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Aralin, a type II ribosome-inactivating protein from Aralia elata, exhibits selective anticancer activity through the processed form of a 110-kDa high-density lipoprotein-binding protein: a promising anticancer drug
- Source :
- Biochemical and biophysical research communications. 453(1)
- Publication Year :
- 2014
-
Abstract
- Aralin from Aralia elata is a newly identified type II ribosome- inactivating protein, which preferentially induces apoptosis in cancer cells. In this study, we identified that the aralin receptor is a 110-kDa high-density lipoprotein-binding protein (HDLBP), which functions as a HDL receptor. The sensitivities of tumor cell lines to aralin were dependent on the expression levels of the 110-kDa HDLBP and its forced expression in aralin-resistant Huh7 cells conferred aralin sensitivity. HDLBP-knockdown HeLa cells showed a significant aralin resistance in vitro and in vivo. Conversely, ectopic expression of the 150-kDa HDLBP resulted in increased aralin sensitivity in vivo, accompanying enhanced expression of the 110-kDa HDLBP. Thus, these results showed that the 110-kDa HDLBP in lipid rafts acted as an aralin receptor and that its expression levels determined aralin sensitivity, suggesting that aralin could be a promising anticancer drug for HDLBP-overexpressing tumors.
- Subjects :
- Biophysics
Administration, Oral
Mice, Nude
Biology
Biochemistry
HeLa
Membrane Microdomains
Cell Line, Tumor
Animals
Humans
Receptor
Molecular Biology
Receptors, Lipoprotein
Ribosome-inactivating protein
RNA-Binding Proteins
Cell Biology
Hep G2 Cells
Aralia
biology.organism_classification
Antineoplastic Agents, Phytogenic
Xenograft Model Antitumor Assays
In vitro
Aralia elata
Recombinant Proteins
Cell biology
Molecular Weight
Ribosome Inactivating Proteins, Type 2
Apoptosis
Gene Knockdown Techniques
Cancer cell
Ectopic expression
Lipoproteins, HDL
HeLa Cells
Subjects
Details
- ISSN :
- 10902104
- Volume :
- 453
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Biochemical and biophysical research communications
- Accession number :
- edsair.doi.dedup.....348ae953b639d6d4e2e89214aa192595