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CircRNA RNA hsa_circ_0008234 Promotes Colon Cancer Progression by Regulating the miR-338-3p/ETS1 Axis and PI3K/AKT/mTOR Signaling
SIMPLE SUMMARY: Circular RNAs (circRNAs) exert an important role in cancer progression. Meanwhile, considering its widespread regulatory effect and the potential of noninvasive testing, understanding the role of circRNA in cancer is particularly meaningful. Our study identified the circRNA hsa_circ_...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093195/ https://www.ncbi.nlm.nih.gov/pubmed/37046729 http://dx.doi.org/10.3390/cancers15072068 |
Sumario: | SIMPLE SUMMARY: Circular RNAs (circRNAs) exert an important role in cancer progression. Meanwhile, considering its widespread regulatory effect and the potential of noninvasive testing, understanding the role of circRNA in cancer is particularly meaningful. Our study identified the circRNA hsa_circ_0008234 in colon cancer based on an open-accessed circRNAs expression profile. Moreover, we found that hsa_circ_0008234 could promote proliferation, invasion, and migration abilities of colon cancers, which was partly dependent on the competitive endogenous RNA mechanism (miR-338-3p/ETS1 axis). Meanwhile, we discovered that PI3K/AKT/mTOR signaling is the downstream pathway of the has_circ_0008234/miR-338-3p/ETS1 axis, which improves the effect network of circRNAs in colon cancer. ABSTRACT: Circular RNAs (circRNAs) have been shown to play a crucial role in cancer occurrence and progression. This present work investigated the link between hsa_circ_0008234 and colon cancer. Data retrieved from GSE172229 was used to compare the circRNA profiles of colon cancer and surrounding non-tumorous tissues. The amount of RNA and protein in the molecules was determined using quantitative real-time PCR (qRT-PCR) and Western blot analysis, respectively. The cell proliferation ability was assessed using CCK8, EdU, colon formation, and nude mice tumorigenesis tests. Cell invasion and migration abilities were evaluated using transwell wound healing and mice lung metastasis model. Hsa_circ_0008234 piqued our interest because bioinformatics and qRT-PCR analyses revealed that it is upregulated in colon cancer tissue. Cell phenotypic studies suggest that hsa_circ_0008234 may significantly increase colon cancer cell aggressiveness. Mice experiments revealed that inhibiting hsa_circ_0008234 significantly reduced tumor growth and metastasis. Moreover, the fluorescence in situ hybridization experiment demonstrated that hsa_circ_0008234 is primarily found in the cytoplasm, implying that it potentially functions via a competitive endogenous RNA pathway. These findings indicated that hsa_circ_0008234 may act as a “molecular sponge” for miR-338-3p, increasing the expression of miR-338-target 3p’s ETS1. In addition, the traditional oncogenic pathway PI3K/AKT/mTOR signaling was found to be the potential downstream pathway of the hsa_circ_0008234/miR-338-3p/ETS1 axis. In conclusion, hsa_circ_0008234 increases colon cancer proliferation, infiltration, and migration via the miR-338-3p/ETS1/PI3K/AKT axis; therefore, it could serve as a target and a focus for colon cancer therapy. |
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