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Integrated Proteomic and Transcriptomic Analysis Reveals Long Noncoding RNA HOX Transcript Antisense Intergenic RNA
Ying Wu1,2, Qian Xiong1, Siting Li1,2
1From the ‡Key Laboratory of Algal Biology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
Abstract:
Long noncoding RNA HOX transcript antisense RNA (HOTAIR) is involved in human tumorigenesis and is dysregulated in hepatocellular carcinoma (HCC). However, the molecular mechanisms underlying HOTAIR functions in HCC are largely unknown. Here, we employed an integrated transcriptomic and quantitative proteomic analysis to systematically explore the regulatory role of HOTAIR in HCC. A total of 673 transcripts and 293 proteins were found to be dysregulated after HOTAIR inhibition. Bioinformatics studies indicated that differentially expressed genes (DEGs) and differentially expressed proteins (DEPs) are involved in many biological processes, especially cancer-related signaling pathways. A set of DEGs and DEPs were validated by quantitative RT-PCR, Western blot and parallel reaction monitoring (PRM) analysis, respectively. Further functional studies of the opioid growth factor receptor (OGFr), a negative biological regulator of cell proliferation in HCC, revealed that HOTAIR exerts its effects on cell proliferation, at least in part, through the regulation of OGFr expression. By correlating the omics data with functional studies, the current results provide novel insights into the functional mechanisms of HOTAIR in HCC cells.
Insights
Long noncoding RNA HOTAIR influences hepatocellular carcinoma (HCC) progression. This study reveals HOTAIR regulates opioid growth factor receptor (OGFr) expression, impacting cell proliferation in HCC.
Area of Science:
- Molecular Biology
- Genomics
- Proteomics
Background:
- Long noncoding RNA HOTAIR is implicated in human cancers, including hepatocellular carcinoma (HCC).
- The precise molecular mechanisms of HOTAIR in HCC remain largely unexplored.
Purpose of the Study:
- To systematically investigate the regulatory functions of HOTAIR in HCC using integrated transcriptomic and proteomic analyses.
- To elucidate the molecular pathways influenced by HOTAIR in HCC development.
Main Methods:
- Integrated transcriptomic and quantitative proteomic analysis following HOTAIR inhibition.
- Bioinformatic analysis of differentially expressed genes (DEGs) and proteins (DEPs).
- Validation using quantitative RT-PCR, Western blot, and parallel reaction monitoring (PRM).
Main Results:
- HOTAIR inhibition led to significant dysregulation of 673 transcripts and 293 proteins.
- DEGs and DEPs were enriched in cancer-related signaling pathways.
- HOTAIR regulates opioid growth factor receptor (OGFr) expression, affecting HCC cell proliferation.
Conclusions:
- This study provides novel insights into HOTAIR's functional mechanisms in HCC.
- HOTAIR's role in HCC cell proliferation is, in part, mediated by OGFr regulation.
- Integrated omics data and functional studies advance understanding of HOTAIR in HCC.
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