- Author:
Tian TANG
1
;
Qing Jie XIA
2
;
Xiaoming QIAO
3
;
Mingrong XI
4
Author Information
- Publication Type:Journal Article
- Keywords: CXCR7; laryngeal cancer; maxillary sinus carcinoma; nasal polyposis
- MeSH: Aged; Biomarkers, Tumor; biosynthesis; genetics; Carcinoma, Squamous Cell; genetics; metabolism; pathology; Disease Progression; Female; Gene Expression Regulation, Neoplastic; Humans; Male; Middle Aged; Otorhinolaryngologic Neoplasms; genetics; metabolism; pathology; RNA, Neoplasm; genetics; Real-Time Polymerase Chain Reaction; Receptors, CXCR; biosynthesis; genetics
- From:Singapore medical journal 2016;57(3):157-160
- CountrySingapore
- Language:English
-
Abstract:
INTRODUCTIONC-X-C chemokine receptor type 7 (CXCR7) has recently been characterised as a novel receptor for the C-X-C motif chemokine 12 (CXCL12)/stromal cell-derived factor 1-alpha. CXCR7 has been thought to play an important role in the pathogenesis of chronic rhinosinusitis, angiogenesis and tumour metastasis. The present study aimed to examine the expression of CXCR7 in tissue samples of laryngeal cancer and maxillary sinus carcinoma to determine its role in the development of otorhinolaryngologic neoplasms.
METHODSSamples of otorhinolaryngologic neoplasms were obtained from 17 patients with either nasal polyps (n = 7), laryngeal cancer (n = 5) or maxillary sinus carcinoma (n = 5), and who underwent surgical resection at West China Hospital of Sichuan University. Total RNA was isolated and CXCR7 mRNA expression was examined and quantified by relative real-time reverse transcription polymerase chain reaction. A one-way analysis of variance was performed using SPSS Statistics version 11.0 (SPSS Inc, Chicago, IL, USA) to compare the CXCR7 mRNA levels among the three groups of patients.
RESULTSAll samples tested positive for CXCR7 mRNA. The quantitative results showed that the CXCR7 mRNA levels were highest in laryngeal cancer and lowest in maxillary sinus carcinoma neoplasms, although there was no significant difference among the three samples.
CONCLUSIONCXCL12 and its receptor CXCR7 may contribute to eosinophilic inflammation in patients with chronic sinusitis and nasal polyps. Our results also suggest that CXCR7 may play a role in the progression, metastasis and angiogenesis of otorhinolaryngologic tumours.