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Updated: Nov 30, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Effects and mechanism of microRNA‑218 against lung cancer
Yan Chen1, Ji-Lin Yang2, Zhen-Zhen Xue1
1School of Life Sciences, Yunnan University, Kunming, Yunnan 650091, P.R. China.
Abstract:
Lung cancer is the most prevalent and observed type of cancer in Xuanwei County, Yunnan, South China. Lung cancer in this area is called Xuanwei lung cancer. However, its pathogenesis remains largely unknown. To date, a number of studies have shown that microRNA (miR)‑218 functions as a tumor suppressor in multiple types of cancer. However, the role of miR‑218 and its regulatory gene network in Xuanwei lung cancer have yet to be investigated. The current study identified that the expression levels of miR‑218 in XWLC‑05 cells were markedly lower compared with those in immortalized lung epithelial BEAS‑2B cells. The present study also demonstrated that overexpression of miR‑218 could decrease cell proliferation, invasion, viability and migration in Xuanwei lung cancer cell line XWLC‑05 and NSCLC cell line NCI‑H157. Additionally, the results revealed that overexpression of miR‑218 could induce XWLC‑05 and NCI‑H157 cell apoptosis by arresting the cell cycle at G2/M phase. Finally, the present study demonstrated that overexpression of miR‑218 could lead to a significant increase in phosphatase and tensin homolog (PTEN) and YY1 transcription factor (YY1), and a decrease in B‑cell lymphoma 2 (BCL‑2) and BMI1 proto‑oncogene, polycomb ring finger (BMI‑1) at the mRNA and protein level in XWLC‑05 and NCI‑H157 cell lines. However, we did not observe any remarkable difference in the roles of miR‑218 and miR‑218‑mediated regulation of BCL‑2, BMI‑1, PTEN and YY1 expression in the progression of Xuanwei lung cancer. In conclusion, miR‑218 could simultaneously suppress cell proliferation and tumor invasiveness and induce cell apoptosis by increasing PTEN and YY1 expression, while decreasing BCL‑2 and BMI‑1 in Xuanwei lung cancer. The results demonstrated that miR‑218 might serve a vital role in tumorigenesis and progression of Xuanwei lung cancer and overexpression of miR‑218 may be a novel approach for the treatment of Xuanwei lung cancer.
Insights
MicroRNA-218 acts as a tumor suppressor in Xuanwei lung cancer by inhibiting cell proliferation and invasion. Overexpression of miR-218 shows potential as a novel therapeutic strategy for this specific lung cancer subtype.
Area of Science:
- Molecular Oncology
- Cancer Genomics
- Biomarkers in Cancer
Background:
- Xuanwei lung cancer, prevalent in Yunnan, China, has an unknown pathogenesis.
- MicroRNA (miR)-218 is recognized as a tumor suppressor in various cancers.
- The specific role of miR-218 in Xuanwei lung cancer remains uninvestigated.
Purpose of the Study:
- To investigate the role and regulatory network of miR-218 in Xuanwei lung cancer.
- To determine the effect of miR-218 overexpression on cancer cell behavior.
- To identify downstream targets regulated by miR-218 in this cancer type.
Main Methods:
- Compared miR-218 expression levels in Xuanwei lung cancer cells (XWLC-05) versus normal lung epithelial cells (BEAS-2B).
- Overexpressed miR-218 in XWLC-05 and non-small cell lung cancer (NSCLC) NCI-H157 cell lines.
- Assessed effects on cell proliferation, invasion, viability, migration, and apoptosis.
- Analyzed mRNA and protein levels of PTEN, YY1, BCL-2, and BMI-1.
Main Results:
- miR-218 expression was significantly lower in Xuanwei lung cancer cells.
- miR-218 overexpression reduced proliferation, invasion, viability, and migration.
- Overexpression induced apoptosis by arresting the cell cycle at G2/M phase.
- miR-218 increased PTEN and YY1, while decreasing BCL-2 and BMI-1 expression.
Conclusions:
- miR-218 suppresses proliferation and invasion, and induces apoptosis in Xuanwei lung cancer.
- This occurs via modulation of PTEN, YY1, BCL-2, and BMI-1 expression.
- miR-218 plays a vital role in Xuanwei lung cancer tumorigenesis and progression.
- Overexpression of miR-218 presents a potential novel therapeutic strategy.
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