TY - JOUR
T1 - Antiproliferative Activity of Human Interferons Against Ovarian Cancer Cells Grown in Human Tumor Stem Cell Assay
AU - Willson, J. K V
AU - Bittner, G.
AU - Borden, E. C.
PY - 1984/1/1
Y1 - 1984/1/1
N2 - Fresh biopsies from 14 of 22 (64%) ovarian carcinomas cultivated in the human tumor stem cell assay (HTSCA) were sensitive (>70% inhibition in cell growth) to human interferons (HuIFNs). To achieve 10 % inhibition of colony growth, 500 units/ml of a naturally produced IFN-α or IFN-αA were required in 71% of the sensitive specimens. The antiproliferative potencies of five IFNs were evaluated including two native α IFNs, two highly purified cloned subtypes of IFN-α, IFN-αD and IFN-αA, and one native fibroblast-derived beta interferon (IFN-β). The antiviral activity of the IFN-α as determined by a human cell target correlated with their relative antiproliferative action. IFN-αD had minimal inhibitory effect at the highest concentration tested, while three IFN-α with high antiviral activities were equivalent with respect to growth inhibition in the HTSCA. Although instability could not be eliminated as a contributing factor, IFN-β had significantly less growth inhibitory potency for cells from ovarian cancers when compared simultaneously with native IFN-α in the human tumor stem cell assay (HTSCA). Assuming direct antiproliferative effects are primary, future clinical trials evaluating IFN-α in ovarian cancer may require high titers of IFN.
AB - Fresh biopsies from 14 of 22 (64%) ovarian carcinomas cultivated in the human tumor stem cell assay (HTSCA) were sensitive (>70% inhibition in cell growth) to human interferons (HuIFNs). To achieve 10 % inhibition of colony growth, 500 units/ml of a naturally produced IFN-α or IFN-αA were required in 71% of the sensitive specimens. The antiproliferative potencies of five IFNs were evaluated including two native α IFNs, two highly purified cloned subtypes of IFN-α, IFN-αD and IFN-αA, and one native fibroblast-derived beta interferon (IFN-β). The antiviral activity of the IFN-α as determined by a human cell target correlated with their relative antiproliferative action. IFN-αD had minimal inhibitory effect at the highest concentration tested, while three IFN-α with high antiviral activities were equivalent with respect to growth inhibition in the HTSCA. Although instability could not be eliminated as a contributing factor, IFN-β had significantly less growth inhibitory potency for cells from ovarian cancers when compared simultaneously with native IFN-α in the human tumor stem cell assay (HTSCA). Assuming direct antiproliferative effects are primary, future clinical trials evaluating IFN-α in ovarian cancer may require high titers of IFN.
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U2 - 10.1089/jir.1984.4.441
DO - 10.1089/jir.1984.4.441
M3 - Article
C2 - 6501940
AN - SCOPUS:0021162616
SN - 0197-8357
VL - 4
SP - 441
EP - 447
JO - Journal of Interferon Research
JF - Journal of Interferon Research
IS - 4
ER -