Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1985 Feb;40(2):85-90.
doi: 10.1136/thx.40.2.85.

Neurone specific enolase: a useful diagnostic serum marker for small cell carcinoma of the lung

Neurone specific enolase: a useful diagnostic serum marker for small cell carcinoma of the lung

T Esscher et al. Thorax. 1985 Feb.

Abstract

Among lung cancers small cell carcinoma is the most sensitive to chemotherapy and radiation. This has emphasised the importance of an accurate diagnosis of this cell type, and the present study examined the use of serum neurone specific enolase (NSE) as a diagnostic marker for small cell carcinoma. NSE was measured in pretreatment sera from 103 patients with small cell carcinoma and in sera from relevant controls, including patients with other lung cancers, non-malignant lung diseases, and healthy adults. Serum NSE concentration was raised (greater than 25 ng/ml) in 72% of patients with small cell carcinoma. Ninety one per cent of patients with extensive disease and 50% of patients with limited disease were serum NSE positive. Patients with extensive disease in general had higher serum NSE concentrations than patients with limited disease. No definite difference in serum NSE positivity could be shown between oat cell and intermediate cell subtypes. Out of 51 patients with other lung cancers, four (8%) had a raised serum concentration, whereas all patients with non-malignant diseases and healthy individuals had normal serum NSE concentrations. Serum NSE determination seems to be a valuable tool for the diagnosis of small cell carcinoma.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biochem Biophys Res Commun. 1975 Sep 16;66(2):814-20 - PubMed
    1. Biochim Biophys Acta. 1976 Nov 8;452(1):245-52 - PubMed
    1. J Neurochem. 1977 May;28(5):1097-107 - PubMed
    1. Brain Res. 1978 Jul 7;150(1):117-33 - PubMed
    1. Ann Surg. 1981 May;193(5):539-48 - PubMed

Publication types

Substances