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MicroRNA Based Liquid Biopsy: The Experience of the Plasma miRNA Signature Classifier MSC for Lung Cancer Screening
Published on: October 26, 2017
Circulating Interleukins as Biomarkers in Non-Small Cell Lung Cancer Patients: A Pilot Study Compared to Normal
Wei-Wen Lim1,2, Jason H Leung3, Chen Xie1
1National Heart Research Institute of Singapore, National Heart Center Singapore, Singapore 169609, Singapore.
Interleukin-11 shows potential as a biomarker for non-small cell lung cancer (NSCLC) in plasma, but detection challenges remain for other interleukins and sample types. Further research is needed to optimize biomarker assays.
Area of Science:
- Oncology
- Biochemistry
- Molecular Biology
Background:
- Biomarkers are crucial for non-small cell lung cancer (NSCLC) diagnosis and patient stratification.
- Interleukins (ILs) are investigated as potential NSCLC biomarkers.
- Exhaled-breath condensates (EBCs) offer a non-invasive sampling option.
Purpose of the Study:
- To evaluate IL-11, IL-6, IL-8, IL-17A, and IL-33 as biomarkers in NSCLC.
- To compare biomarker levels in NSCLC patients' plasma, sera, and EBCs against healthy controls.
- To validate findings in NSCLC tumor tissues.
Main Methods:
- Conventional ELISA and high-sensitivity PCR-based ELISA were used to measure interleukin levels.
- RT-qPCR and immunohistochemistry were employed for gene and protein validation.
- Plasma, sera, and EBCs from NSCLC patients and healthy volunteers were analyzed.
Main Results:
- IL-11 was significantly elevated in NSCLC patient plasma compared to controls (p < 0.0001).
- IL-11 was undetectable in sera and EBCs using conventional ELISA.
- IL-11 gene and protein upregulation was confirmed in NSCLC tumors.
- IL-6, IL-8, IL-17A, and IL-33 lacked detection sensitivity, indicating a need for improved assays.
- Discrepancies were observed between paired plasma and serum biomarker concentrations.
Conclusions:
- IL-11 shows promise as a plasma biomarker for NSCLC, but detection sensitivity needs optimization.
- Current assays are insufficient for detecting IL-6, IL-8, IL-17A, and IL-33 in the studied samples.
- Caution is advised against relying on a single type of blood sample for biomarker assessment.
- Further research should focus on enhancing assay sensitivity and exploring diverse sample matrices for NSCLC biomarker discovery.
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