[The effect of IRESSA on H22 mouse hepatocellular carcinoma]

Zhonghua Yi Xue Za Zhi. 2004 Apr 17;84(8):684-6.
[Article in Chinese]

Abstract

Objective: To investigate the effect of IRESSA (gefitinib, ZD1839) on H22 murine hepatocellular carcinoma.

Methods: Mice bearing H22 hepatocellular carcinoma were randomly divided into oral control group, Normal saline (NS) control group, cisplatin (CDDP) d1-5 group, CDDP d6-10 group, IRESSA group, IRESSA combined with CDDP early (IRESSA + CDDP d1-5) group, and IRESSA combined with CDDP lately (IRESSA + CDDP d6-10) group. IRESSA was given by daily gastrogavage for 10 days (day 1-day 10) at 100 mg/kg in body weight (BW). CDDP was given by daily intraperitoneal injection for 5 days (day 1-day 5, or day 6-day 10) at 1.2 mg/kg in BW. The growth inhibiting rate (IR) of tumor, change of BW, spleen index (SI), and amounts of blood leucocyte or hemoglobin were detected.

Results: IR of tumor in IRESSA group was not significantly difference with that in CDDP d1-5 group, CDDP d6-10 group, IRESSA + CDDP d1-5 group (P > 0.05). IR of tumor in IRESSA group, CDDP d1-5 group, CDDP d6-10 group, IRESSA and IRESSA + CDDP d1-5 group were 41%, 54%, 46%, and 56%, respectively. IR of tumor in IRESSA + CDDP d6-10 group (26%) was significantly lower than that in CDDP d6-10 group (P < 0.05) or in IRESSA + CDDP d1-5 group (P < 0.01). Compared with oral or NS control groups, SI and net BW in IRESSA group was not significantly difference (P > 0.05). SI and net BW in both IRESSA + CDDP d1-5 group and IRESSA + CDDP d6-10 group were lower markedly than those in IRESSA group (P < 0.01).

Conclusion: Tumor growth of H22 bearing mice was markedly inhibited by IRESSA.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Carcinoma, Hepatocellular / drug therapy*
  • Cisplatin / therapeutic use
  • Disease Models, Animal
  • Gefitinib
  • Liver Neoplasms / drug therapy*
  • Mice
  • Quinazolines / therapeutic use*
  • Random Allocation
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Quinazolines
  • Cisplatin
  • Gefitinib