Liu Shuli, Ye Dongxia, Wang Tong, Guo Wenzheng, Song Hongyong, Liao Yueling, Xu Dongliang, Zhu Hanguang, Zhang Zhiyuan, Deng Jiong
Department of Oral and Maxillofacial-Head and Neck Oncology, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Key laboratory of cell differentiation and apoptosis of Chinese Minister of Education, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Cancer Cell Int. 2017 Mar 2;17:34. doi: 10.1186/s12935-017-0406-x. eCollection 2017.
G protein-coupled receptor family C group 5 member A (GPRC5A), a retinoic acid-inducible gene, is a lung tumor suppressor. Previously, we showed that repression of GPRC5A expression was associated with pathologic differentiation grade of oral squamous cell carcinomas (OSCC) and overexpression of GPRC5A gene inhibited the malignant phenotype in OSCC cells, suggesting that GPRC5A also functions as a tumor suppressor in oral cancer. However, the molecular mechanisms underlying GPRC5A deficiency in head and neck squamous cell carcinoma (HNSCC) are still unclear.
In this study, we used Western blot analysis and immunohistochemical (IHC) staining to investigate the expression of GPRC5A in both HNSCC cell lines and clinical samples. GPRC5A stable transfectants and their parental HNSCC cells were characterized for their biological activities in anchorage-independent growth.
IHC analysis showed that, GPRC5A expression was high in normal tissue, but gradually decreased in oral leukoplakia, a precancerous stage, and greatly suppressed in primary cancer. Repression of GPRC5A was correlated with activated STAT3, which associates with aggressive clinicopathological features in HNSCC patients. Moreover, overexpression of GPRC5A suppressed IL-6-induced-STAT3 activation and inhibited anchorage-independent growth in HNSCC cells.
Repressed GPRC5A associates with increased tumor grade and activated STAT3, which may be used as a prognostic marker for tumor progression of HNSCC.
G蛋白偶联受体C家族第5组成员A(GPRC5A)是一种视黄酸诱导基因,是一种肺肿瘤抑制因子。此前,我们发现GPRC5A表达的抑制与口腔鳞状细胞癌(OSCC)的病理分化程度相关,GPRC5A基因的过表达抑制了OSCC细胞的恶性表型,这表明GPRC5A在口腔癌中也起着肿瘤抑制因子的作用。然而,头颈部鳞状细胞癌(HNSCC)中GPRC5A缺乏的分子机制仍不清楚。
在本研究中,我们使用蛋白质免疫印迹分析和免疫组织化学(IHC)染色来研究GPRC5A在HNSCC细胞系和临床样本中的表达。对GPRC5A稳定转染子及其亲本HNSCC细胞进行非锚定依赖性生长的生物学活性鉴定。
免疫组化分析显示,GPRC5A在正常组织中表达较高,但在癌前阶段的口腔白斑中逐渐降低,在原发性癌中受到极大抑制。GPRC5A的抑制与激活的STAT3相关,而STAT3与HNSCC患者侵袭性临床病理特征相关。此外,GPRC5A的过表达抑制了IL-6诱导的STAT3激活,并抑制了HNSCC细胞的非锚定依赖性生长。
GPRC5A的抑制与肿瘤分级增加和STAT3激活相关,这可能作为HNSCC肿瘤进展的预后标志物。