» Articles » PMID: 30697072

MNX1-AS1 is a Functional Oncogene That Induces EMT and Activates the AKT/mTOR Pathway and MNX1 in Breast Cancer

Overview
Publisher Dove Medical Press
Specialty Oncology
Date 2019 Jan 31
PMID 30697072
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: lncRNAs have recently been identified as key regulators of basic biological processes as well as the pathogenesis of various diseases. Previous studies have shown that lncRNA MNX1-AS1 promotes cell migration and invasion in ovarian cancer; however, its role in regulating breast cancer-associated biological processes remains unclear.

Materials And Methods: We obtained paired specimens of breast cancer tissues and adjacent normal tissues by modified radical mastectomy from 36 patients, in addition to four breast cancer cell lines (MDA-MB-231, MDA-MB-468, BT-549 and MCF-7). RNA was isolated from these tissues and cell lines and subsequently subjected to quantitative real-time polymerase chain reaction. This was followed by bisulfite deep sequencing. The cells were also transfected with siRNA against MNX1-AS1. The cells were then subject to cell proliferation, Transwell migration and invasion assays. Finally, Western blotting analysis was conducted to determine expression levels of MNX1, 5-cadherin, Snail and Slug.

Results: Our results show that MNX1-AS1 expression was significantly higher in breast cancer tissues than adjacent normal tissues. Moreover, knockdown/overexpression of MNX1-AS1 inhibits/promotes proliferation, migration and invasion of breast cancer cells. MNX1-AS1 and its natural sense transcript MNX1 are expressed synergistically in breast tumor tissues. Our results suggest that MNX1-AS1 is a functional oncogene that induces epithelial-mesenchymal transition, in addition to activating AKT/mTOR pathway and its natural sense transcript MNX1 in breast cancer cells.

Conclusion: Our data indicate that MNX1-AS1 can serve as a novel therapeutic target in breast cancer.

Citing Articles

Molecular landscape of congenital vertebral malformations: recent discoveries and future directions.

Szoszkiewicz A, Bukowska-Olech E, Jamsheer A Orphanet J Rare Dis. 2024; 19(1):32.

PMID: 38291488 PMC: 10829358. DOI: 10.1186/s13023-024-03040-0.


PI3K/Akt signalling pathway-associated long noncoding RNA signature predicts the prognosis of laryngeal cancer patients.

Nie Q, Cao H, Yang J, Liu T, Wang B Sci Rep. 2023; 13(1):14764.

PMID: 37679508 PMC: 10485045. DOI: 10.1038/s41598-023-41927-3.


Metformin and long non-coding RNAs in breast cancer.

Gholami M, Klashami Z, Ebrahimi P, Mahboobipour A, Farid A, Vahidi A J Transl Med. 2023; 21(1):155.

PMID: 36849958 PMC: 9969691. DOI: 10.1186/s12967-023-03909-x.


MNX1-AS1, a c-Myc induced lncRNA, promotes the Warburg effect by regulating PKM2 nuclear translocation.

Wu Y, Wang Y, Yao H, Li H, Meng F, Li Q J Exp Clin Cancer Res. 2022; 41(1):337.

PMID: 36476366 PMC: 9727912. DOI: 10.1186/s13046-022-02547-3.


LncRNA MNX1-AS1 contributes to lung adenocarcinoma progression by targeting the miR-34a/SIRT1 axis.

Liu G, Zhang Y, Zhang X, Liu Y, Xu Y, Cui S Am J Transl Res. 2022; 14(7):4977-4989.

PMID: 35958481 PMC: 9360842.


References
1.
Mamane Y, Petroulakis E, LeBacquer O, Sonenberg N . mTOR, translation initiation and cancer. Oncogene. 2006; 25(48):6416-22. DOI: 10.1038/sj.onc.1209888. View

2.
Franke T . PI3K/Akt: getting it right matters. Oncogene. 2008; 27(50):6473-88. DOI: 10.1038/onc.2008.313. View

3.
Laplante M, Sabatini D . mTOR signaling at a glance. J Cell Sci. 2009; 122(Pt 20):3589-94. PMC: 2758797. DOI: 10.1242/jcs.051011. View

4.
Zoncu R, Efeyan A, Sabatini D . mTOR: from growth signal integration to cancer, diabetes and ageing. Nat Rev Mol Cell Biol. 2010; 12(1):21-35. PMC: 3390257. DOI: 10.1038/nrm3025. View

5.
Yecies J, Manning B . mTOR links oncogenic signaling to tumor cell metabolism. J Mol Med (Berl). 2011; 89(3):221-8. DOI: 10.1007/s00109-011-0726-6. View