Low COX2 in tumor and upregulation in stroma mark laryngeal squamous cell carcinoma progression
✍ Scribed by Konstantinos Kourelis; Gerasimos Vandoros; Theodoros Kourelis; Theodoros Papadas; Panos Goumas; Georgia Sotiropoulou-Bonikou
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 271 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0023-852X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Objectives/Hypothesis:
Invasive squamous cell carcinomas (SCC) of the larynx, like most solid tumors, are surrounded by a reactive stroma, in which cancer associated fibroblasts (CAFs) are the predominant cell type. This mesenchymal reaction may affect cancer progression multiply. The proinflammatory enzyme cyclooxygenase‐2 (COX‐2) has been correlated with head and neck cancer. This study aims to explore the impact of epithelial and stromal COX‐2 expression on SCC behavior.
Study Design:
Retrospective case review study performed in a tertiary health center institution.
Methods:
Double immunohistochemistry of COX‐2 and the CAF marker α‐smooth muscle actin (α‐SMA) was utilized in 97 laryngeal cancer patients. Follow‐up data were collected in 52 cases.
Results:
Low COX‐2 immunostaining in cancer cells was associated with advanced grade (P = .044) and shorter recurrence‐free period (P = .035). CAF expression was positively correlated with the grade of the infiltrating tumor (P = .030).
Conclusions:
In laryngeal SCCs, COX‐2 may exert its deleterious effect by alterations in the tumor microenvironment. CAF‐derived, COX‐2‐mediated paracrine influences on malignant cells possibly facilitate cancer progression. Overlooking the stromal remodeling could account for unsuccessful treatments of epithelial neoplasms. Laryngoscope, 2009
📜 SIMILAR VOLUMES
## Background: Angiogenesis is essential for solid tumor growth and metastasis. vascular endothelial growth factor (vegf), a recently identified growth factor with significant angiogenic properties, may be a major tumor angiogenesis regulator in vivo. conversely, there have been few studies of the
## Abstract The aim of our study was to analyze the alterations of some candidate tumor suppressor genes (TSGs) viz. __LIMD1__, __LTF__, __CDC25A__, __SCOTIN__, __RASSF1A__ and __CACNA2D2__ located in the chromosomal region 3p21.31 associated with the development of early dysplastic lesions of head