CORRELATION OF P-GLYCOPROTEIN DETECTION BY IMMUNOHISTOCHEMISTRY WITH MDR-1 MESSENGER-RNA LEVELS IN OSTEOSARCOMAS - PILOT-STUDY

被引:18
作者
KANDEL, RA
CAMPBELL, S
NOBLETOPHAM, S
BELL, R
ANDRULIS, IL
机构
[1] UNIV TORONTO,MT SINAI HOSP,DEPT ORTHOPED SURG,TORONTO,ON M5G 1X5,CANADA
[2] UNIV TORONTO,MT SINAI HOSP,SAMUEL LUNENFELD RES INST,TORONTO,ON M5G 1X5,CANADA
关键词
OSTEOSARCOMA; MULTIDRUG RESISTANCE; P-GLYCOPROTEIN; IMMUNOHISTOCHEMISTRY; RT-PCR;
D O I
10.1097/00019606-199503000-00011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All the factors that influence prognosis in patients with osteosarcomas have not been fully determined. One reported predictor of poor outcome is increased multi-drug resistant gene (mdr-1) expression, as measured by reverse transcription and polymerase chain reaction (RTPCR). We examined whether immunostaining for p-glycoprotein, the protein product of mdr-1, could be used instead of RT-PCR to indicate the presence of the multidrug-resistant phenotype. The sensitivity of the immunostaining was determined using KB cell sublines. For 13 cases of osteosarcoma, samples were immunostained for p-glycoprotein and the levels of mdr-1 expression quantitated with use of RT-PCR. Three osteosarcomas with undetectable levels of mdr-1 expression by RT-PCR were negative immunohistochemically. Ten cases showed mdr-1 expression ranging from approximately 1 to 32 copies of mdr-1 mRNA/cell. Of these cases, five cases contained occasional tumour cells with positive immunostaining. There was no correlation between levels of expression and the presence or number of immunoreactive cells. These results indicate that the presence of p-glycoprotein immunostaining does not reliably correlate with the level of mdr-1 expression. However it may be useful in conjunction with RT-PCR to further define different subgroups of osteosarcomas that may have different prognoses, and this is currently under investigation.
引用
收藏
页码:59 / 65
页数:7
相关论文
共 42 条
[1]   ISOLATION AND GENETIC-CHARACTERIZATION OF HUMAN KB-CELL LINES RESISTANT TO MULTIPLE-DRUGS [J].
AKIYAMA, SI ;
FOJO, A ;
HANOVER, JA ;
PASTAN, I ;
GOTTESMAN, MM .
SOMATIC CELL AND MOLECULAR GENETICS, 1985, 11 (02) :117-126
[2]  
ARCECI RJ, 1993, BLOOD, V81, P2215
[3]  
BATES SE, 1991, AM J PATHOL, V139, P305
[4]   IMMUNOHISTOCHEMICAL DETECTION OF P-GLYCOPROTEIN IN NORMAL AND MALIGNANT-TISSUES - A COMPARATIVE-STUDY OF 3 MONOCLONAL-ANTIBODIES, JS']JSB-L, C219 AND 265/F4, AGAINST DIFFERENT EPITOPES USING FROZEN AND PARAFFIN TISSUE-SECTIONS [J].
BITTL, A ;
NAP, M ;
JAGER, W ;
LATHAN, B ;
LANG, N .
TUMOR BIOLOGY, 1993, 14 (03) :155-166
[5]  
CHAN HSL, 1988, LAB INVEST, V59, P870
[6]   IMMUNOHISTOCHEMICAL DETECTION OF P-GLYCOPROTEIN - PROGNOSTIC CORRELATION IN SOFT-TISSUE SARCOMA OF CHILDHOOD [J].
CHAN, HSL ;
THORNER, PS ;
HADDAD, G ;
LING, V .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (04) :689-704
[7]   MULTIDRUG RESISTANCE AFTER RETROVIRAL TRANSFER OF THE HUMAN MDR1 GENE CORRELATES WITH P-GLYCOPROTEIN DENSITY IN THE PLASMA-MEMBRANE AND IS NOT AFFECTED BY CYTOTOXIC SELECTION [J].
CHOI, K ;
FROMMEL, TO ;
STERN, RK ;
PEREZ, CF ;
KRIEGLER, M ;
TSURUO, T ;
RONINSON, IB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7386-7390
[8]  
CLYNES M, 1993, IN VITRO CELL DEV-AN, V29A, P171
[9]  
DALTON WS, 1989, BLOOD, V73, P747
[10]  
EPSTEIN J, 1989, BLOOD, V74, P913