التفاصيل البيبلوغرافية
| العنوان: |
Exosomal miR-182 derived from bone marrow mesenchymal stem cells drives carfilzomib resistance of multiple myeloma cells by targeting SOX6. |
| المؤلفون: |
Long, Shifeng, Long, Shengping, He, Honglei, Luo, Liang, Liu, Mei, Ding, Ting |
| المصدر: |
Journal of Orthopaedic Surgery & Research; 12/7/2023, Vol. 18 Issue 1, p1-14, 14p |
| مصطلحات موضوعية: |
THERAPEUTIC use of protease inhibitors, THERAPEUTIC use of antineoplastic agents, REVERSE transcriptase polymerase chain reaction, EXOSOMES, PROTEASE inhibitors, WESTERN immunoblotting, CANCER invasiveness, MICRORNA, MOLECULAR pathology, METASTASIS, CANCER patients, GENE expression, CELL motility, CELL proliferation, MULTIPLE myeloma, CELL lines, TRANSCRIPTION factors, MESENCHYMAL stem cells, DRUG resistance in cancer cells, PHARMACODYNAMICS |
| مستخلص: |
Background: Multiple myeloma (MM) is a common hematological malignancy. Drug resistance remains to be a major clinical challenge in MM therapy. In this study, we aim to investigate the functional roles of bone marrow mesenchymal stem cells (BMSC)-derived exosomal miR-182 on the carfilzomib resistance of MM and its underlying mechanism. Methods: qRT-PCR and Western blot methods were utilized to confirm the gene or protein expressions. CCK-8 and transwell assays were performed to measure the capabilities of proliferation, migration, and invasion. The molecular interactions were validated through ChIP and Dual luciferase assay. Results: Our findings indicated that miR-182 expression was upregulated in serum, BMSCs and BMSC-derived exosomes from MM patients. Hypoxia-inducible factor-1α (HIF-1α), a key transcriptional factor in tumor microenvironment, could boost miR-182 expression by directly binding to its promoter, thus favoring exosomal secretion. Moreover, exosomal miR-182 from BMSCs could be transferred to MM cells and was able to promote malignant proliferation, metastasis, and invasion, as well as decrease the sensitivity of MM cells against carfilzomib. Additionally, SOX6 was identified as a downstream target of miR-182 in MM cells, and its expression was negatively regulated by miR-182. Rescue experiments proved that loss of SOX6 in MM cells dramatically reversed the promoting roles of BMSC-secreted exosomal miR-182 on proliferation, metastasis, and carfilzomib resistance in MM cells. Conclusion: Collectively, our findings indicated that exosomal miR-182 derived from BMSCs contributed to the metastasis and carfilzomib resistance of MM cells by targeting SOX6. This study sheds light on the pathogenesis of the BMSC-derived exosome containing miR-182 in the malignant behaviors of MM cells and carfzomib resistance. Highlights: miR-182 is greatly elevated in serum, BMSCs, and BMSCs-exosomes derived from MM patients. HIF-1α binds to miR-182 promotor to activate its transcription and exosome secretion in BMSCs. SOX6 is a downstream target of miR-182 and is negatively regulated by miR-182. Exosomal miR-182 secreted by BMSCs promotes MM cell proliferation, metastasis, and carfilzomib resistance by targeting SOX6. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |
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