LEWIS BLOOD-GROUP ANTIGEN-A AND ANTIGEN-B IN HUMAN BREAST TISSUES - LOSS OF LEWIS-B IN BREAST-CANCER CELLS AND CORRELATION WITH TUMOR GRADE

被引:1
作者
IDIKIO, HA
MANICKAVEL, V
机构
[1] Department of Pathology, University of Alberta, Edmonton, Alberta
关键词
D O I
10.1002/1097-0142(19910915)68:6<1303::AID-CNCR2820680620>3.0.CO;2-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Lewis blood group antigens (Lewis-a [Le(a)] and Lewis-b [Le(b)]) and their precursors are present on various normal human epithelial cell surfaces. The authors examined 35 benign and malignant human breast lesions using mouse monoclonal antibodies to synthetic Le(a) and Le(b) carbohydrate antigens. Normal breast lobular and ductal epithelium and benign breast lesions showed Le(b) staining but only occasional Le(a) staining. In invasive ductal carcinomas of breast, of all grades, a loss of Le(b) antigen staining was found in 80% of the breast cancer cases. This reduced Le(b) antigen expression increased with the grade of malignancy. Therefore, the loss of Le(b) blood group antigens on breast cancer cell surfaces may suggest altered fucosylation patterns in malignant cells and reflect the degree of malignancy and/or invasiveness.
引用
收藏
页码:1303 / 1308
页数:6
相关论文
共 48 条
[31]   SUBCELLULAR-LOCALIZATION OF BLOOD-GROUP LE(B) CARBOHYDRATE ANTIGEN (MSN-1-REACTIVE ANTIGEN) IN ENDOMETRIAL CANCER-CELLS [J].
SUSUMU, N ;
KAWAKAMI, H ;
AOKI, D ;
HIRANO, H ;
NOZAWA, S .
CANCER RESEARCH, 1993, 53 (15) :3643-3648
[32]   A AND B BLOOD-GROUP ANTIGEN EXPRESSION ON MIXED COLONY CELLS AND ERYTHROID PRECURSORS - RELEVANCE FOR HUMAN ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
BLACKLOCK, HA ;
KATZ, F ;
MICHALEVICZ, R ;
HAZLEHURST, GRP ;
DAVIES, L ;
PRENTICE, HG ;
HOFFBRAND, AV .
BRITISH JOURNAL OF HAEMATOLOGY, 1984, 58 (02) :267-276
[33]   Novel ganglioside antigen identified by B cells in human medullary breast carcinomas: The proof of principle concerning the tumor-infiltrating B lymphocytes [J].
Kotlan, B ;
Simsa, P ;
Teillaud, JL ;
Fridman, WH ;
Toth, J ;
McKnight, M ;
Glassy, MC .
JOURNAL OF IMMUNOLOGY, 2005, 175 (04) :2278-2285
[34]   Antigen Specificity and Clinical Significance of IgG and IgA Autoantibodies Produced in situ by Tumor-Infiltrating B Cells in Breast Cancer [J].
Garaud, Soizic ;
Zayakin, Pawel ;
Buisseret, Laurence ;
Rulle, Undine ;
Silina, Karina ;
de Wind, Alexandre ;
Van den Eyden, Gert ;
Larsimont, Denis ;
Willard-Gallo, Karen ;
Line, Aija .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[35]   Translocation of an intracellular antigen to the surface of medullary breast cancer cells early in apoptosis allows for an antigen-driven antibody response elicited by tumor-infiltrating B cells [J].
Hansen, MH ;
Nielsen, HV ;
Ditzel, HJ .
JOURNAL OF IMMUNOLOGY, 2002, 169 (05) :2701-2711
[36]   EXPRESSION OF BLOOD-GROUP-RELATED ANTIGENS, ABH, LEWIS A, B, X AND Y, AND CA 19-9 IN PANCREATIC-CANCER CELLS IN COMPARISON WITH THE PATIENTS BLOOD-GROUP TYPE [J].
POUR, PM ;
TEMPERO, MA ;
TAKASAKI, H ;
UCHIDA, E ;
TAKIYAMA, Y ;
BURNETT, DA ;
STEPLEWSKI, Z .
DIGESTION, 1988, 40 (02) :109-109
[37]   EXPRESSION OF TUMOR-ASSOCIATED 90K-ANTIGEN IN HUMAN BREAST-CANCER - NO CORRELATION WITH PROGNOSIS AND RESPONSE TO FIRST-LINE THERAPY WITH TAMOXIFEN [J].
FOEKENS, JA ;
KLIJN, JGM ;
NATOLI, C ;
VANPUTTEN, WLJ ;
DISTEFANO, P ;
LOOK, MP ;
PORTENGEN, H ;
IACOBELLI, S .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (02) :130-134
[38]   Study of the expression of Tn antigen in different types of human breast cancer cells using VVA-B4 lectin [J].
Konska, G ;
Guerry, M ;
Caldefie-Chezet, F ;
De Latour, M ;
Guillot, J .
ONCOLOGY REPORTS, 2006, 15 (02) :305-310
[39]   MOLECULAR RECOGNITION .7. SYNTHETIC, CONFORMATIONAL, AND IMMUNOCHEMICAL STUDIES OF MODIFIED LEWIS-B AND Y-HUMAN BLOOD-GROUP DETERMINANTS TO SERVE AS PROBES FOR THE COMBINING SITE OF THE LECTIN-IV OF GRIFFONIA-SIMPLICIFOLIA [J].
SPOHR, U ;
LEMIEUX, RU .
CARBOHYDRATE RESEARCH, 1988, 174 :211-237
[40]   Histo-blood group A/B antigen deletion/reduction vs. continuous expression in human tumor cells as correlated with their malignancy [J].
Ichikawa, D ;
Handa, K ;
Hakomori, S .
INTERNATIONAL JOURNAL OF CANCER, 1998, 76 (02) :284-289