Premium
Overexpression of leucine‐rich repeat‐containing G protein‐coupled receptor 5 in gastric cancer
Author(s) -
Yamanoi Kazuhiro,
Fukuma Mariko,
Uchida Hiroshi,
Kushima Ryoji,
Yamazaki Ken,
Katai Hitoshi,
Kanai Yae,
Sakamoto Michiie
Publication year - 2013
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1111/pin.12013
Subject(s) - malignancy , messenger rna , cancer , lymphovascular invasion , in situ hybridization , receptor , metastasis , pathology , biology , lymphatic system , biomarker , medicine , cancer research , gene , biochemistry
Gastric cancer is one of the most common malignancies worldwide and patients with advanced gastric cancer still have poor clinical outcomes. The overexpression of leucine‐rich repeat‐containing G protein‐coupled receptor 5 ( LGR 5) mRNA in colorectal cancer and its correlation with clinicopathological factors were recently reported by us. In this study, we show LGR 5 mRNA overexpression in human gastric cancer specimens by quantitative RT‐PCR and in situ hybridization and assess a correlation with clinicopathological factors. The mean expression of LGR 5 mRNA in cancerous tissues was five times higher than that in normal tissue ( P = 0.0002). Furthermore, LGR 5 mRNA expression show marked variation among cases and significantly increased in cases where lymphatic invasion was present compared with those where it was absent ( P = 0.0056). Although the mean expression level of LGR 5 was observed to be higher in nodal metastasis and venous invasion positive cases compared to negative cases, a significant difference was not observed. These results suggest that LGR 5 can be a biomarker for malignancy in gastric cancer.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom