Serum levels of tumor necrosis factor in squamous cell carcinoma of the head and neck

1994 ◽  
Vol 15 (4) ◽  
pp. 281-285 ◽  
Author(s):  
Levent Soylu ◽  
Cengiz Özcan ◽  
Fikret Çetik ◽  
Semra Paydaş ◽  
Mete Kiroǧlu ◽  
...  
1992 ◽  
Vol 102 (4) ◽  
pp. 447-450 ◽  
Author(s):  
Oreste Gallo ◽  
Stefania Pinto ◽  
Simone Boccuzzi ◽  
Maurizio Dilaghi ◽  
Ezio Gallina ◽  
...  

1995 ◽  
Vol 104 (3) ◽  
pp. 203-209 ◽  
Author(s):  
Eric A. Mann ◽  
Margaret S. Hibbs ◽  
Xtn Ze Wang ◽  
Jeffrey D. Spiro ◽  
Michael Clawson ◽  
...  

Gelatinases (GLs) belong to a family of enzymes known as matrix metalloproteinases (MMPs), which are produced by both normal and neoplastic cells. These enzymes have been implicated in tumor invasion and metastasis, although the mechanism of regulation of tumor MMP production is unknown. Since our previous studies have shown that numerous cytokines are present in the tumor microenvironment, our goal was to establish the effect of selected cytokines on GL production by both established tumor cell lines and primary cultures of head and neck squamous cell carcinoma (HNSCC). Supernatants of HNSCC cell lines SCC-25 and FADU stimulated with interleukin (IL)-1α and IL-1β demonstrated modest induction of 92 kd GL production by zymogram analysis when compared with controls; IL-2, IL-6, and interferon-γ had no consistent effect on MMP production. Stimulation of cell lines with tumor necrosis factor (TNF)-α (104 to 10 U/mL), however, dramatically enhanced production of 92 kd GL by both cell lines in a dose-dependent fashion, although tissue inhibitor of metalloproteinase (TIMP) expression was unaffected. Northern blot analysis showed that this enhancement of 92 kd GL occurred at the messenger RNA level. Stimulation of short-term primary tumor cultures with TNF-α resulted in significant enhancement of 92 kd GL expression in one of four cultures and enhancement of 72 kd GL expression in all cultures. The observed increase in GL expression by TNF-α suggests a role for this cytokine in the regulation of GL expression by tumor cells during invasion and metastasis.


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