Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/60045
Title: The Role of the Neat1/Mir410-3p Axis in the Invasion of Breast Cancer Cells
Authors: Dogan, Cihangir
Acikbas, Ibrahim
Urganci, Buket Er
Azizi, Zahra
Keywords: Breast Cancer
Invasion
Metastasis
Neat1
Mir-410-3P
Publisher: Elsevier
Abstract: Breast cancer, which is the most common cancer among women in T & uuml;rkiye and throughout the world, is also one of the leading causes of cancer-related deaths. A significant factor in these deaths is metastatic breast cancer, which spreads to distant organs. The metastasis of the breast tumor follows a series of steps. Many proteins and signal molecules are in charge of these processes. In addition, NEAT1, a long noncoding RNA (lncRNA), was reported to play a key role in breast cancer cell proliferation and survival. Numerous cancer kinds were also shown to have extraordinary miR-410-3p expression levels. NEAT1 and miR-410-3p expression patterns in MCF7 and MCF-10A cell lines were investigated using quantitative real-time polymerase chain reaction (qRT-PCR) in this study. The results demonstrated that NEAT1 was elevated by 2.30-fold in cancer cells in comparison to normal cells, whereas miR-410-3p was diminished by -2.85-fold. Furthermore, the transwell invasion experiment demonstrated the invasive potential of the MCF-7 cell line, whereas the MCF-10A cells could not invade. The target analysis revealed that functions of the targets were associated with biological adhesion and cel growth. In conclusion, a correlation was found between overexpression of NEAT1 and increased invasiveness of target cells, as well as inhibition of miR-410-3p, which is a regulatory target of NEAT1.
URI: https://doi.org/10.1016/j.gene.2025.149379
https://hdl.handle.net/11499/60045
ISSN: 0378-1119
1879-0038
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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