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Hsa_circ_0053063 inhibits breast cancer cell proliferation via hsa_circ_0053063/hsa-miR-330-3p/PDCD4 axis
- Source :
- Aging (Albany NY)
- Publication Year :
- 2021
- Publisher :
- Impact Journals, LLC, 2021.
-
Abstract
- Breast cancer (BC) is one of the most common malignancies and its mortality is the highest among females. Circular RNAs (circRNAs), a novel group of non-coding RNAs, play an important regulatory role in angiogenesis and cancer progression. Hsa_circ_0053063 is a circRNA generated from several exons of HADHA. The potential role of hsa_circ_0053063 in BC remains unknown and needs to be explored. Hsa_circ_0053063 was mainly located in the cytoplasm and activated in BC tissues and cell lines. The binding position between hsa_circ_0053063 and miR-330-3p was confirmed by luciferase reporter assay. Moreover, hsa_circ_0053063 inhibited cell viability, proliferation, and progression of BC through the negative regulation of miR-330-3p. Programmed cell death 4 (PDCD4) is a direct target of miR-330-3p. Besides, the over-expression of miR-330-3p promoted cell progression by directly targeting and regulating PDCD4. Mechanistically, hsa_circ_0053063 activated PDCD4 by targeting miR-330-3p to inhibit BC progression. In conclusion, hsa_circ_0053063 inhibits breast cancer cell proliferation via hsa_circ_0053063/hsa-miR-330-3p/PDCD4 axis, which may provide a new therapeutic target for BC patients.
- Subjects :
- Aging
Programmed cell death
Angiogenesis
Cell
Breast Neoplasms
breast cancer
Cell Line, Tumor
hsa-miR-330-3p
medicine
Humans
Viability assay
Cell Proliferation
PDCD4
Chemistry
Competing endogenous RNA
RNA-Binding Proteins
Cancer
ceRNA
RNA, Circular
Cell Biology
medicine.disease
Gene Expression Regulation, Neoplastic
MicroRNAs
medicine.anatomical_structure
Cytoplasm
Cell culture
HADH
Cancer research
Female
hsa_circ_0053063
Apoptosis Regulatory Proteins
Research Paper
Subjects
Details
- ISSN :
- 19454589
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- Aging
- Accession number :
- edsair.doi.dedup.....4c3dab68583fbe469db5bbba2d755b5e
- Full Text :
- https://doi.org/10.18632/aging.202707