Bibliographic Details
| Title: |
PUM1-TRAF3 fusion protein activates non-canonical NF-κB signaling via rescued NIK in biliary tract cancer. |
| Authors: |
Jung, Dawoon E., Seo, Mi-Kyoung, Jo, Jung Hyun, Kim, Kahee, Kim, Chanyang, Kang, Hyundeok, Park, Soo Been, Lee, Hee Seung, Kim, Sangwoo, Song, Si Young |
| Source: |
NPJ Precision Oncology; 8/1/2024, Vol. 8 Issue 1, p1-14, 14p |
| Subject Terms: |
BILIARY tract cancer, GENE expression, GENE fusion, FLUORESCENCE in situ hybridization, CHROMOSOMAL translocation |
| Abstract: |
Discovery and verification of diagnostic or therapeutic biomarkers for biliary tract cancer (BTC) is challenging owing to the low prevalence of the disease. Here, we identified and investigated the clinical impact of a fusion gene, Pumilio1-tumor necrosis factor receptor-associated factor 3 (PUM1-TRAF3), caused by 1;14 chromosomal translocation in BTC. PUM1-TRAF3 was initially identified in the RNA-sequencing of five BTC surgical tissues and confirmed by fluorescence in situ hybridization. Expression of the fusion gene was validated in an expanded cohort (5/55, 9.1%). Establishment and molecular assessment of PUM1-TRAF3 expressing BTC cells revealed that PUM1-TRAF3 activates non-canonical NF-κB signaling via NF-κB-inducing kinase (NIK). Abnormal TRAF3 activity, driven by competitive binding of PUM1-TRAF3 and TRAF3 to NIK, led to NIK rescue followed by P52/RelB nuclear translocation, all of which were reverted by an NIK inhibitor. The elevated expression of NIK and activated NF-κB signaling was observed in the PUM1-TRAF3-expressing regions of patient tissues. Expression of the PUM1-TRAF3 fusion was significantly correlated with strong NIK expression, which is associated with a poorer prognosis for patients with BTC. Overall, our study identifies a new fusion gene, PUM1-TRAF3, that activates NIK and non-canonical NF-κB signaling, which may be beneficial for developing precise treatment strategies for BTC. [ABSTRACT FROM AUTHOR] |
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| Database: |
Complementary Index |
