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Long Non-Coding RNA LINC01123 Facilitates Cholangiocarcinoma Aggravation by Targeting miR-641
Xueshuo Wu1, Ling Wang2, Xiaoming Wang3
1Department of General Surgery, The Second Affiliated Hospital of Guangzhou Medical University, Panyu Campus, Guangzhou, China.
Summary
Long non-coding RNA LINC01123 is upregulated in cholangiocarcinoma (CCA), promoting cancer progression by downregulating miR-641. This finding offers potential therapeutic targets for CCA treatment.
Area of Science:
- Molecular oncology
- Cancer biology
Background:
- Cholangiocarcinoma (CCA) is a challenging malignancy with limited treatment options.
- Long non-coding RNAs (LncRNAs) like LINC01123 play a role in cancer progression by regulating gene expression.
- Understanding the role of LINC01123 in CCA is crucial for developing effective therapeutic strategies.
Purpose of the Study:
- To investigate the association between LINC01123 and CCA.
- To elucidate the underlying molecular mechanism of LINC01123 in CCA progression.
- To identify LINC01123 as a potential therapeutic target for CCA management.
Main Methods:
- Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) to measure LINC01123 and miR-641 expression in 128 CCA patient samples.
- Cell counting Kit-8 (CCK-8), transwell migration, and invasion assays to assess the biological functions of LINC01123 and miR-641 in CCA cells.
- Dual luciferase reporter assays and rescue experiments to investigate the regulatory mechanism.
Main Results:
- LINC01123 expression was significantly higher in CCA tissues and cells compared to normal controls.
- LINC01123 promoted CCA cell proliferation, migration, and invasion.
- LINC01123 expression was negatively correlated with miR-641 expression, indicating LINC01123 downregulates miR-641 to drive CCA progression.
- Elevated LINC01123 levels correlated with lymph node metastasis and advanced TNM stage.
Conclusions:
- LINC01123 is upregulated in CCA and promotes tumor progression by targeting miR-641.
- LINC01123 serves as a potential diagnostic biomarker and therapeutic target for cholangiocarcinoma.
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