Nanoliposomal Delivery of MicroRNA-203 Suppresses Migration of Triple-Negative Breast Cancer through Distinct Target Suppression.
Shuxuan SongKelsey S JohnsonHenry LujanSahar H PradhanChristie M SayesJoseph H TaubePublished in: Non-coding RNA (2021)
Triple-negative breast cancers affect thousands of women in the United States and disproportionately drive mortality from breast cancer. MicroRNAs are small, non-coding RNAs that negatively regulate gene expression post-transcriptionally by inhibiting target mRNA translation or by promoting mRNA degradation. We have identified that miRNA-203, silenced by epithelial-mesenchymal transition (EMT), is a tumor suppressor and can promote differentiation of breast cancer stem cells. In this study, we tested the ability of liposomal delivery of miR-203 to reverse aspects of breast cancer pathogenesis using breast cancer and EMT cell lines. We show that translationally relevant methods for increasing miR-203 abundance within a target tissue affects cellular properties associated with cancer progression. While stable miR-203 expression suppresses LASP1 and survivin, nanoliposomal delivery suppresses BMI1, indicating that suppression of distinct mRNA target profiles can lead to loss of cancer cell migration.
Keyphrases
- epithelial mesenchymal transition
- signaling pathway
- cell proliferation
- long non coding rna
- gene expression
- cell migration
- papillary thyroid
- long noncoding rna
- cancer stem cells
- poor prognosis
- binding protein
- childhood cancer
- squamous cell
- dna methylation
- type diabetes
- breast cancer risk
- physical activity
- cardiovascular events
- pregnant women
- risk factors
- wastewater treatment
- lymph node metastasis
- insulin resistance
- cervical cancer screening