MSC-regulated lncRNA MACC1-AS1 promotes stemness and chemoresistance through fatty acid oxidation in gastric cancer.
Wanming HeBishan LiangChunlin WangShaowei LiYang ZhaoQiong HuangZe-Xian LiuZhiqi YaoQijing WuWangjun LiaoShuyi ZhangYajing LiuYi XiangJia LiuMin ShiPublished in: Oncogene (2019)
Chemotherapy is the preferred treatment for advanced stage gastric cancer (GC) patients and chemotherapy resistance is the major obstacle to effective cancer therapy. Increasing evidence suggests that mesenchymal stem cells (MSCs) make important contributions to development of drug resistance. However, the underlying mechanism remains elusive. In this study, we discovered that abundant MSCs in tumor tissues predicted a poor prognosis in GC patients. MSCs promoted stemness and chemoresistance in GC cells through fatty acid oxidation (FAO) in vitro and in vivo. Mechanically, transforming growth factor β1 (TGF-β1) secretion by MSCs activated SMAD2/3 through TGF-β receptors and induced long non-coding RNA (lncRNA) MACC1-AS1 expression in GC cells, which promoted FAO-dependent stemness and chemoresistance through antagonizing miR-145-5p. Moreover, pharmacologic inhibition of FAO with etomoxir (ETX) attenuated MSC-induced FOLFOX regiment resistance in vivo. These results suggest that FAO plays an important role in MSC-mediated stemness and chemotherapy resistance in GC and FAO inhibitors in combination with chemotherapeutic drugs present as a promising strategy to overcome chemoresistance.
Keyphrases
- poor prognosis
- long non coding rna
- transforming growth factor
- mesenchymal stem cells
- epithelial mesenchymal transition
- end stage renal disease
- stem cells
- umbilical cord
- fatty acid
- induced apoptosis
- cancer stem cells
- newly diagnosed
- ejection fraction
- chronic kidney disease
- cancer therapy
- gene expression
- peritoneal dialysis
- locally advanced
- gas chromatography
- squamous cell carcinoma
- drug delivery
- cell cycle arrest
- radiation therapy
- rectal cancer
- drug induced
- diabetic rats
- signaling pathway
- transcription factor
- endothelial cells
- mass spectrometry
- pi k akt