1. Academic Validation
  2. Bmi1 Severs as a Potential Tumor-Initiating Cell Marker and Therapeutic Target in Esophageal Squamous Cell Carcinoma

Bmi1 Severs as a Potential Tumor-Initiating Cell Marker and Therapeutic Target in Esophageal Squamous Cell Carcinoma

  • Stem Cells Int. 2020 Aug 20;2020:8877577. doi: 10.1155/2020/8877577.
Xiaochen Wang 1 Kang Li 1 Maosheng Cheng 1 Ganping Wang 1 Hui Han 1 Fangfang Chen 1 Wenjing Liao 1 Zhi Chen 1 Jianwen Chen 1 Yong Bao 2 Liang Peng 3 Demeng Chen 1
Affiliations

Affiliations

  • 1 Center for Translational Medicine, Institute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510030, China.
  • 2 Department of Radiation Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510030, China.
  • 3 Oncology Department, Chinese PLA General Hospital, Beijing 100000, China.
Abstract

Esophageal squamous cell carcinoma (ESCC) is a frequent malignant tumor with low 5-year overall survival. Targeting ESCC tumor-initiating cells (TICs) may provide a new research avenue to achieve better therapeutic effects of ESCC. However, the identity and characteristics of ESCC TICs remain poorly understood. Through genetic lineage tracing approach, we found that a group of Moloney murine leukemia virus insertion site 1- (Bmi1-) expressing cell populations present in the invasive front of the esophageal epithelium, providing a continuous flow of tumor cells for ESCC. Subsequently, we found that ablation of Bmi1+ cells from mice with ESCC led to inhibition of tumor growth. In addition, our results demonstrated that PTC-209, an inhibitor of Bmi1, was able to inhibit ESCC progression when combined with cisplatin. In summary, our data suggest that Bmi1+ cells serve as TICs in ESCC.

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