Javascript must be enabled to continue!
Abstract 1610: Inhibiting HuR, a RNA-binding protein, for inhibition of pancreatic cancer EMT and CSCs
View through CrossRef
Abstract
Purpose
Epithelial- mesenchymal transition (EMT) contributes importantly to cancer cell metastasis, and formation of cancer stem cells (CSCs). An RNA-binding protein, HuR, plays an important role in many solid tumors for promoting cell proliferation, metastasis, anti-apoptosis and drug resistance. However, the role of HuR in cancer cell EMT and CSC has not been elucidated. Here we aim to investigate the role of HuR in pancreatic cancer EMT and CSC, and developing a new HuR inhibitor ST-3 as an inhibitor for pancreatic cancer EMT and CSCs.
Methods
Fluorescence Polarization assay and surface plasmon resonance assay was utilized for St-3, HuR and target mRNA binding. Scratching assay and matrigel invasion assay were used for cell migration and invasion, whereas MTT assay for viability. Tumor spheroid formation assay was used as an indication of CSCs. Western blot and RT-qPCR was used for protein and mRNA expression.
Results
Knockdown of HuR with siRNA inhibited migration of pancreatic cancer cells MIAPaCa-2, and suppressed the expression of Vimentin, Snail, and increased E-cadherin expression, showing inhibition in EMT. The suppression of Snail is due to accelerated mRNA decay. Overexpression of HuR protected mRNA of Snail from degradation, suggesting that Snail is a direct target of HuR. Knockdown of HuR also decreased pancreatic cancer spheroids formation.
St-3 inhibited the proliferation of pancreatic cancer cell lines more potently in HuR-high cells MIAPaCa-2 (IC50 ∼2 μM), than in HuR-low cells BxPc-3 and PANC-1 (IC50 6-20 μM). St-3 directly bound to HuR, and inhibited binding of HuR with its target mRNAs. St-3 treatment mimicked the HuR knockdown effects in inhibiting cell migration, EMT, and spheroids formation.
Conclusion
HuR is an important regulator in pancreatic cancer EMT and CSCs. ST-3 as a novel HuR inhibitor inhibited pancreatic cancer EMT and CSCs. Further investigation is under way.
Citation Format: Ruochen Dong, Kishore Polireddy, Ying Zhang, Qi Chen. Inhibiting HuR, a RNA-binding protein, for inhibition of pancreatic cancer EMT and CSCs. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 1610.
American Association for Cancer Research (AACR)
Title: Abstract 1610: Inhibiting HuR, a RNA-binding protein, for inhibition of pancreatic cancer EMT and CSCs
Description:
Abstract
Purpose
Epithelial- mesenchymal transition (EMT) contributes importantly to cancer cell metastasis, and formation of cancer stem cells (CSCs).
An RNA-binding protein, HuR, plays an important role in many solid tumors for promoting cell proliferation, metastasis, anti-apoptosis and drug resistance.
However, the role of HuR in cancer cell EMT and CSC has not been elucidated.
Here we aim to investigate the role of HuR in pancreatic cancer EMT and CSC, and developing a new HuR inhibitor ST-3 as an inhibitor for pancreatic cancer EMT and CSCs.
Methods
Fluorescence Polarization assay and surface plasmon resonance assay was utilized for St-3, HuR and target mRNA binding.
Scratching assay and matrigel invasion assay were used for cell migration and invasion, whereas MTT assay for viability.
Tumor spheroid formation assay was used as an indication of CSCs.
Western blot and RT-qPCR was used for protein and mRNA expression.
Results
Knockdown of HuR with siRNA inhibited migration of pancreatic cancer cells MIAPaCa-2, and suppressed the expression of Vimentin, Snail, and increased E-cadherin expression, showing inhibition in EMT.
The suppression of Snail is due to accelerated mRNA decay.
Overexpression of HuR protected mRNA of Snail from degradation, suggesting that Snail is a direct target of HuR.
Knockdown of HuR also decreased pancreatic cancer spheroids formation.
