Chordoma is a special malignant tumor that lacks effective therapeutic targets, which can lead to incomplete treatment and metastasis. Inflammation plays an important role in chordoma progression and malignant phenotype. Inflammatory factors such as NF-kappaB and STAT3 are continuously activated in many tumors and contribute to the malignant phenotype of tumors and are potential therapeutic targets. This study suggest TNF-alpha and NF-kappaB signaling pathways were consistently activated in chordomas. Long-term TNF-alpha treatment induces chordoma resistance to EGFR family inhibitors. The underlying mechanism is realized by the key molecules HS3ST3A and HS3ST3B1. These two enzymes are potential targets for chordoma treatment, as well as for combination drugs treatment. It should be emphasized that the above analysis lacks experimental verification.
Analysis of long-term TNF-alpha induced EGFR tyrosine kinase inhibitor resistance in chordoma.
分析脊索瘤中长期 TNF-α 诱导的 EGFR 酪氨酸激酶抑制剂耐药性
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作者:Tang HaoShuai, Zhu QingRun, Fan JinHong, Li XinAo, Yan ZhenYe, Wang Feng, Wang HaiFeng, Wang DaChuan
| 期刊: | RSC Medicinal Chemistry | 影响因子: | 3.600 |
| 时间: | 2025 | 起止号: | 2025 Sep 9 |
| doi: | 10.1039/d5md00258c | 靶点: | EGFR |
| 研究方向: | 信号转导 | ||
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