Published June 25, 2001 | Version v1
Journal article

MCM2 - a promising marker for premalignant lesions of the lung: a cohort study

  • 1. Lung Cancer Program, Roswell Park Cancer Institute, Buffalo, NY 14263 (United States)
  • 2. Department of Diabetes, Endocrinology and Metbabolism, City of Hope Medical Centre, Duarte, CA 91010 (United States)

Description

Because cells progressing to cancer must proliferate, marker proteins specific to proliferating cells may permit detection of premalignant lesions. Here we compared the sensitivities of a classic proliferation marker, Ki-67, with a new proliferation marker, MCM2, in 41 bronchial biopsy specimens representing normal mucosa, metaplasia, dysplasia, and carcinoma in situ. Parallel sections were stained with antibodies against MCM2 and Ki-67, and the frequencies of staining were independently measured by two investigators. Differences were evaluated statistically using the two-sided correlated samples t-test and Wilcoxon rank sum test. For each of the 41 specimens, the average frequency of staining by anti-MCM2 (39%) was significantly (p < 0.001) greater than by anti-Ki-67 (16%). In metaplastic lesions anti-MCM2 frequently detected cells near the epithelial surface, while anti-Ki-67 did not. We conclude that MCM2 is detectable in 2-3 times more proliferating premalignant lung cells than is Ki-67. The promise of MCM2 as a sensitive marker for premalignant lung cells is enhanced by the fact that it is present in cells at the surface of metaplastic lung lesions, which are more likely to be exfoliated into sputum. Future studies will determine if use of anti-MCM2 makes possible sufficiently early detection to significantly enhance lung cancer survival rates

Availability note (English)

Available from http://dx.doi.org/10.1186/1471-2407-1-6; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC35283

Additional details

Publishing Information

Journal Title
BMC cancer (Online)
Journal Volume
1
Journal Page Range
p. 6
ISSN
1471-2407

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46082131
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANTIBODIES; BIOPSY; CARCINOMAS; LICENSES; LUNGS; MUCOUS MEMBRANES; PROTEINS; RESPIRATORY TRACT CELLS; SURFACES
Descriptors DEC
ANIMAL CELLS; BODY; DIAGNOSTIC TECHNIQUES; DISEASES; MEMBRANES; NEOPLASMS; ORGANIC COMPOUNDS; ORGANS; RESPIRATORY SYSTEM; SOMATIC CELLS

Optional Information

Copyright
Copyright (c) 2001 Tan et al
Notes
PMCID: PMC35283; PUBLISHER-ID: 1471-2407-1-6; PMID: 11472637; OAI: oai:pubmedcentral.nih.gov:35283; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.