigated by two-colour immunohistochemistry and immunomorphometry. GPR35 V2/3 mRNA, but not V1 mRNA, was expressed in colon cancer cell lines, primary colon tumours and control colon epithelial cells. Haematoxylin and eosin positive (H&E(+)), but not H&E(-), lymph nodes expressed high levels of GPR35 V2/3 mRNA (P<0.0001). GPR35b and carcinoembryonic antigen proteins were simultaneously expressed in many colon cancer tumour cells. Kaplan-Meier and hazard ratio analysis revealed that patients with lymph nodes expressing high levels of GPR35 V2/3 mRNA and, in particular, in the group of patients with lymph nodes also expressing carcinoembryonic antigen mRNA, had a short disease-free survival time, 67 months versus 122 months at 12-year follow-up (difference: 55 months, P = 0.001; hazard ratio: 3.6, P = 0.002). In conclusion, high level expression of G protein-coupled receptor 35 V2/3 mRNA in regional lymph nodes of colon cancer patients is a sign of poor prognosis.

Entities:  

Keywords:  CEA; CXCL17 mRNA; GPR35 V1 mRNA; GPR35 V2/3 mRNA; GPR35b; colon cancer; immunohistochemistry; qRT-PCR

Mesh:

Substances:

Year:  2019        PMID: 31250711     DOI: 10.1177/1010428319858885

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


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