A CD90+ Tumor-Initiating Cell Population with an Aggressive Signature and Metastatic Capacity in Esophageal Cancer

Kwan Ho Tang(Sun Yat-sen University), Yong Dai(Sun Yat-sen University), Man Tong(Sun Yat-sen University), Yuen Piu Chan(Sun Yat-sen University), Pak Shing Kwan(Sun Yat-sen University), Li Fu(Sun Yat-sen University), Yan Qin(Sun Yat-sen University), Sai Wah Tsao(Sun Yat-sen University), Hong Lok Lung(Sun Yat-sen University), Maria Li Lung(Sun Yat-sen University), Daniel King Hung Tong(Sun Yat-sen University), Simon Law(Sun Yat-sen University), Kwok Wah Chan(Sun Yat-sen University), Stephanie Ma(Sun Yat-sen University), Xin‐Yuan Guan(Sun Yat-sen University)
Cancer Research
February 4, 2013
Cited by 148

Abstract

Tumor-initiating cells (TIC), also known as cancer stem cells, are regarded widely as a specific subpopulation of cells needed for cancer initiation and progression. TICs have yet to be identified in esophageal tumors that have an increasing incidence in developed countries. Here, we report a CD90(+) cell population found in esophageal squamous cell carcinoma (ESCC), which is endowed with stem cell-like properties and high tumorigenic and metastatic potential. mRNA profiling of these cells suggested pathways through which they drive tumor growth and metastasis, with deregulation of an Ets-1/MMP signaling pathway and epithelial-mesenchymal transition figuring prominently. These cells possessed higher self-renewal activity and were sufficient for tumor growth, differentiation, metastasis, and chemotherapeutic resistance. CD90(+) TICs were isolated and characterized from ESCC clinical specimens as well as ESCC cell lines. In freshly resected clinical specimens, they represented a rare cell population, the levels of which correlated with strong family histories and lymph node metastasis. Our results prompt further study of this CD90(+) population of esophageal TICs as potential therapeutic targets.


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