Growth inhibition of human ovarian cancers by cytotoxic analogues of luteinizing hormone-releasing hormone

J Natl Cancer Inst. 1997 Dec 3;89(23):1803-9. doi: 10.1093/jnci/89.23.1803.

Abstract

Background: Receptors for luteinizing hormone-releasing hormone (LH-RH) are found in nearly 80% of human ovarian cancers. The chemotherapeutic agent doxorubicin can be linked to [D-lysine6]LH-RH to form a cytotoxic analogue (AN-152) that may have greater specificity for tumor cells. This study was conducted to investigate the effects of AN-152 on the growth of LH-RH receptor-positive OV-1063 human epithelial ovarian cancers.

Methods: Nude mice bearing human ovarian tumors, OV-1063 or UCI-107 (LH-RH receptor negative), were injected intraperitoneally with saline (control) or with equimolar doses of AN-152 or doxorubicin; experiments involving mice with OV-1063 tumors also included groups that were administered [D-lysine6]LH-RH either alone or in combination with doxorubicin. Tumor volume, weight, doubling time, and burden (i.e., tumor weight/body weight) as well as tumor apoptotic and mitotic indices were determined. The levels of receptors for LH-RH and epidermal growth factor (EGF) and their messenger RNAs were measured by use of radioreceptor and reverse transcription-polymerase chain reaction assays, respectively.

Results: The growth of OV-1063 ovarian tumors in nude mice, as based on reduction in tumor volume, was inhibited significantly (all P<.05, two-sided) 4 weeks after treatment with AN-152, even at the lowest dose tested (413 nmol/20 g weight); the toxic effects of an equivalent dose of doxorubicin caused substantial mortality. High-affinity receptors for LH-RH and EGF were found on cell membranes of OV-1063 cancers; however, after in vivo treatment with AN-152, LH-RH receptor-binding sites were not detectable and EGF receptors were reduced in number. The growth of UCI-107 ovarian cancers was not inhibited by AN-152.

Conclusions: In nude mice bearing LH-RH receptor positive OV-1063 epithelial ovarian cancers, systemic administration of AN-152 is less toxic and inhibits tumor growth better than equimolar doses of doxorubicin.

Publication types

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

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / therapeutic use*
  • Apoptosis / drug effects
  • Blotting, Southern
  • Carcinoma / drug therapy*
  • Carcinoma / metabolism
  • Doxorubicin / analogs & derivatives*
  • Doxorubicin / therapeutic use*
  • Epidermal Growth Factor / blood
  • Epidermal Growth Factor / genetics
  • ErbB Receptors / genetics
  • Female
  • Gonadotropin-Releasing Hormone / analogs & derivatives*
  • Gonadotropin-Releasing Hormone / therapeutic use*
  • Humans
  • Luteinizing Hormone / blood
  • Luteinizing Hormone / genetics
  • Mice
  • Mice, Nude
  • Mitotic Index / drug effects
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / metabolism
  • Polymerase Chain Reaction / methods
  • RNA, Messenger / analysis
  • RNA, Neoplasm / analysis
  • Receptors, LHRH / drug effects*
  • Receptors, LHRH / metabolism
  • Transcription, Genetic
  • Tumor Cells, Cultured

Substances

  • Antibiotics, Antineoplastic
  • RNA, Messenger
  • RNA, Neoplasm
  • Receptors, LHRH
  • LHRH, lysine(6)-doxorubicin
  • Gonadotropin-Releasing Hormone
  • Epidermal Growth Factor
  • Doxorubicin
  • Luteinizing Hormone
  • ErbB Receptors