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Generation and Expansion of Primary, Malignant Pleural Mesothelioma Tumor Lines
Published on: April 21, 2022
Soluble mesothelin-related peptide level elevation in mesothelioma serum and pleural effusions
Harvey I Pass1, Anil Wali, Naimei Tang
1Department of Cardiothoracic Surgery, Division of Thoracic Surgery, New York University School of Medicine, New York, New York 10016, USA. harvey.pass@med.nyu.edu
Background:
Soluble mesothelin-related peptide (SMRP) is a potential marker for malignant pleural mesothelioma (MPM), which may be useful for screening high-risk asbestos-exposed individuals.
Methods:
We evaluated SMRP in serum from MPM patients (n = 90), lung cancer patients (n = 170), age and tobacco-matched asbestos-exposed individuals (n = 66), and in MPM pleural effusions (n = 45), benign effusions (n = 30), and non-MPM effusions (n = 20) using the MesoMark enzyme-linked immunosorbent assay kit (Fujirebio Diagnostics, Malvern, PA). Receiver operating characteristic (ROC) curves were used to define true and false positive rates at various cutoffs.
Results:
Mean serum SMRP levels were higher in MPM compared with lung cancer (5.67 +/- 0.82 nM [mean +/- standard error of the mean vs 1.99 +/- 0.43 nM, p < 0.001), and stage I MPM SMRP levels (n = 12; 2.09 +/- 0.41 nM) were significantly higher than those in asbestos-exposed individuals (0.99 +/- 0.09 nM, p = 0.02, respectively). Stage 2 to 4 SMRP serum levels were significantly higher than those for stage 1 MPM. The area under the ROC curve for serum SMRP was 0.81 for differentiating MPM and asbestos-exposed individuals; cutoff = 1.9 nM (sensitivity = 60%, specificity = 89%). The MPM pleural effusion SMRP was significantly higher than benign or other non-MPM pleural effusions (65.57 +/- 11.33 nM vs 27.46 +/- 11.25 nM [p = 0.003] and 18.99 +/- 7.48 nM [p = 0.044], respectively).
Conclusions:
These data support SMRP as a promising marker for MPM in both serum and pleural effusion fluid, and justify prospective screening studies of SMRP in combination with other markers for screening of asbestos-exposed cohorts.
Insights
Soluble mesothelin-related peptide (SMRP) shows promise as a biomarker for malignant pleural mesothelioma (MPM). Elevated SMRP levels in serum and pleural fluid could aid in early detection among high-risk asbestos-exposed individuals.
Area of Science:
- Oncology
- Biomarker Discovery
- Asbestos-Related Diseases
Background:
- Malignant pleural mesothelioma (MPM) is a serious cancer linked to asbestos exposure.
- Soluble mesothelin-related peptide (SMRP) is a potential biomarker for MPM.
- Screening high-risk asbestos-exposed individuals is crucial for early detection.
Purpose of the Study:
- To evaluate the diagnostic utility of SMRP in serum and pleural effusions for MPM.
- To compare SMRP levels in MPM patients with those in lung cancer patients and asbestos-exposed individuals.
- To assess SMRP's effectiveness in differentiating MPM from other conditions.
Main Methods:
- Serum and pleural effusion samples were analyzed for SMRP using the MesoMark enzyme-linked immunosorbent assay.
- Patient groups included MPM (n=90), lung cancer (n=170), and asbestos-exposed individuals (n=66).
- Receiver operating characteristic (ROC) curves were employed to determine diagnostic accuracy.
Main Results:
- Serum SMRP levels were significantly higher in MPM patients compared to lung cancer patients and asbestos-exposed individuals.
- Stage I MPM showed significantly higher serum SMRP than asbestos-exposed individuals (p=0.02).
- SMRP in MPM pleural effusions was significantly elevated compared to benign or non-MPM effusions (p=0.003 and p=0.044).
Conclusions:
- SMRP is a promising biomarker for MPM in both serum and pleural fluid.
- The findings support SMRP's potential role in screening asbestos-exposed cohorts.
- Further prospective studies combining SMRP with other markers are warranted.
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