1. Inhibition of Phosphatidylinositol 3-kinase (PI3K) Signaling Synergistically Potentiates Antitumor Efficacy of Paclitaxel and Overcomes Paclitaxel-Mediated Resistance in Cervical Cancer
- Author
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Hye Won Lee, Min Wha Baik, Oyoung Kim, Youn Jin Choi, Soo Young Hur, Jung Yoon Ho, and Jing Jing Liu
- Subjects
Cyclin E ,Paclitaxel ,cervical cancer ,Class I Phosphatidylinositol 3-Kinases ,Uterine Cervical Neoplasms ,Antineoplastic Agents ,Apoptosis ,PI3K inhibitor ,Catalysis ,Article ,combination therapy ,Inorganic Chemistry ,HeLa ,lcsh:Chemistry ,chemistry.chemical_compound ,Cell Line, Tumor ,Humans ,LY294002 ,Physical and Theoretical Chemistry ,Enzyme Inhibitors ,Cyclin B1 ,Molecular Biology ,lcsh:QH301-705.5 ,Spectroscopy ,Cyclin-dependent kinase 1 ,biology ,Organic Chemistry ,Cell Cycle ,Genetic Variation ,Drug Synergism ,General Medicine ,Cell cycle ,biology.organism_classification ,invasion ,Computer Science Applications ,paclitaxel resistance ,chemistry ,lcsh:Biology (General) ,lcsh:QD1-999 ,Drug Resistance, Neoplasm ,Cancer research ,Female ,Phosphatidylinositol 3-Kinase ,Cyclin A1 ,Proto-Oncogene Proteins c-akt ,DNA Damage ,Signal Transduction - Abstract
Acquired paclitaxel (PTX) resistance limits its effectiveness and results in advanced cancer progression. This review investigated whether the inhibition of phosphatidylinositol 3-kinase (PI3K) signaling overcomes paclitaxel resistance in cervical cancer. It was established paclitaxel-resistant cell lines (PTX-R ME180/PTX-R HeLa) and determined the combination index for paclitaxel and PI3K inhibitors (BYL-719/ LY294002) by tetrazolium dye assay. Flow cytometry was used to detect the cell cycle and apoptosis. Migration and invasion were explored by wound healing and transwell assays. Genes related to multiple pathways were assessed by a western blot. It was found that the PI3K pathway was significantly activated in paclitaxel-resistant HeLa and ME180 cells compared to parental cells. PTX + PI3K inhibitor combined therapy showed a synergistic effect by strengthening paclitaxel-induced S and G2M arrest in PTX-R cell sublines by the inactivation of cyclin A1, cyclin B1, cyclin E, and Cdc2 expression. Moreover, combination therapy significantly enhanced drug sensitivity and apoptosis through the activation of Bax, and cleavage of poly-(ADP-ribose) polymerase compared with paclitaxel alone. In addition, PI3K inhibition also suppressed tumor migration and invasion by targeting &beta, catenin and matrix metalloproteinase-2/9. The authors suggest that the combination of a PI3K inhibitor with paclitaxel may enhance antitumor activity through a cascade of PI3K signaling events.
- Published
- 2019