Differential display of reticulocalbin in the highly invasive cell line, MDA-MB-435, versus the poorly invasive cell line, MCF-7

被引:89
作者
Liu, ZD
Brattain, MG
Appert, H
机构
[1] MED COLL OHIO, DEPT SURG, TOLEDO, OH 43699 USA
[2] MED COLL OHIO, DEPT BIOCHEM & MOL BIOL, TOLEDO, OH 43699 USA
关键词
D O I
10.1006/bbrc.1997.6083
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
Matrigel invasion assays were used to characterize the invasive abilities of five breast cancer cell lines. Reverse Transcription Polymerase Chain Reaction (RT-PCR) was used to detect the differential gene expression of estrogen receptor (ER), E-cadherin, vimentin and cathepsin D in these cell Lines. Using mRNA differential display, we identified novel cDNA clones representing the partial sequences of genes overexpressed in the invasive MDA-MB-435 cells as compared to that of the less invasive MCF-7 cells. One of the cDNAs was homologous to reticulocalbin. The studies were repeated in all of the cell lines and the overexpression of this cDNA was confirmed by RT-PCR and Northern hybridization analysis. Reticulocalbin was expressed in the highly invasive breast cancer cell lines but was not expressed in poorly invasive ones. Although its function is still unknown, reticulocalbin is implicated in tumor cell invasiveness because of its differential expression in breast tumor cell lines. (C) 1997 Academic Press.
引用
收藏
页码:283 / 289
页数:7
相关论文
共 39 条
[1]  
ALBINI A, 1987, CANCER RES, V47, P3239
[2]   MOLECULAR AND CELLULAR ANALYSIS OF BASEMENT-MEMBRANE INVASION BY HUMAN BREAST-CANCER CELLS IN MATRIGEL-BASED INVITRO ASSAYS [J].
BAE, SN ;
ARAND, G ;
AZZAM, H ;
PAVASANT, P ;
TORRI, J ;
FRANDSEN, TL ;
THOMPSON, EW .
BREAST CANCER RESEARCH AND TREATMENT, 1993, 24 (03) :241-255
[3]  
BASSET P, 1994, CANCER-AM CANCER SOC, V74, P1045, DOI 10.1002/1097-0142(19940801)74:3+<1045::AID-CNCR2820741511>3.0.CO
[4]  
2-7
[5]  
CHOMCZYNSKI P, 1993, BIOTECHNIQUES, V15, P532
[6]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[7]  
CONOVER CA, 1994, J BIOL CHEM, V269, P7076
[8]  
Fidler I J, 1978, Adv Cancer Res, V28, P149, DOI 10.1016/S0065-230X(08)60648-X
[9]  
FRIXEN UH, 1993, CANCER RES, V53, P3618
[10]  
JOHNSON MD, 1993, CANCER RES, V53, P873