Caspa Gokulan Ravindran, Devaraj Halagowder
Unit of Biochemistry, Department of Zoology, Guindy Campus, University of Madras, Chennai 600085, Tamil Nadu, India.
Cancers (Basel). 2021 Nov 23;13(23):5895. doi: 10.3390/cancers13235895.
The activation of the SDF-1/CXCR-4 pathway is crucial for the invasion and metastasis of oral cancer cells. The CXCR-4 positive cells possess stem cell characteristics and express the cancer stem cell marker, CD133, in tumors of colon and pancreas. Despite several studies, the co-expression of CXCR-4 and CD133 and its significance is still largely unknown in oral cancer. Therefore, we aimed to investigate the impact of CXCR-4 and CD133 double positivity in the prognosis of oral cancer. The significance of PKC-δ, one of the key signaling molecules that regulates CXCR-4, was also analyzed. Immunohistochemistry and double immunofluorescence was used to investigate the co-localization of CXCR-4, PKC-δ and CD133 in the human tissues and cell lines of oral squamous cell carcinoma. The expression of CXCR-4, PKC-δ and CD133 were found to be higher in poorly differentiated and lymph node metastasis-positive cases. Interestingly, CXCR-4 positive cells showed positive staining for PKC-δ and CD133 in oral cancer tissue and cell lines. Moreover, CXCR-4+/CD133+ and CXCR-4+/PKC-δ+ double positive cases have the worst survival. We discovered, for the first time, that patients with expression of both CXCR-4 and CD133 have a lower survival rate, and CXCR-4+/CD133+, as well as CXCR-4+/PKC-δ+ double positivity, can be utilized to predict poor prognosis. CXCR-4, PKC-δ and CD133 might regulate aggressiveness and invasion of oral cancer cells.
SDF-1/CXCR-4信号通路的激活对口腔癌细胞的侵袭和转移至关重要。CXCR-4阳性细胞具有干细胞特征,并在结肠癌和胰腺癌肿瘤中表达癌症干细胞标志物CD133。尽管已有多项研究,但CXCR-4和CD133的共表达及其意义在口腔癌中仍 largely未知。因此,我们旨在研究CXCR-4和CD133双阳性对口腔癌预后的影响。还分析了调节CXCR-4的关键信号分子之一PKC-δ的意义。采用免疫组织化学和双重免疫荧光法研究CXCR-4、PKC-δ和CD133在口腔鳞状细胞癌人体组织和细胞系中的共定位。发现CXCR-4、PKC-δ和CD133在低分化和淋巴结转移阳性病例中的表达较高。有趣的是,在口腔癌组织和细胞系中,CXCR-4阳性细胞对PKC-δ和CD133呈阳性染色。此外,CXCR-4+/CD133+和CXCR-4+/PKC-δ+双阳性病例的生存率最差。我们首次发现,同时表达CXCR-4和CD133的患者生存率较低,CXCR-4+/CD133+以及CXCR-4+/PKC-δ+双阳性可用于预测预后不良。CXCR-4、PKC-δ和CD133可能调节口腔癌细胞的侵袭性和侵袭能力。 (注:原文中“largely”未准确翻译,推测可能是“很大程度上”之类意思,但根据要求未调整表述)