Lemeng Zhang, Jianhua Chen, Lemeng Zhang
Thoracic medicine department, hunan cancer hospital
Objective:Recent studies indicate that autophagy is
adouble-edged sword in tumor genesis and plays an important role in theresistance
of cancer cells to chemotherapy. We hypothesize that autophagy protects against
cisplatin induced apoptotic cell death in A549 human lung cancer cells. Method:Autophagy activity was measured by Western blotting, immunofluoresence
staining, and transmission electron microscopy. Apoptoticcell death was
measured by caspase-3 activity, flowcytometry, and MTT and LDH release.
Cisplatin induced autophagy related gene activation was measured by QPCR and
WB. Result: Cisplatin leads to apoptotic cell death in A549 cells in a
dose- and time- dependent manner; meanwhile, it triggers autophagy response as
demonstrated by increased conversion of LC3BI to LC3BII, increased LC3B punctate
and autophagosomes formation. We further explore the relationship between
cisplatin induced apoptotic cell death and autophagy. Pharmacologic
inhibitionof autophagy by 3-MA and CQ impaired the elimination of damaged
mitochondria, increased caspase-3 activity and thus decreased A549 cell
viability. Furthermore, we found that cisplatin induced autophagy with
alternating significantly thetranscription and expression of Beclin 1, Atg5,
while the up regulation of Atg1/Ulk1, Atg3, Atg7, Atg12, LC3B, and SQSTM1/p62
were not significant. And down regulating Atg5 and Beclin 1 by siRNA, impaired
cisplatin induced autophagic activation, increased accumulation of damaged
mitochondrial in cytoplasm and increased caspase-3activity and thus decreased
A549 cell viability. It demonstrates thatdisruption of autophagy may sensitize
A549 cells to cisplatin induced apoptoticcell death. Conclusion: Suppression
of autophagy, both by pharmacologic interventions and by knockdown autophagy
related genes atg5 and beclin-1, sensitizes A549 tumor cells to cisplatin
induced apoptotic cell death. These findingssuggest a rationale to modulate
autophagy in anti-lung cancer therapy.
Key
Words: autophagy
apoptosis cisplatin
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