Literature DB >> 8782647

Neoangiogenesis: a putative marker of malignancy in non-small-cell lung cancer (NSCLC) development.

G Fontanini1, S Vignati, D Bigini, M Lucchi, A Mussi, F Basolo, C A Angeletti, G Bevilacqua.   

Abstract

Several studies have documented a relevant prognostic role of microvessel count (MC) in non-small-cell lung carcinomas (NSCLC). However, no evidence has been reported about the involvement of neo-angiogenesis in the development of bronchial cancers. The aim of this study was to analyze microvessel density both in normal and in pathological features of the bronchial tree detected concomitantly with carcinomas. In a group of 34 patients resected for NSCLC, 48 bronchial lesions (hyperplasia, squamous metaplasia, moderate dysplasia and in situ carcinoma) were identified. In addition, 20 samples of normal bronchial epithelium from the same patients were analyzed. A monoclonal antibody was used in order to identify microvessels in the most intense areas of neovascularization from the bronchial specimens. MC was also analyzed in invasive components. An increased number of microvessels was observed from normal to dysplastic epithelium, including in situ carcinoma. Mean MC was significantly lower in normal, hyperplastic and squamous metaplastic epithelium than in dysplastic epithelium and in situ carcinoma. In particular, no differences were observed between normal and hyperplastic/metaplastic components, whereas a statistically significant difference appeared between the latter and dysplastic lesions. Moderate dysplasia and in situ carcinoma showed a number of microvessels in the lamina propria of their mucosa which were not significantly different from the invasive component, whereas hyperplastic/metaplastic lesions presented a much lower number of microvessels than invasive cancer. From these data it appears that normal bronchial epithelium and lesions associated with cancers of the bronchial tree show neovascularization in their stromal component. Hyperplasia and squamous metaplasia, unlike dysplasia and in situ carcinoma, show a low microvessel count, and they cannot represent precursor or incipient changes in the bronchial epithelium before the fully developed in situ stage has also been reached.

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Year:  1996        PMID: 8782647     DOI: 10.1002/(SICI)1097-0215(19960904)67:5<615::AID-IJC4>3.0.CO;2-X

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  8 in total

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Authors:  G Cox; W P Steward; K J O'Byrne
Journal:  Thorax       Date:  1999-02       Impact factor: 9.139

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Authors:  A J Rice; M A Steward; C M Quinn
Journal:  J Clin Pathol       Date:  2002-12       Impact factor: 3.411

Review 3.  Angiogenesis, thrombospondin, and ductal carcinoma in situ of the breast.

Authors:  A Rice; C M Quinn
Journal:  J Clin Pathol       Date:  2002-08       Impact factor: 3.411

4.  Bimodality surveillance of high-risk patients for lung cancer.

Authors:  Gordon H Downie
Journal:  Thorax       Date:  2007-04       Impact factor: 9.139

Review 5.  Angiogenesis: possibilities for therapeutic interventions.

Authors:  W Wynendaele; A T van Oosterom; A Pawinski; E A de Bruijn; R A Maes
Journal:  Pharm World Sci       Date:  1998-12

6.  Relationship between angiogenic squamous dysplasia and bronchogenic carcinoma in patients undergoing white light bronchoscopy.

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Journal:  Can Respir J       Date:  2012 May-Jun       Impact factor: 2.409

7.  Lung cancer osteopontin isoforms exhibit angiogenic functional heterogeneity.

Authors:  Justin D Blasberg; Chandra M Goparaju; Harvey I Pass; Jessica S Donington
Journal:  J Thorac Cardiovasc Surg       Date:  2009-10-09       Impact factor: 5.209

8.  Epithelial mesenchymal transition in smokers: large versus small airways and relation to airflow obstruction.

Authors:  Malik Quasir Mahmood; Sukhwinder Singh Sohal; Shakti Dhar Shukla; Chris Ward; Ashutosh Hardikar; Wan Danial Noor; Hans Konrad Muller; Darryl A Knight; Eugene Haydn Walters
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2015-08-04
  8 in total

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