Related Experiment Video
Updated: Aug 9, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
Expression of tyrosine kinase receptors in lung carcinoids
Dan Granberg1, Erik Wilander, Kjell Oberg
1Department of Endocrine Oncology, University Hospital, Uppsala, Sweden. Dan.Granberg@medsci.uu.se
Objectives:
Typical lung carcinoids are usually relatively benign tumors, but distant metastases are seen in up to 12% of the patients. In contrast, atypical carcinoids are more aggressive tumors, displaying metastases in up to 70%. The current treatment of metastatic lung carcinoids is discouraging. New therapies, such as inhibitors of the tyrosine kinase receptor family c-kit, platelet-derived growth factor receptors (PDGFR) alpha and beta and epidermal growth factor receptor (EGFR) have shown promising results in other malignancies and might be of value in malignant lung carcinoids.
Patients And Methods:
Tumor tissue from 51 patients with typical lung carcinoids were immunostained with polyclonal antibodies against c-kit, PDGFRalpha, PDGFRbeta and EGFR. Of the 24 patients who had metastatic disease, 17 had distant metastases. Fifteen of the patients had died from their disease.
Results:
Twelve of the tumors stained positive for c-kit, 44 expressed PDGFRalpha, 30 showed positive immunoreactivity for PDGFRbeta and 26 were EGFR immunoreactive. Among the 17 patients with distant metastases, 5 tumors expressed c-kit, 12 were PDGFRalpha immunoreactive, 9 stained positive for PDGFRbeta, and 7 showed positive immunoreactivity for EGFR. There was no correlation to distant metastases or survival for c-kit, PDGFRbeta or EGFR.
Conclusions:
Tyrosine kinase receptors such as c-kit, PDGFRalpha, PDGFRbeta and EGFR are expressed in a significant number of patients with metastatic lung carcinoids. Treatment with inhibitors of the tyrosine kinase receptors expressed may be considered.
Insights
Metastatic lung carcinoids express tyrosine kinase receptors like PDGFRalpha. These receptors may be targets for new therapies, offering hope for improved treatment outcomes in aggressive lung carcinoid cases.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Lung carcinoids, particularly atypical types, can metastasize aggressively.
- Current treatments for metastatic lung carcinoids are often ineffective.
- Tyrosine kinase inhibitors show promise in other cancers.
Purpose of the Study:
- To investigate the expression of specific tyrosine kinase receptors in lung carcinoid tumors.
- To determine if these receptors are potential therapeutic targets for metastatic lung carcinoids.
Main Methods:
- Immunohistochemical staining of tumor tissue from 51 patients with typical lung carcinoids.
- Antibodies used: c-kit, platelet-derived growth factor receptors (PDGFR) alpha and beta, and epidermal growth factor receptor (EGFR).
- Analysis of receptor expression in relation to metastatic status and survival.
Main Results:
- High expression rates of PDGFRalpha (44/51), PDGFRbeta (30/51), and EGFR (26/51) were observed.
- Among patients with distant metastases, PDGFRalpha (12/17) and PDGFRbeta (9/17) were frequently expressed.
- No significant correlation was found between c-kit, PDGFRbeta, or EGFR expression and distant metastases or survival.
Conclusions:
- Tyrosine kinase receptors, especially PDGFRalpha, are expressed in a significant portion of metastatic lung carcinoid patients.
- Targeting these expressed tyrosine kinase receptors with inhibitors could be a viable therapeutic strategy.
- Further research into tyrosine kinase inhibitor efficacy for lung carcinoids is warranted.
More Related Videos
06:51Utilizing 18F-FDG PET/CT Imaging and Quantitative Histology to Measure Dynamic Changes in the Glucose Metabolism in Mouse Models of Lung Cancer
Published on: July 21, 2018
07:39The Establishment of a Lung Colonization Assay for Circulating Tumor Cell Visualization in Lung Tissues
Published on: June 16, 2018
Related Concept Videos
Receptor Tyrosine Kinases
Mitogens and the Cell Cycle