St-3 inhibited the proliferation of pancreatic cancer cell lines more potently in HuR-high cells MIAPaCa-2 (IC50 ∼2 μM), than in HuR-low cells BxPc-3 and PANC-1 (IC50 6-20 μM).
St-3 directly bound to HuR, and inhibited binding of HuR with its target mRNAs.
St-3 treatment mimicked the HuR knockdown effects in inhibiting cell migration, EMT, and spheroids formation.
Conclusion
HuR is an important regulator in pancreatic cancer EMT and CSCs.
ST-3 as a novel HuR inhibitor inhibited pancreatic cancer EMT and CSCs.
Further investigation is under way.
Citation Format: Ruochen Dong, Kishore Polireddy, Ying Zhang, Qi Chen.
Inhibiting HuR, a RNA-binding protein, for inhibition of pancreatic cancer EMT and CSCs.
[abstract].
In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA.
Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 1610.
Related Results
7
th
International Symposium on Enabling Technologies for Life Sciences (ETP)
7
th
International Symposium on Enabling Technologies for Life Sciences (ETP)
The seventh in the series of ETP Symposia (see
Rapid Communications in Mass Spectrometry
2012,
26
, ...
Abstract 2005: CSCs induced from iPSCs indicate the trace of cancer cell culture conditioned media
Abstract 2005: CSCs induced from iPSCs indicate the trace of cancer cell culture conditioned media
Abstract
Cancer stem cells (CSCs) show drug resistance and could be a source of cancer cells. Although these cells are recently considered more important than ever i...
Markers and Reporters to Reveal the Hierarchy in Heterogeneous Cancer Stem Cells
Markers and Reporters to Reveal the Hierarchy in Heterogeneous Cancer Stem Cells
A subpopulation within cancer, known as cancer stem cells (CSCs), regulates tumor initiation, chemoresistance, and metastasis. At a closer look, CSCs show functional heterogeneity ...
CMLD-2 Attenuates Myofibroblast Activation and Bleomycin-Induced Pulmonary Fibrosis in Mice through Antagonizing ELAVL1-Mediated Osteopontin mRNA Stabilization
CMLD-2 Attenuates Myofibroblast Activation and Bleomycin-Induced Pulmonary Fibrosis in Mice through Antagonizing ELAVL1-Mediated Osteopontin mRNA Stabilization
Abstract
Background
Fibroblast-myofibroblasts transition (FMT) is one of the hallmark cellular processes in pulmonary fibrosis....
Cancer stem cell isolation and characterization from lung cancer cells
Cancer stem cell isolation and characterization from lung cancer cells
Lung cancer is one of the most common cancers in the world and a leading cause of death. Cancer stem cells (CSCs) are the cells responsible for tumor initiation. CSCs features inc...
Abstract 1491: Downregulation of KLF5 contributes to TGF-β- and EGF-induced EMT by reducing miR-200s.
Abstract 1491: Downregulation of KLF5 contributes to TGF-β- and EGF-induced EMT by reducing miR-200s.
Abstract
Krüpple-like factor 5 (KLF5) is a basic transcriptional factor that has been well documented for its regulatory role in the proliferation and survival of e...
Expressions of HuR, Methyl-HuR and Phospho-HuR in Endometrial Endometrioid Adenocarcinoma Are Associated with Clinical Features
Expressions of HuR, Methyl-HuR and Phospho-HuR in Endometrial Endometrioid Adenocarcinoma Are Associated with Clinical Features
HuR regulates cytoplasmic mRNA stability and translatability, with its expression correlating with adverse outcomes in various cancers. This study aimed to assess the prognostic va...
Hypoxia-driven mobilization of altruistic cancer stem cells in platinum-treated head and neck cancer
Hypoxia-driven mobilization of altruistic cancer stem cells in platinum-treated head and neck cancer
BackgroundHead and neck cancers harbor dormant cancer stem cells (CSCs). This study explores how platinum therapy impacts these cells in a non-genetic manner and the role of hypoxi...

