4.4 Article

Upregulation of BNIP3 mediated by ERK/HIF-1α pathway induces autophagy and contributes to anoikis resistance of hepatocellular carcinoma cells

Journal

FUTURE ONCOLOGY
Volume 10, Issue 8, Pages 1387-1398

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/FON.14.70

Keywords

anoikis resistance; autophagy; BNIP3; hepatocellular carcinoma; mTOR/S6K1

Categories

Funding

  1. National Nature Science Foundation of China [81172352, 30700357]
  2. Science and Technology Development Project of Shandong Province [2011GGE27020]
  3. Outstanding Youth Scientific Fund of Shandong Province [BS2013YY037]
  4. Scientific Research Project in Jinan City [201112007, 20080211]

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Aim: Acquisition of anoikis resistance is the hallmark of cancer and has been shown to be involved in metastasis of melignant cells. Our previous work showed that anoikis resistance is associated with the metastasis of hepatocellular carcinoma (HCC) cells. The aim of this study is to elucidate the mechanisms of this course. Materials & methods: Expression of BNIP3 and HIF-1 alpha at the mRNA and protein level in HCC cells were detected by realtime PCR and western blot, respectively. Autophagy activation and signaling transduction pathway were detected by western blot. Cell viabilities were detected by CCK8 assay and trypan blue exclusion assay. Results: Upregulation of BNIP3 promoted the activation of autophagy, one type of cell survival strategy in response to external stress, by suppressing mTOR/S6K1 signaling system. The upregulation of BNIP3 was mediated by ERK/HIF-1 alpha pathway, which further contributed to anoikis resistance of HCC cells through the mTORC1 signaling pathway. Conclusion: Upregulation of BNIP3 contributs to anoikis resistance of HCC cells, and BNIP3 may serve as a novel therapeutic target for manipulation of cancer metastasis.

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