Stemness state regulators SALL4 and SOX2 are involved in progression and invasiveness of esophageal squamous cell carcinoma

• Published in: Medical oncology (Northwood, London, England) London, England), 2014-04, Vol.31 (4), p.922-922, Article 922
• Main Authors: Forghanifard, Mohammad Mahdi, Ardalan Khales, Sima, Javdani-Mallak, Afsaneh, Rad, Abolfazl, Farshchian, Moein, Abbaszadegan, Mohammad Reza
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Carcinoma, Squamous Cell - metabolism; Disease Progression; Esophageal Neoplasms - metabolism; Esophageal Squamous Cell Carcinoma; Esophagus - metabolism; Female; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Hematology; Humans; Internal Medicine; Male; Medicine; Medicine & Public Health; Middle Aged; Neoplasm Invasiveness; Neoplasm Metastasis; Neoplastic Stem Cells - metabolism; Oncology; Original Paper; Pathology; Real-Time Polymerase Chain Reaction; SOXB1 Transcription Factors - genetics; SOXB1 Transcription Factors - physiology; Transcription Factors - genetics; Transcription Factors - physiology
• ISSN: 1357-0560; 1559-131X
• DOI: 10.1007/s12032-014-0922-7

Cancer stem cells, as a subgroup of tumor cells, resemble critical properties of embryonic stem cells (ESCs) such as self-renewal and maintenance of stemness state. SALL4 and SOX2 are two main transcription factors involving in maintenance of pluripotency, self-renewal and cell fate decision in ESCs. In this study, we aimed to elucidate the expression levels of these important transcription factors in esophageal squamous cell carcinoma (ESCC) and to reveal their probable roles in maintenance and progression of the disease. The expression level of SALL4 and SOX2 was analyzed in fresh tumoral tissues in comparison with distant tumor-free tissues of 50 ESCC patients by relative comparative real-time PCR. SALL4 and SOX2 were overexpressed in 64 and 32 % of tumor samples, respectively, in significant correlation with each other ( p  = 0.028). There was a significantly inverse correlation between low level of SALL4 expression and metastasis of tumor cells into the lymph nodes ( p  = 0.035). Furthermore, co-overexpression of the genes was significantly correlated with the depth of tumor invasion ( p  = 0.045) and metastasis to the lymph nodes ( p  = 0.049). SALL4 and SOX2 are co-overexpressed in ESCC and have a significant correlation with invasion and metastasis of the disease. To the best of our knowledge, this is the first report of SALL4 clinical relevance in ESCC to date. The clinical consequences of SALL4 – SOX2 association suggest a possible functional interaction between these factors in regulation of ESCC maintenance and aggressiveness and introduce these regulators of stemness state as potentially interesting therapeutic targets to bring new opportunities for onco-therapeutic modalities.