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The multidrug resistance can be reversed for the decrease of P-gp and LRP by inhibiting PI3K/Akt/NF-κB signal pathway
Jin Liu1,2, Mingyi Zhu3, Yun Feng4
1Post-Doctoral Station of Combination of Chinese Traditional and Western Medicine, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China.
Aim:
To investigate the relationship between PI3K/Akt/NF-κB cellular signal pathway and the expression of P-gp and LRP in multidrug resistance (MDR) cell of nasopharyngeal carcinoma.
Method:
The PI3K, p-Akt and NF-κB/p65 as the activity of PI3K/Akt/NF-κB were detected by Western blot. The expressions of LRP and P-gp were detected by Western blot and real-time PCR.
Result:
The RIs of CNE/DDP group to DDP, 5-Fu, VCR, ADR and PTX were 35.04, 18.14, 24.13, 12.00 and 10.18, respectively. The RIs of LY-294002 group were 11.77, 5.83, 3.07, 3.86 and 3.34, and PDTC group were 11.08, 6.55, 7.66, 2.18 and 4.05. The expressions of PI3K, p-Akt and NF-κBp65, LRP and P-gp were increased and mRNA of LRP and P-gp were up-regulated in CNE/DDP. The expression of p-Akt in LY-294002 group was down-regulated. The expression of NF-κB p65 in PDTC group was decreased. The mRNA of LRP and P-gp in LY-294002 group and PDTC group were decreased.
Conclusion:
MDR of nasopharyngeal carcinoma cell can be regulated by activating PI3K/Akt/NF-κB signal pathway and then increase the expression of P-gp and LRP. The MDR of nasopharyngeal carcinoma cell can be reversed by inhibiting PI3K/Akt/NF-κB signal pathway.
Insights
The PI3K/Akt/NF-κB pathway activation increases P-gp and LRP expression, contributing to multidrug resistance in nasopharyngeal carcinoma cells. Inhibiting this pathway can reverse multidrug resistance, offering a potential therapeutic strategy.
Area of Science:
- Oncology
- Molecular Biology
- Cellular Signaling
Background:
- Nasopharyngeal carcinoma (NPC) often develops multidrug resistance (MDR).
- The PI3K/Akt/NF-κB signaling pathway is implicated in various cellular processes, including drug resistance.
- P-glycoprotein (P-gp) and Lung Resistance-Related Protein (LRP) are key efflux pumps associated with MDR.
Purpose of the Study:
- To elucidate the role of the PI3K/Akt/NF-κB signaling pathway in the expression of P-gp and LRP in NPC MDR cells.
- To investigate whether modulating this pathway affects NPC drug resistance.
Main Methods:
- Western blot was used to detect the activity of the PI3K/Akt/NF-κB pathway (PI3K, p-Akt, NF-κB/p65).
- Real-time PCR and Western blot were employed to measure the expression levels of P-gp and LRP.
- Specific inhibitors (LY-294002 for PI3K and PDTC for NF-κB) were used to modulate pathway activity.
Main Results:
- NPC cells (CNE/DDP) exhibited increased expression of PI3K, p-Akt, NF-κB/p65, P-gp, and LRP, along with elevated mRNA levels of P-gp and LRP.
- Inhibition of the PI3K/Akt/NF-κB pathway using LY-294002 and PDTC led to decreased expression of p-Akt, NF-κB p65, and consequently, reduced mRNA levels of P-gp and LRP.
- Drug resistance indices (RIs) were significantly reduced in inhibitor-treated groups compared to the CNE/DDP group.
Conclusions:
- Activation of the PI3K/Akt/NF-κB pathway upregulates P-gp and LRP expression, contributing to multidrug resistance in nasopharyngeal carcinoma.
- Inhibition of the PI3K/Akt/NF-κB signaling pathway can reverse multidrug resistance in nasopharyngeal carcinoma cells, suggesting its potential as a therapeutic target.
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