1. Academic Validation
  2. Crebanine Induces Cell Death and Alters the Mitotic Process in Renal Cell Carcinoma In Vitro

Crebanine Induces Cell Death and Alters the Mitotic Process in Renal Cell Carcinoma In Vitro

  • Int J Mol Sci. 2025 Jul 18;26(14):6896. doi: 10.3390/ijms26146896.
Hung-Jen Shih 1 2 3 Hsuan-Chih Hsu 4 Chien-Te Liu 4 Ya-Chuan Chang 4 5 Chia-Ying Yu 4 5 Wen-Wei Sung 4 5 6
Affiliations

Affiliations

  • 1 Division of Urology, Department of Surgery, Changhua Christian Hospital, Changhua 500, Taiwan.
  • 2 Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung 402, Taiwan.
  • 3 Department of Urology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
  • 4 School of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
  • 5 Department of Urology, Chung Shan Medical University Hospital, Taichung 402, Taiwan.
  • 6 Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
Abstract

Advanced renal cell carcinoma (RCC) has a poor prognosis; this drives the exploration of alternative systemic therapies to identify more effective treatment options. Recent research has revealed that crebanine, an alkaloid derivative of the Stephania genus, induces apoptotic effects in various cancers; however, a thorough investigation of the role of crebanine in RCC has not been conducted thus far. For this study, we evaluated tumor cell viability, clonogenicity, cell-cycle distributions, morphological changes, and cell mortality with the aim of exploring the antitumor effects of crebanine in RCC. Furthermore, we compared gene and protein expressions using RNA Sequencing analysis and Western blotting. The findings indicated that crebanine significantly inhibited RCC colonies and caused G1-phase cell-cycle arrest with sub-G1-phase accumulation, thus leading to suppressed cell proliferation and cell death. In addition, Hoechst 33342 staining was used to observe apoptotic cells, which revealed chromatin condensation and a reduction in the nuclear volume associated with Apoptosis. Further, gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis indicated that differentially expressed genes are involved in the initiation of DNA replication, centrosome duplication, chromosome congression, and mitotic processes in the cell cycle along with signaling pathways, such as I-kappaB kinase/NF-kappaB signaling, Hippo signaling, and intrinsic apoptotic pathways. Consistent with GO and KEGG analyses, increased levels of cleaved Caspase-3, cleaved caspase-7, and cleaved PARP, and decreased levels of cIAP1, BCL2, Survivin, and claspin were observed. Finally, the expressions of G1/S phase transition cyclin D1, cyclin E/CDK2, and cyclin A2/CDK2 complexes were downregulated. Overall, these findings supported the potential of crebanine as an Adjuvant therapy in RCC.

Keywords

Stephania venosa; aporphine alkaloid; kidney cancer; natural product; systemic treatment.

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