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Chemotherapy-Induced miRNA-29c/Catenin-δ Signaling Suppresses Metastasis in Gastric Cancer
- Source :
- Cancer Research. 75:1332-1344
- Publication Year :
- 2015
- Publisher :
- American Association for Cancer Research (AACR), 2015.
-
Abstract
- Chemotherapy has improved the survival of patients with gastric cancer by unknown mechanisms. In this study, we showed that cisplatin and docetaxel used in gastric cancer treatment increase the expression of miRNA-29 (miR-29) family members and decrease the expression of their oncogenic targets, mediating a significant part of the efficacious benefits of these chemotherapeutic agents. In particular, patients with gastric cancer who experienced recurrences after chemotherapy tended to exhibit low levels of miR-29c expression in their tumors, suggesting that miR-29c activation may contribute to the chemotherapeutic efficacy. Enforced expression of miR-29s in gastric cancer cells inhibited cell invasion in vitro and in vivo by directly targeting catenin-δ (CTNND1). Drug treatment suppressed gastric cancer cell invasion by restoring miR-29c–mediated suppression of catenin-δ and RhoA signaling. In parallel, drug treatment also activated several tumor-suppressive miRNAs, thereby decreasing expression of their oncogenic effector targets. Overall, our findings defined a global mechanism for understanding the efficacious effects of cytotoxic chemotherapy in gastric cancer. Cancer Res; 75(7); 1332–44. ©2015 AACR.
- Subjects :
- rho GTP-Binding Proteins
Oncology
Delta Catenin
Cancer Research
medicine.medical_specialty
Lung Neoplasms
RHOA
Gene Expression
Mice, Nude
Antineoplastic Agents
Docetaxel
Kaplan-Meier Estimate
Metastasis
Cell Movement
Stomach Neoplasms
Cell Line, Tumor
Internal medicine
medicine
Animals
Humans
Neoplasm Invasiveness
Cisplatin
biology
CTNND1
business.industry
Cancer
Catenins
medicine.disease
Gene Expression Regulation, Neoplastic
MicroRNAs
Catenin
Cancer cell
biology.protein
RNA Interference
Taxoids
business
Neoplasm Transplantation
medicine.drug
Subjects
Details
- ISSN :
- 15387445 and 00085472
- Volume :
- 75
- Database :
- OpenAIRE
- Journal :
- Cancer Research
- Accession number :
- edsair.doi.dedup.....b118b3ec438ae30022d1316d1a3e036c