Important note: Information in this article was accurate in 1995. The state of the art may have changed since the publication date.
HIV cross-reactive antigens in breast and gynecological cancer (Meeting abstract).
Proc Annu Meet Am Assoc Cancer Res; 35:A2975 1994. Unique Identifier : AIDSLINE ICDB/95604660 Rakowicz-Szulczynska EM; McIntosh DG; Piao J; Smith M; Dept. of Obstetrics and Gynecology, Univ. of Nebraska Medical; Center, 600 South 42nd St., Omaha, NE 68198-3255
Abstract:
We have identified a novel family of breast cancer- and gynecological cancer-associated antigens which cross-react in western blotting and are immunoprecipitated with a monoclonal antibody (MAb) developed against the variable loop of the human immunodeficiency virus (HIV-I) envelope protein gp120. Four HIV cross-reactive antigens are detected in breast cancer (p160/p80, p45 and p24) and three antigens (p120, p41, and p24) in gynecological cancer (ovarian, cervical, endometrial, vulvar), the molecular weights of which correspond to known HIV antigens. All cancer antigens exhibit plasma membrane/cytoplasmic localization, and p24 is also expressed in the chromatin. Antibodies produced by HIV-infected patients detect cancer antigens p80, p45/p41, and p24. HIV cross-reactive antigens, with the exception of p24, are neither detectable on normal epithelial cells nor in cancer of the gastrointestinal tract, lung cancer, and melanoma. We suggest that the novel antigens represent either the product(s) of an unknown retrovirus of homology to HIV, or the products of a cellular proto-oncogene(s). Antigen p160- and p120-mediated internalization of MAb leads to a growth-modulatory effect. 125I-labeled MAb exerts a cytotoxic effect due to the chromosomal damage caused by the radiation of 125I-MAb that becomes chromatin bound, and may represent a useful tool in cancer immunotherapy.
Keywords: Breast Neoplasms/*IMMUNOLOGY Female Genital Neoplasms, Female/*IMMUNOLOGY Human HIV Antigens/*ANALYSIS ABSTRACT 950330
M9530835
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