Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 May;195(5):3096-3108.
doi: 10.1007/s12010-022-04267-y. Epub 2022 Dec 16.

lncRNA ENST00000585827 Contributes to the Progression of Endometrial Carcinoma via Regulating miR-424/E2F6/E2F7 Axis

Affiliations

lncRNA ENST00000585827 Contributes to the Progression of Endometrial Carcinoma via Regulating miR-424/E2F6/E2F7 Axis

Derong Fang et al. Appl Biochem Biotechnol. 2023 May.

Abstract

Endometrial cancer (EC) ranks fourth among the most common gynecologic malignancies. Despite advances in medical technology, the pathogenesis is still unclear. Numerous reports have identified the involvement of lncRNA in the malignant progression of endometrial cancer. The aim of the study was to investigate the expression level of lncRNA ENST00000585827 (lncRNA E27) in endometrial cancer and the molecular mechanism that regulates the development of endometrial cancer. Combined with the results of the previous study, PCR analysis confirmed that lncRNA E27 was significantly upregulated in endometrial cancer cell lines. The results of CCK-8, wound healing assay, and transwell experiments showed that lncRNA E27 could significantly inhibit cell proliferation, migration, and invasion. Flow cytometry results confirmed that lncRNA E27 could promote apoptosis. Furthermore, based on bioinformatics predictions, dual-luciferase assay and RT-qPCR analysis confirmed that miR-424, as its downstream molecule, competitively regulates the expression of E2F6/E2F7. Rescue experiments further supported that lncRNA E27 inhibited proliferation, migration, invasion, and promoted apoptosis of endometrial cancer through miR-424/E2F6/E2F7 signaling axis. Conclusively, our findings revealed the role of lncRNA E27 in regulating the miR-424/E2F6/E2F7 signaling axis during EC progression, opening up new strategies for the treatment of endometrial cancer.

Keywords: E2F6/E2F7; Endometrial carcinoma; lncRNA ENST00000585827; miR-424.

PubMed Disclaimer

References

    1. Piulats, J., et al. (2017). Molecular approaches for classifying endometrial carcinoma. Gynecologic oncology, 145(1), 200–207. - DOI - PubMed
    1. Yeramian, A., et al. (2013). Endometrial carcinoma: Molecular alterations involved in tumor development and progression. Oncogene, 32(4), 403–413. - DOI - PubMed
    1. Garg, K., & Soslow, R. (2014). Endometrial carcinoma in women aged 40 years and younger. Archives of pathology & laboratory medicine, 138(3), 335–342. - DOI
    1. Yu, W., et al. (2010). Dietary vitamin D exposure prevents obesity-induced increase in endometrial cancer in Pten+/- mice. Cancer Prevention Research (Philadelphia, Pa.), 3(10), 1246–58. - DOI - PubMed
    1. Takenaka, K., et al. (2016). The emerging role of long non-coding RNAs in endometrial cancer. Cancer genetics, 209(10), 445–455. - DOI - PubMed

MeSH terms

LinkOut - more resources