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Data · dataset · 2025

Sequencing of mRNA, lncRNA, and circRNA in LLC Cells Treated with Ophiopogonin D

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Lung cancer, especially non-small cell lung cancer (NSCLC), is the leading cause of cancer-related deaths worldwide.

Description

Natural products play a crucial role in drug development, and most current therapies are derived from these ingredients. Ophiopogon D (OP-D) has received widespread attention due to its broad anti-cancer properties, including the ability to inhibit cell proliferation and induce cell apoptosis. In this study, we performed whole transcriptome sequencing on LLC cells treated with OP-D. Cultivate LLC cells using standard methods and use TRIzol ® Extract total RNA using reagents.

Evaluate RNA quality using Agilent 5300 Bioanalyzer and quantify using NanoDrop ND-2000. Construct sequencing libraries using only high-quality RNA samples (OD260/280=1.8-2.2, OD260/230 ≥ 2.0, RQN ≥ 6.5, 28S: 18S ≥ 1.0,>1 μ g). We used Illumina Stranded Total RNA Prep and Ribo Zero Plus for library preparation, generating ribosomal RNA removal libraries including mRNA, lncRNA, and circRNA information.

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These libraries were sequenced on the Illumina NovaSeq Xplus platform at Majorbio in Shanghai, and a large dataset was uploaded in FASTQ format. The main findings indicate that OP-D processing resulted in significant inter group differentiation as shown in principal component analysis (PCA). Differential expression analysis showed significant downregulation of lncMALAT1, confirming MALAT1 as a significant lncRNA. In addition, mRNA analysis showed that OP-D treatment inhibited key features of malignant tumors, including metastasis and proliferation, highlighting its extensive inhibitory effect on carcinogenic processes. 

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Inferred from text
Cancer 75% · RNA sequencing 65% · Sequencing 75%
Provenance · 1 source records, 13 field assertions
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ScienceDB10.57760/sciencedb.2899810 d agoJSON v1
FieldAssertionExtractorEvidence
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