Unique recombinant human ribonuclease and inhibition of Kaposi's sarcoma cell growth

J Natl Cancer Inst. 1998 Dec 2;90(23):1787-91. doi: 10.1093/jnci/90.23.1787.

Abstract

Background: Preparations of human chorionic gonadotropin (hCG) have been shown to exhibit anti-Kaposi's sarcoma (KS) activity, but the identity of the responsible agent(s) remains controversial. One candidate agent is an eosinophil-derived neurotoxin (EDN)-like polypeptide that contaminates preparations of hCG. We have genetically engineered a unique form of hEDN, which is a ribonuclease, and have evaluated the cytotoxic effects of the recombinant protein on KS Y-1 cells and on cells of other cancer types.

Methods: The amino-terminus of hEDN was extended by four amino acid residues, corresponding to the proximal part of the hEDN signal peptide (serine, leucine, histidine, and valine; positions -4 to -1, respectively), by use of the polymerase chain reaction and an hEDN complementary DNA. The recombinant protein was isolated from bacterial inclusion bodies. The cytotoxic activity of this hEDN variant, (-4)rhEDN, was tested on KS Y-1 cells and human glioma, melanoma, breast carcinoma, and renal carcinoma cells.

Results: Approximately half of the anti-KS activity in a crude commercial preparation of hCG was associated with a polypeptide that reacted with anti-recombinant-hEDN (rhEDN) polyclonal antibodies. Although rhEDN protein displayed little cytotoxicity against KS Y-1 cells (IC50 [50% inhibition concentration] = >100 microg/mL), (-4)rhEDN markedly inhibited cell viability (IC50 = 6 microg/mL). Neither version of rhEDN inhibited the viability of other tested human cancer cell types.

Conclusions: A four amino acid extension of the amino-terminus of rhEDN confers cytotoxicity against KS Y-1 cells in vitro. Design of the (-4)rhEDN variant was based on the sequence of a natural human protein associated with hCG. Our results suggest that (-4)rhEDN is one of the agents in hCG responsible for anti-KS activity. A purified molecule is thus available for in vitro and in vivo mechanistic and, possibly, future clinical studies.

Publication types

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

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Blotting, Western
  • Breast Neoplasms / drug therapy
  • DNA, Complementary / chemical synthesis
  • Eosinophil-Derived Neurotoxin
  • Genes, Synthetic
  • Histidine / genetics
  • Humans
  • Kidney Neoplasms / drug therapy
  • Leucine / genetics
  • Polymerase Chain Reaction / methods
  • Proteins / therapeutic use*
  • Recombinant Proteins / therapeutic use
  • Ribonuclease, Pancreatic / therapeutic use*
  • Ribonucleases*
  • Sarcoma, Kaposi / drug therapy*
  • Sarcoma, Kaposi / metabolism
  • Serine / genetics
  • Tumor Cells, Cultured / drug effects
  • Valine / genetics

Substances

  • Antineoplastic Agents
  • DNA, Complementary
  • Proteins
  • Recombinant Proteins
  • Serine
  • Histidine
  • Eosinophil-Derived Neurotoxin
  • Ribonucleases
  • Ribonuclease, Pancreatic
  • Leucine
  • Valine