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Published on: January 5, 2017
Inhibition Mechanism of PinX1 Gene on Cancer Stem Cells of Nasopharyngeal Carcinoma
Hua Xiang1, Linghui Liu2, Yuzhu Yuan3
1Department of Otolaryngology Head and Neck Surgery, Central Hospital of Enshi Tujia and Miao Autonomous Prefecture (Enshi Clinical College, Wuhan University), Enshi, 445000, Hubei Province, China. xueque143812804@163.com.
Abstract:
The recurrence and long-term metastasis of these tumors are important causes of treatment failure and death. On the other hand, PinX1 is a nucleolar protein found in recent years that can interact with telomere/telomerase simultaneously, and it is highly conserved in human and yeast. Some studies have shown that the PinX1 gene can inhibit the tumor stem cells of NPC. Therefore, the mechanism of inhibition of the PinX1 gene on the tumor stem cells of NPC has been studied in this paper. In this paper, CNE2 cells of NPC were used as experimental materials, CD133 as a marker, PinX1 overexpression plasmids and their corresponding empty plasmids were respectively transfected in CD133+ cells, PinX1 siRNA and their corresponding NC siRNA were respectively transfected in CD133- cells for control experiments. In this study, we found that the telomerase activity of the CD133 - + NC group was 1.001 ± 0.086, the CD133 - + pinx1sirna group was 0.974 ± 0.046, CD133+ + vector group was 0.928 ± 0.102, CD133+ + over PinX1 group was 0.703 ± 0.086. Therefore, the PinX1 gene can inhibit NPC stem cells by inhibiting telomerase activity.
Insights
PinX1 inhibits nasopharyngeal carcinoma (NPC) stem cells by reducing telomerase activity. This finding offers a new therapeutic target for treating NPC, a cancer known for recurrence and metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Nasopharyngeal carcinoma (NPC) recurrence and metastasis are major causes of treatment failure and mortality.
- PinX1, a nucleolar protein, interacts with telomere/telomerase and is conserved across species.
- Previous research suggests PinX1 inhibits NPC tumor stem cells.
Purpose of the Study:
- To investigate the mechanism by which the PinX1 gene inhibits NPC tumor stem cells.
Main Methods:
- Utilized CNE2 cells from NPC as experimental material.
- Employed CD133 as a marker for tumor stem cells.
- Transfected CD133+ cells with PinX1 overexpression plasmids and CD133- cells with PinX1 siRNA for functional studies.
Main Results:
- Telomerase activity was significantly reduced in CD133+ cells overexpressing PinX1 (0.703 ± 0.086) compared to vector controls (0.928 ± 0.102).
- PinX1 siRNA in CD133- cells showed comparable telomerase activity to controls (0.974 ± 0.046 vs. 1.001 ± 0.086).
Conclusions:
- The PinX1 gene inhibits NPC stem cells.
- This inhibition is achieved by suppressing telomerase activity.
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