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Long non-coding RNA TMPO-AS1 promotes tumor progression via sponging miR-140-5p in breast cancer
Dandan Zhu1, Weize Lv2, Xiao Zhou3
1Department of Medical Oncology, The Third Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150040, P.R. China.
Abstract:
Long non-coding RNAs (lncRNAs) are involved in carcinogenesis and tumor suppression, and are novel biological tumor regulators. However, the functional roles of lncRNAs and their underlying dysregulation mechanisms in breast cancer are not completely understood. The aim of the present study was to investigate the clinical significance and biological functions of lncRNA TMPO antisense RNA 1 (TMPO-AS1) in breast cancer. TMPO-AS1 levels were measured in human cancer tissues and breast cancer cell lines, and the functional roles of TMPO-AS1 in breast cancer cells were investigated by performing in vitro and in vivo assays. Additionally, luciferase reporter assays were conducted to detect the association between microRNA (miR)-140-5p and TMPO-AS1. TMPO-AS1 expression levels were significantly increased in breast cancer tissues and cell lines compared with adjacent non-cancerous tissues and MCF-10A cells, respectively. In vitro and in vivo studies indicated that TMPO-AS1 knockdown significantly suppressed breast cancer cell viability at 48 and 72 h compared with the small interfering (si)RNA negative control group (NC; siNC). TMPO-AS1 knockdown in vitro inhibited MCF-7 and T47D cell migration and invasion compared with the siNC group. TMPO-AS1 knockdown in metastatic breast cancer cells also decreased metastatic colonization in the mouse lung compared with the short hairpin RNA NC group. Mechanistically, TMPO-AS1 promoted cellular viability and migration as a competing endogenous RNA by sponging miR-140-5p. The results suggested that TMPO-AS1 may serve as a potential therapeutic target in patients with breast cancer.
Insights
Long non-coding RNA TMPO-AS1 is upregulated in breast cancer and promotes tumor growth and metastasis. Inhibiting TMPO-AS1 suppressed cancer cell viability and invasion, suggesting it as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) are emerging regulators in cancer development.
- The specific roles of lncRNAs, like TMPO-AS1, in breast cancer remain largely undefined.
- Understanding lncRNA dysregulation is crucial for identifying novel therapeutic targets.
Purpose of the Study:
- To investigate the clinical significance and biological functions of lncRNA TMPO antisense RNA 1 (TMPO-AS1) in breast cancer.
- To explore the underlying molecular mechanisms of TMPO-AS1 in breast cancer progression.
- To assess TMPO-AS1 as a potential therapeutic target for breast cancer.
Main Methods:
- Quantification of TMPO-AS1 expression in breast cancer tissues and cell lines.
- In vitro and in vivo assays to evaluate the functional impact of TMPO-AS1 knockdown.
- Luciferase reporter assays to determine the interaction between TMPO-AS1 and miR-140-5p.
Main Results:
- TMPO-AS1 expression was significantly elevated in breast cancer tissues and cell lines.
- TMPO-AS1 knockdown reduced breast cancer cell viability, migration, and invasion in vitro.
- TMPO-AS1 knockdown decreased metastatic colonization in vivo and acts as a competing endogenous RNA by sponging miR-140-5p.
Conclusions:
- TMPO-AS1 plays a significant role in promoting breast cancer cell viability and metastasis.
- TMPO-AS1 functions by sponging miR-140-5p, acting as a competing endogenous RNA.
- TMPO-AS1 represents a promising therapeutic target for breast cancer treatment.
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