PNU-74654 Suppresses TNFR1/IKB Alpha/p65 Signaling and Induces Cell Death in Testicular Cancer
- Curr Issues Mol Biol. 2022 Jan 4;44(1):222-232. doi: 10.3390/cimb44010016.
- 1. Institute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
- 2. School of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
- 3. Department of Urology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.
- 4. Department of Obstetrics and Gynecology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.
- 5. Division of Infertility Clinic, Lee Women's Hospital, Taichung 40201, Taiwan.
Testicular Cancer (TC) is a rare malignancy worldwide and is the most common malignancy in males aged 15-44 years. The Wnt/β-catenin signaling pathway mediates numerous essential cellular functions and has potentially important effects on tumorigenesis and Cancer progression. The search for drugs to inhibit this pathway has identified a small molecule, PNU-74654, as an inhibitor of the β-catenin/TCF4 interaction. We evaluated the therapeutic role of PNU-74654 in two TC cell lines, NCCIT and NTERA2, by measuring cell viability, cell cycle transition and cell death. Potential pathways were evaluated by protein arrays and Western blots. PNU-74654 decreased cell viability and induced Apoptosis of TC cells, with significant increases in the sub G1, Hoechst-stained, Annexin V-PI-positive rates. PNU-74654 treatment of both TC cell lines inhibited the TNFR1/IKB alpha/p65 pathway and the execution phase of Apoptosis. Our findings demonstrate that PNU-74654 can induce Apoptosis in TC cells through mechanisms involving the execution phase of Apoptosis and inhibition of TNFR1/IKB alpha/p65 signaling. Therefore, small molecules such as PNU-74654 may identify potential new treatment strategies for TC.