Exosomal long noncoding RNA lnc-GNAQ-6:1 may serve as a diagnostic marker for gastric cancer

• Published in: Clinica chimica acta Vol. 501; pp. 252 - 257
• Main Authors: Li, Shibao, Zhang, Miaomiao, Zhang, Haoliang, Hu, Kan, Cai, Chenchen, Wang, Jiwei, Shi, Lubin, Ma, Ping, Xu, Yinhai, Zheng, Peiming
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-02-2020
• Subjects: Exosomes; Gastric cancer; Inc-GNAQ-6:1; Long non coding RNA; Long non coding RNA; Exosomes; Inc-GNAQ-6:1; Gastric cancer
• ISSN: 0009-8981; 1873-3492
• DOI: 10.1016/j.cca.2019.10.047

•The expression of lnc-GNAQ-6:1 was significantly down-regulated in serum of patients with gastric cancer.•Exosomal long noncoding RNA lnc-GNAQ-6:1 may be a new tumor marker for gastric cancer diagnosis.•The higher purity exosomes can be isolated from the sera via this commercial exosome extraction kit.
Gastric cancer (GC) is one of the most aggressive cancers, with limited early diagnostic measures. Tumor-originated exosomal molecules are regarded as suitable candidates for non-invasive diagnosis. This study aimed to investigate the capacity of exosomal long noncoding RNA lnc-GNAQ-6:1 as a biomarker for early diagnosis of GC.
In this study, we collected sera from 43 patients with gastric cancer and 27 healthy subjects, then exosomes were isolated using commercial kits. Particle size analysis, Western bloting and protein-based exosomes quantification were conducted to identify the isolated exosomes and to evaluate its yield and purity. Expression levels of exosomal lnc-GNAQ-6:1 were detected by quantitative reverse transcription PCR (qRT-PCR). The serum concentrations of traditional biomarker (CA72-4, CEA, and CA19-9) were measured via a chemiluminescent detection system.The receiver operating characteristic curve (ROC) and area under curve (AUC) were used to estimate the diagnostic capacity. Furthermore, we analyzed the potential relationship between serum exosomal lnc-GNAQ-6:1 expression and clinicopathological parameters of gastric cancer.
The exosomes extracted in this study exhibited the typical exosome characteristics and purity. Patients with gastric cancer had the higher exosome yield than healthy volunteer. The results of qRT-PCR showed that compared with the healthy control, the expression of lnc-GNAQ-6:1 was significantly lower in the gastric cancer group. The area under the ROC curve is 0.732, which was higher than the diagnostic accuracy of CEA, CA 19–9 and CA72–4. However, the expression level of lnc-GNAQ-6:1 was not correlated with gender, age, tumor metastasis, serum carcinoembryonic antigen (CEA), carbohydrate antigen 19–9 (CA19-9), and carbohydrate antigen 72–4(CA72-4).
Our data demonstrated that serum exosomal lnc-GNAQ-6:1 is lowly expressed in patient with gastric cancer and might be evaluated in larger studies as a new diagnostic marker for gastric cancer.