Stem Cell Biology Group, Waghmare Lab, Cancer Research Institute, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai 410210, India.
Department of Head and Neck Oncology, Tata Memorial Hospital, Mumbai 400012, India.
Oncol Rep. 2019 Apr;41(4):2289-2298. doi: 10.3892/or.2019.7003. Epub 2019 Feb 7.
Oral squamous cell carcinoma (OSCC) is a leading cause of mortality in India owing to the high percentage of tobacco chewers, smokers and alcohol consumption. OSCC is highly heterogeneous in nature; therefore poses a challenge in the treatment of the patient. To better understand the heterogeneity of the tumors, an in vitro cell line model is required. However, the efficiency of establishing cell lines from the oral tumors is low. In the present study, three novel cell lines, namely ACOSC3, ACOSC4, and ACOSC16, were isolated and characterized from advanced‑stage treatment‑naive OSCCs originating from the buccal mucosa. The three cell lines exhibited polygonal morphology, which is typical of epithelial cells. Furthermore, immunofluorescence revealed the expression of keratins 8 and 14, thereby confirming the epithelial origin of the cells. DNA content analysis of the three OSCC cell lines revealed aneuploidy. Furthermore, an in vitro orosphere assay revealed the formation of primary orospheres. Notably, the OSCC cell lines were able to give rise to tumors when administered subcutaneously into non‑obese diabetic/severe combined immune deficiency mice. The novelty of the cell lines was also validated by performing short tandem repeat profiling; the STR profiles of the present cell lines did not significantly match with any known established OSCC cell lines present in the DSMZ database, thereby confirming the unique identity of these lines. These cell lines established from tumor samples derived from Indian OSCC patients provide a valuable resource to understand the molecular mechanism involved in tumor resistance and recurrence.
口腔鳞状细胞癌(OSCC)是印度导致死亡率较高的主要原因,这是由于咀嚼烟草、吸烟和饮酒的比例较高。OSCC 在性质上高度异质,因此对患者的治疗构成挑战。为了更好地理解肿瘤的异质性,需要建立体外细胞系模型。然而,从口腔肿瘤中建立细胞系的效率较低。在本研究中,从起源于颊黏膜的晚期初治 OSCC 中分离并鉴定了三个新的细胞系,即 ACOSC3、ACOSC4 和 ACOSC16。这三个细胞系表现出多边形形态,这是上皮细胞的典型特征。此外,免疫荧光显示角蛋白 8 和 14 的表达,从而证实了细胞的上皮起源。对三个 OSCC 细胞系的 DNA 含量分析显示存在非整倍体。此外,体外球体形成试验显示出初级球体的形成。值得注意的是,当将 OSCC 细胞系皮下注射到非肥胖型糖尿病/严重联合免疫缺陷小鼠中时,它们能够形成肿瘤。通过短串联重复序列(STR)分析也验证了细胞系的新颖性;这些细胞系的 STR 谱与 DSMZ 数据库中存在的任何已知的已建立的 OSCC 细胞系没有显著匹配,从而确认了这些细胞系的独特身份。这些从印度 OSCC 患者的肿瘤样本中建立的细胞系为了解肿瘤耐药和复发涉及的分子机制提供了宝贵的资源。