FLOW CYTOMETRIC ANALYSIS OF DNA CONTENT AND KERATINS BY USING CK7, CK8, CK18, CK19, AND KL1 MONOCLONAL-ANTIBODIES IN BENIGN AND MALIGNANT HUMAN BREAST-TUMORS

被引:47
作者
FERRERO, M
SPYRATOS, F
LEDOUSSAL, V
DESPLACES, A
ROUESSE, J
机构
[1] CTR RENE HUGUENIN LUTTE CONTRE LE CANC, DEPT BIOL, 35 RUE DAILLY, F-92211 ST CLOUD, FRANCE
[2] CTR RENE HUGUENIN LUTTE CONTRE LE CANC, DEPT ANAT PATHOL, F-92211 ST CLOUD, FRANCE
[3] CTR RENE HUGUENIN LUTTE CONTRE LE CANC, DEPT MED, F-92211 ST CLOUD, FRANCE
来源
CYTOMETRY | 1990年 / 11卷 / 06期
关键词
breast cancer; DNA analysis; Flow cytometry;
D O I
10.1002/cyto.990110609
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have used a double‐labelling flow cytometry analysis of keratin (CK) and DNA in breast cancer. Five monoclonal anti‐keratin antibodies were tested: KL1 recognizing Mr 55,000–57,000 keratins, and “anti‐glandular epithelia,” LE41, RGE‐53, and LP2K specific for CK n° 7, 8, 18, and 19 of Moll's classification, respectively. Flow cytometric (DNA‐CK) analysis was performed on 10 benign and 19 malignant human breast tumors. All the benign tumors were diploid and 63% of the malignant tumors were aneuploid. This technique permits the analysis of DNA in the epithelial fraction alone. In aneuploid tumors, gating the DNA‐keratin‐positive population allowed accurate DNA analysis without interference due to debris background and non‐epithelial cells. Moreover, double‐labelling using the CK19 antibody gave a better identification of near‐diploid tumors. An enhancement of keratin expression in malignant tumors was observed with CK 19 (P < 0.001), KL1 (P < 0.01), CK 8 (P < 0.05), and CK18 (n.s.) compared to benign tumors. The comparison of keratin expression in aneuploid and diploid malignant tumors revealed reduced CK8, CK18, and CK19 in the former. Copyright © 1990 Wiley‐Liss, Inc.
引用
收藏
页码:716 / 724
页数:9
相关论文
共 38 条
  • [31] COMPARISON OF CYTOKERATIN EXPRESSION IN PRIMARY AND METASTATIC CARCINOMAS - DIAGNOSTIC APPLICATION IN SURGICAL PATHOLOGY
    SHAH, KD
    TABIBZADEH, SS
    GERBER, MA
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1987, 87 (06) : 708 - 715
  • [32] TISSUE-SPECIFIC MARKERS IN FLOW-CYTOMETRY OF UROLOGICAL CANCERS .3. COMPARING CHROMOSOMAL AND FLOW CYTOMETRIC DNA ANALYSIS OF BLADDER-TUMORS
    SMEETS, AWGB
    PAUWELS, RPE
    BECK, JLM
    GERAEDTS, JPM
    DEBRUYNE, FMJ
    LAARAKKERS, L
    FEITZ, WFJ
    VOOIJS, GP
    RAMAEKERS, FCS
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (03) : 304 - 310
  • [33] SPYRATOS F, 1987, ANAL QUANT CYTOL, V9, P485
  • [34] PROGNOSTIC VALUE OF ESTROGEN AND PROGESTERONE RECEPTORS IN PRIMARY INFILTRATING DUCTAL BREAST-CANCER - A SEQUENTIAL MULTIVARIATE-ANALYSIS OF 1262 PATIENTS
    SPYRATOS, F
    HACENE, K
    TUBIANAHULIN, M
    PALLUD, C
    BRUNET, M
    [J]. EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1989, 25 (08): : 1233 - 1240
  • [35] KERATIN-19 - PREDICTED AMINO-ACID SEQUENCE AND BROAD TISSUE DISTRIBUTION SUGGEST IT EVOLVED FROM KERATINOCYTE KERATINS
    STASIAK, PC
    PURKIS, PE
    LEIGH, IM
    LANE, EB
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 92 (05) : 707 - 716
  • [36] TOLLE HG, 1985, EUR J CELL BIOL, V38, P234
  • [37] REACTIVITY PATTERN OF A MONOCLONAL ANTIKERATIN ANTIBODY (KL1)
    VIAC, J
    REANO, A
    BROCHIER, J
    STAQUET, MJ
    THIVOLET, J
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (04) : 351 - 354
  • [38] KERATIN POLYPEPTIDE COMPOSITION AS A BIOCHEMICAL TOOL FOR THE DISCRIMINATION OF BENIGN AND MALIGNANT EPITHELIAL LESIONS IN MAN
    WINTER, H
    SCHWEIZER, J
    GOERTTLER, K
    [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1983, 275 (01) : 27 - 34