Pulmonology Medical News about non-small cell lung cancer;microvessel density;dendritic cell infiltration

Become a Member Today!
Register

Most Viewed Abstracts

1. Report Shows Shift in Starting Salaries for Physicians

2. 2008 Exclusive Survey—Earnings: Good news for primary care income

3. Medicare pay-for-reporting effort draws fire from frustrated doctors

4. Debunking Myths in the US Healthcare System

5. EGFR inhibitors as first-line therapy in advanced non-small cell lung cancer

Your Article Summary

See Latest Articles

(Click the title below to leave the MDLinx Network and go to the Journal's Website)

Tissue micro array analysis of ganglioside N-glycolyl GM3 expression and signal transducer and activator of transcription (STAT)-3 activation in relation to dendritic cell infiltration and microvessel density in non-small cell lung cancer
BMC Cancer, 06/16/09

van Cruijsen H et al. - In a study to assess the possible association of ganglioside GM3 expression and signal transducer and activator of transcription (STAT)-3 activation with suppression of dendritic cell (DC) activation and angiogenesis in non-small cell lung cancer (NSCLC), it was shown that N-glycolyl GM3 (GM3) and phosphorylated STAT3 (pSTAT3) are widely expressed in NSCLC. Based on CD83 expression, GM3, but not pSTAT3, appeared to be involved in tumor-induced DC suppression. pSTAT3 expression was not associated with microvessel density (MVD), while GM3 might play an anti-angiogenic role.

Methods

Immunohistochemistry was performed on a tissue array to determine GM3 and pSTAT3 expression in 176 primary NSCLC resections.
Median values of GM3 and pSTAT3 expression were used as cut off.
MVD was determined by CD34 staining and morphology.
CD1a and CD83 were used to determine infiltrating immature and mature dendritic cells, respectively.

Results

94% and 71% of the NSCLC samples expressed GM3 and nuclear pSTAT3, respectively.
Median overall survival was 40.0 mos.
Both low GM3 expression and high pSTAT3 expression were associated with worse survival, which reached near significance for GM3.
MVD, determined by CD34 staining and morphology, was lower in NSCLC samples with high GM3 expression.
CD1a+ cells (immature DCs) were more frequent in NSCLC tissues vs peritumoral lung tissue, while CD83+ cells (mature DCs) were more frequent in peritumoral lung tissue.
CD83+ DCs were less frequent in NSCLC tissues with high GM3 expression.

<< Previous
Streptococcus pneumoniae autolysis prevents phagocytosis and...

Next >>
Association between Cytokine Gene Polymorphisms and Risk for...