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

  1. Author:
    Newton, D. L.
    Rybak, S. M.
  2. Author Address

    Rybak SM NCI, Intramural Res Support Program, SAIC Frederick, Frederick Canc Res & Dev Ctr Bldg 567,Rm 162 Frederick, MD 21702 USA NCI, Intramural Res Support Program, SAIC Frederick, Frederick Canc Res & Dev Ctr Frederick, MD 21702 USA NCI, Pharmacol & Expt Therapeut Sect, Lab Drug Discovery Res & Dev, Dev Therapeut Program,Div Canc Treatment & Diag Frederick, MD 21701 USA
    1. Year: 1998
  1. Journal: Journal of the National Cancer Institute
    1. 90
    2. 23
    3. Pages: 1787-1791
  2. Type of Article: Article
  1. 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-l cells (IC50 [50% inhibition concentration] = >100 mu g/mL), (-4)rhEDN markedly inhibited cell viability (IC50 = 6 mu g/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. [References: 27]

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  1. WOS: 000077296900011

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