Back to Search
Start Over
Raptor mediates the selective inhibitory effect of cardamonin on RRAGC-mutant B cell lymphoma.
- Source :
- BMC Complementary Medicine & Therapies; 9/26/2023, Vol. 23 Issue 1, p1-11, 11p, 1 Diagram, 7 Graphs
- Publication Year :
- 2023
-
Abstract
- Background: mTORC1 (mechanistic target of rapamycin complex 1) is associated with lymphoma progression. Oncogenic RRAGC (Rag guanosine triphosphatase C) mutations identified in patients with follicular lymphoma facilitate the interaction between Raptor (regulatory protein associated with mTOR) and Rag GTPase. It promotes the activation of mTORC1 and accelerates lymphomagenesis. Cardamonin inhibits mTORC1 by decreasing the protein level of Raptor. In the present study, we investigated the inhibitory effect and possible mechanism of action of cardamonin in RRAGC-mutant lymphoma. This could provide a precise targeted therapy for lymphoma with RRAGC mutations. Methods: Cell viability was measured using a cell counting kit-8 (CCK-8) assay. Protein expression and phosphorylation levels were determined using western blotting. The interactions of mTOR and Raptor with RagC were determined by co-immunoprecipitation. Cells overexpressing RagC wild-type (RagC<superscript>WT</superscript>) and RagC Thr90Asn (RagC<superscript>T90N</superscript>) were generated by lentiviral infection. Raptor knockdown was performed by lentivirus-mediated shRNA transduction. The in vivo anti-tumour effect of cardamonin was assessed in a xenograft model. Results: Cardamonin disrupted mTOR complex interactions by decreasing Raptor protein levels. RagC<superscript>T90N</superscript> overexpression via lentiviral infection increased cell proliferation and mTORC1 activation. The viability and tumour growth rate of RagC<superscript>T90N</superscript>-mutant cells were more sensitive to cardamonin treatment than those of normal and RagC<superscript>WT</superscript> cells. Cardamonin also exhibited a stronger inhibitory effect on the phosphorylation of mTOR and p70 S6 kinase 1 in RagC<superscript>T90N</superscript>-mutant cells. Raptor knockdown abolishes the inhibitory effects of cardamonin on mTOR. An in vivo xenograft model demonstrated that the RagC<superscript>T90N</superscript>-mutant showed significantly higher sensitivity to cardamonin treatment. Conclusions: Cardamonin exerts selective therapeutic effects on RagC<superscript>T90N</superscript>-mutant cells. Cardamonin can serve as a drug for individualised therapy for follicular lymphoma with RRAGC mutations. [ABSTRACT FROM AUTHOR]
- Subjects :
- STATISTICS
GENETIC mutation
MEDICINAL plants
FLAVONOIDS
IN vivo studies
XENOGRAFTS
CELL culture
ONCOGENES
PHOSPHOTRANSFERASES
GROWTH factors
CYTOMETRY
WESTERN immunoblotting
ANIMAL experimentation
ONE-way analysis of variance
B cell lymphoma
MTOR inhibitors
ANTINEOPLASTIC agents
PRECIPITIN tests
HYDROLASES
CELL survival
GENE expression
RESEARCH funding
PLANT extracts
IRON regulatory proteins
BIOLOGICAL assay
DATA analysis software
DATA analysis
PHOSPHORYLATION
MICE
PHARMACODYNAMICS
Subjects
Details
- Language :
- English
- ISSN :
- 26627671
- Volume :
- 23
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- BMC Complementary Medicine & Therapies
- Publication Type :
- Academic Journal
- Accession number :
- 172329557
- Full Text :
- https://doi.org/10.1186/s12906-023-04166-7