Aluminum chloride causes 5-fluorouracil resistance in hepatocellular carcinoma HepG2 cells.
Mengling LiZheng-Guo CuiShahbaz Ahmad ZakkiQianwen FengLu SunLoreto B FerilHidekuni InaderaPublished in: Journal of cellular physiology (2019)
Chemoresistance is one of the major obstacles in chemotherapy-based hepatocellular carcinoma (HCC) intervention. Aluminum (Al) is an environmental pollutant that plays a vital role in carcinogenesis, tumorigenesis, and metastasis. However, the effect of Al on chemoresistance remains unknown. 5-Fluorouracil (5-FU) is a widely used antitumor drug. Therefore, we investigated the effects of aluminum chloride (AlCl3 ) on the chemoresistance of HepG2 cells to 5-FU and explored the underlying mechanisms of these effects. The results demonstrated that AlCl3 pretreatment attenuated 5-FU-induced apoptosis through Erk activation and reversed 5-FU-induced cell cycle arrest by downregulating p-Chk2Thr68 levels. In addition, AlCl3 markedly increased the levels of proteins associated with cell migration, such as MMP-2 and MMP-9. Further investigation demonstrated that an Erk inhibitor (U0126) reversed the AlCl3 -induced decrease in apoptosis, enhancement of cell cycle progression, promotion of cell migration, and attenuation of oxidative stress. In summary, AlCl3 induced chemoresistance to 5-FU in HepG2 cells. The present study suggests a potential influence of AlCl3 on 5-FU therapy. These findings may help others to understand and properly address the resistance of HCC to chemotherapeutic agents.
Keyphrases
- cell migration
- oxidative stress
- diabetic rats
- induced apoptosis
- cell cycle arrest
- cell cycle
- signaling pathway
- endoplasmic reticulum stress
- pi k akt
- high glucose
- cell proliferation
- cell death
- randomized controlled trial
- drug induced
- squamous cell carcinoma
- cancer stem cells
- mass spectrometry
- climate change
- heat stress
- high speed