Antitumor activity of interleukin-1 alpha and cisplatin in a murine model system

Arch Otolaryngol Head Neck Surg. 1995 Feb;121(2):197-200. doi: 10.1001/archotol.1995.01890020059012.

Abstract

Background: Interleukin-1 alpha (IL-1 alpha) has potent antitumor activity either alone or combined with alkylating agents such as cisplatin and mitomycin C or porfiromycin. Cisplatin is an effective chemotherapeutic agent in the treatment of advanced squamous cell carcinoma of the head and neck (SCCHN). In the murine SCCVII/SF squamous cell carcinoma tumor model, IL-1 alpha induced acute hemorrhagic necrosis and increased clonogenic cell kill.

Objective: To determine the efficacy of cisplatin and IL-1 alpha, singly and in combination, in the treatment of SCCHN.

Methods: Syngeneic C3H/HeN mice were treated with single-dose, concurrent, intraperitoneal injections of cisplatin and interleukin-1 alpha 14 days after subcutaneous tumor implantation and were monitored for delayed tumor regrowth.

Results: Cisplatin alone, but not IL-1 alpha, induced significant delayed tumor regrowth when compared with control. The combination of IL-1 alpha and cisplatin was even more effective in delaying tumor regrowth than cisplatin alone. Fractional tumor volume was significantly reduced in animals treated with the combination of cisplatin and IL-1 alpha compared with those treated with IL-1 alpha alone.

Conclusions: Results of interleukin-1 alpha and cisplatin dose-response experiments reveal that the combination of low-dose cisplatin and interleukin-1 alpha is more effective than high-dose cisplatin alone. Our data suggest that cisplatin and IL-1 alpha may be efficacious in the treatment of SCCHN.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carcinoma, Squamous Cell / pathology
  • Carcinoma, Squamous Cell / therapy*
  • Cisplatin / therapeutic use*
  • Female
  • Hemorrhage / etiology
  • Interleukin-1 / adverse effects
  • Interleukin-1 / therapeutic use*
  • Mice
  • Mice, Inbred C3H
  • Tumor Cells, Cultured

Substances

  • Interleukin-1
  • Cisplatin