Antitumor activity of cytotropic heterogeneous molecular lipids (CHML) on human breast cancer xenograft in nude mice

Citation
Qm. Zhan et al., Antitumor activity of cytotropic heterogeneous molecular lipids (CHML) on human breast cancer xenograft in nude mice, ANTICANC R, 21(4A), 2001, pp. 2477-2482
Citations number
21
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
21
Issue
4A
Year of publication
2001
Pages
2477 - 2482
Database
ISI
SICI code
0250-7005(200107/08)21:4A<2477:AAOCHM>2.0.ZU;2-N
Abstract
Cytotropic heterogeneous molecular lipid (CHML), which is a new anticancer agent with US patent number 5,260,067, has recently been shown to suppress tumor cell growth in multiple tumor lines and induce apoptosis in vitro (1) . These results indicate that CHML may be an effective antitumor agent. In the present study, using both local injection and intravenous injection, we have investigated the suppressive effect of CHML on human breast caner cel ls MCF-7 xenograft in nude mice. In the local injection, CHML was introduce d into nude mice implanted with human breast cancer xenograft at doses of 2 5 mg/tumor area (cm(2)), 35 mg/tumor area (cm(2)), or 50 mg/tumor area (cm( 2)), once every two days, total 3 times. The inhibition of tumor growth was 81.3%, 93.8% and 100%, respectively. In the intravenous injection, the nud e mice bearing MCF-7 xenografts were treated with CHML at 10 mg/kg/day, or 15 mg/kg/day, or 20 mg/kg/day, once a day, total 7 days, the growth inhibit ion of tumor area was 58.1%, 77.4%, and 83.9%, respectively. At the same ti me, the toxicity of CHML was determined through examining the number of the white blood cell (WBC) and the activity of the serum glutamic-pyruvic tran saminase (SGPT). However, no evident alterations of WBC and SGPT were detec ted in all animals treated with CHML, suggesting that CHML has little toxic ity on nude mice. Taken together, these results indicate that CHML is an ef fective agent that suppresses breast tumor growth and suggest the possibili ty of using CHML in the clinical trial in the near future.