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Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
Published on: June 9, 2023
tRF-22-WE8SPOX52 promotes progression of breast cancer by down-regulating MAP2K4
Yuqi Fu1, Huanhuan Hu2, Dandan Wang3
1Department of Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, 210009, China.
Abstract:
tsRNAs are a novel class of non-coding RNAs. The functions of tsRNAs in breast cancer are still not largely understood. In the present study, we detected expression of tsRNAs in both serum-derived exosomes and breast tumors, and explored the roles of the differentially expressed tsRNAs. We profiled tsRNAs in serum-derived exosomes from breast cancer patients, and explored the functions and mechanisms of tsRNAs via bioinformatics methods, RT-qPCR, transwell assay, cell counting kit-8 assay, colony formation assay, wound healing assay, cell cycle analysis, apoptosis assay, dual-Luciferase reporter assay, and western blot. We identified 34 differentially expressed tsRNAs in serum-derived exosomes. After validation in 15 paired tissues and 80 serums using RT-qPCR and identified tRF-22-WE8SPOX52 as an up-regulated tsRNA. The area under curve for exosomal tRF-22-WE8SPOX52 was 0.859. The overexpression of tRF-22-WE8SPOX52 promoted cell proliferation, migration, and invasion of BC cells while suppressing apoptosis. Similarly, knockdown of tRF-22-WE8SPOX52 also confirmed its effects. Western blot assay and dual luciferase assay showed MAP2K4 is a target of tRF-22-WE8SPOX52. tRF-22-WE8SPOX52 promotes BC by suppressing MAP2K4. tRF-22-WE8SPOX52 is significantly up-regulated in serum-derived exosomes and tumors from breast cancer patients. Exosomal tRF-22-WE8SPOX52 may serve as a potential biomarker for breast cancer.
Insights
Small tumor RNA fragments (tsRNAs) are implicated in breast cancer progression. Exosomal tsRNA tRF-22-WE8SPOX52 promotes cancer cell growth and invasion by targeting MAP2K4, suggesting its potential as a breast cancer biomarker.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Small tumor RNA fragments (tsRNAs) represent a novel class of non-coding RNAs.
- The specific roles of tsRNAs in breast cancer (BC) pathogenesis remain largely unelucidated.
- Investigating tsRNA expression in serum-derived exosomes and tumor tissues is crucial for understanding their involvement in BC.
Purpose of the Study:
- To profile tsRNA expression in serum-derived exosomes from breast cancer patients.
- To explore the functional roles and underlying mechanisms of differentially expressed tsRNAs in BC.
- To identify potential tsRNA biomarkers for breast cancer detection.
Main Methods:
- tsRNA profiling in exosomes, bioinformatics analysis, RT-qPCR, Transwell assays, CCK-8, colony formation, wound healing assays, cell cycle and apoptosis analyses.
- Dual-luciferase reporter assays and Western blotting were employed to elucidate molecular mechanisms.
- Validation was performed in paired tumor tissues and patient serum samples.
Main Results:
- Thirty-four differentially expressed tsRNAs were identified in serum-derived exosomes.
- Exosomal tRF-22-WE8SPOX52 was validated as significantly up-regulated in BC patients' serum and tumors (AUC=0.859).
- Overexpression of tRF-22-WE8SPOX52 promoted BC cell proliferation, migration, and invasion, while inhibiting apoptosis, by suppressing MAP2K4.
Conclusions:
- tRF-22-WE8SPOX52 promotes breast cancer progression by downregulating MAP2K4.
- Exosomal tRF-22-WE8SPOX52 demonstrates significant up-regulation in breast cancer.
- Exosomal tRF-22-WE8SPOX52 holds promise as a potential diagnostic biomarker for breast cancer.
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