Ginsenoside Rh2 Induces HeLa Apoptosis through Upregulating Endoplasmic Reticulum Stress-Related and Downstream Apoptotic Gene Expression

• Published in: Molecules (Basel, Switzerland) Vol. 27; no. 22; p. 7865
• Main Authors: Liu, Ying, Wang, Xinran, Qiao, Juhui, Wang, Jiawen, Jiang, Leilei, Wang, Chenxi, Yu, Shiting, Zhang, Peiguang, Zhao, Daqing, Fan, Meiling, Liu, Meichen
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01-11-2022; MDPI
• Subjects: Annexin V; Apoptosis; Apoptosis Regulatory Proteins; Biological activity; Cancer; Cancer therapies; Care and treatment; Caspase-3; Cell growth; Cell viability; Cervical cancer; Cervix; Cholecystokinin; Drug dosages; Encyclopedias; Endoplasmic reticulum; Endoplasmic Reticulum Stress; Female; Gene Expression; Genes; Genomes; ginsenoside Rh2; HeLa Cells; Humans; Malignancy; Molecular docking; Molecular Docking Simulation; Proteins; RNA; RNA-seq; Signal transduction; Transcriptomes; Uterine Cervical Neoplasms - drug therapy; Uterine Cervical Neoplasms - genetics; China; apoptosis; molecular docking; RNA-seq; ginsenoside Rh2; cervical cancer; endoplasmic reticulum stress
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules27227865

Cervical cancer is a common gynecological malignancy afflicting women all over the world. Ginsenoside Rh2 (GRh2), especially 20(S)-GRh2, is a biologically active component in the natural plant ginseng, which can exhibit anticancer effects. Here, we aimed to investigate the effect of 20(S)-GRh2 on cervical cancer and elucidate the underlying mechanism through RNA-seq. In this study, the CCK-8 assay showed that 20(S)-GRh2 inhibited HeLa cell viability in a time- and dose-dependent manner. Caspase 3 activity and Annexin V staining results showed that 20(S)-GRh2 induced apoptosis of HeLa cells. Gene function enrichment analysis revealed that the biological process gene ontology (GO) terms were associated with the apoptotic signaling pathway. Biological process GO terms' similarity network indicated that apoptosis might be from endoplasmic reticulum stress (ERs). Kyoto Encyclopedia of Genes and Genomes enrichment analysis revealed that 20(S)-GRh2 primarily modulates apoptosis pathway genes. Combined protein-protein interaction network, hub gene screening, and qPCR validation data showed that ERs-related genes (ATF4 and DDIT3) and the downstream apoptotic genes (JUN, FOS, BBC3, and PMAIP1) were potential novel targets of 20(S)-GRh2-inducing cervical cancer cell apoptosis. Differential transcript usage analysis indicated that DDIT3 is also a differential transcript and its usage of the isoform (ENST00000552740.5) was reduced by 20(S)-GRh2. Molecular docking suggested that 20(S)-GRh2 binds to the targets (ATF4, DDIT3, JUN, FOS, BBC3, and PMAIP1) with high affinity. In conclusion, our findings indicated that 20(S)-GRh2 might promote ERs-related apoptosis of cervical cancer cells by regulating the DDIT3-based targets' signal pathway. The role of 20(S)-GRh2 at the transcriptome level provides novel targets and evidence for the treatment of cervical cancer.