Identification of melanoma-specific exosomal miRNAs as the potential biomarker for canine oral melanoma.
Al Asmaul HusnaMd Mahfuzur RahmanYu-Chang LaiHui-Wen ChenM D Nazmul HasanTakayuki NakagawaNaoki MiuraPublished in: Pigment cell & melanoma research (2021)
Considering the importance of the canine cancer model of human disease, as well as the need for strategies for canine cancer management, the properties of exosomes are an emerging topic in canine oncology. In our study, exosomal RNA was isolated and investigated by next-generation sequencing. We identified several differentially expressed microRNAs (miRNAs/miRs) in the exosomes of two melanoma cell lines compared with non-tumor reference exosomes. We explored these potential melanoma-specific exosomal miRNAs further and found that miR-143 and let-7b increased in primary, whereas miR-210, 708, 221, and 222 increased in metastatic site originated melanoma cells. Further analysis showed miR-143 and 221 significantly increased in plasma exosomes of metastatic melanoma patients. Moreover, the sensitivity and specificity are >85% for differentiating the non-metastatic and metastatic patients. Therefore, these miRNAs can be an incredible biomarker candidate to identify metastatic melanoma and facilitate a better prognosis.
Keyphrases
- mesenchymal stem cells
- cell proliferation
- end stage renal disease
- stem cells
- long non coding rna
- small cell lung cancer
- squamous cell carcinoma
- ejection fraction
- newly diagnosed
- chronic kidney disease
- long noncoding rna
- papillary thyroid
- magnetic resonance imaging
- endothelial cells
- peritoneal dialysis
- dna methylation
- skin cancer
- computed tomography
- squamous cell
- young adults
- copy number
- lymph node metastasis
- patient reported
- childhood cancer
- pluripotent stem cells
- cell free