ABUNDANCE AND STATE OF PHOSPHORYLATION OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE-PRODUCT IN HUMAN COLON CANCER

被引:39
作者
GOPE, R [1 ]
GOPE, ML [1 ]
机构
[1] CREIGHTON UNIV,CREIGHTON CANC CTR,24TH CALIFORNIA ST,CRISS 3,RM 358,OMAHA,NE 68178
关键词
RB PROTEIN; HUMAN COLORECTAL CANCERS; WESTERN AND IMMUNOBLOTS; PHOSPHORYLATION; CELL CYCLE; DNA BINDING;
D O I
10.1007/BF02454189
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In an effort to understand the possible role of Rb in cellular growth control, we have investigated the abundance and the state of phosphorylation of Rb protein (pRb) in normal and colon tumor cell lines as well as in matched colon tumors, adenomas and adjoining normal colonic mucosa. Resting normal human fibroblast cell lines were found to have only unphosphorylated pRb and phosphorylation of pRb occurred when the cells entered G1-S phase. In general, the colon tumor tissues had at least 1.5-2.0 fold increase in the abundance of pRb and 1.5-2.5 fold increase in the percentage of its phosphorylation as compared to the corresponding normal colonic mucosa. Whereas, the adenomas had similar pRb level and its phosphorylation status as observed in the normal colonic mucosa. The actively growing tumor cell lines had approximately two fold higher total pRb than normal cell lines. Although, the percentage of phosphorylated form in growing tumor cell lines as well as normal cell lines were almost equal, it was still considerably higher than normal colonic mucosa. Moreover, DNA binding assay revealed reduced binding affinity of pRb from colon tumor cell line SW480 as compared to the normal cell line WI38. These results suggest that the abundance of pRb and its phosphorylation level may have a role in the cellular growth control in human colonic epithelium.
引用
收藏
页码:123 / 133
页数:11
相关论文
共 40 条
[1]   STRUCTURE AND EXPRESSION OF THE MURINE RETINOBLASTOMA GENE AND CHARACTERIZATION OF ITS ENCODED PROTEIN [J].
BERNARDS, R ;
SCHACKLEFORD, GM ;
GERBER, MR ;
HOROWITZ, JM ;
FRIEND, SH ;
SCHARTL, M ;
BOGENMANN, E ;
RAPAPORT, JM ;
MCGEE, T ;
DRYJA, TP ;
WEINBERG, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6474-6478
[2]   INCREASED RNA-SYNTHESIS IN NUCLEAR MONOLAYERS OF WI-38 CELLS STIMULATED TO PROLIFERATE [J].
BOMBIK, BM ;
BASERGA, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (05) :2038-2042
[3]   SUPPRESSION OF TUMORIGENICITY OF HUMAN PROSTATE CARCINOMA-CELLS BY REPLACING A MUTATED RB GENE [J].
BOOKSTEIN, R ;
SHEW, JY ;
CHEN, PL ;
SCULLY, P ;
LEE, WH .
SCIENCE, 1990, 247 (4943) :712-715
[4]   THE RETINOBLASTOMA PROTEIN IS PHOSPHORYLATED DURING SPECIFIC PHASES OF THE CELL-CYCLE [J].
BUCHKOVICH, K ;
DUFFY, LA ;
HARLOW, E .
CELL, 1989, 58 (06) :1097-1105
[5]  
CAVANEE WK, 1983, NATURE, V305, P779
[6]   PHOSPHORYLATION OF THE RETINOBLASTOMA GENE-PRODUCT IS MODULATED DURING THE CELL-CYCLE AND CELLULAR-DIFFERENTIATION [J].
CHEN, PL ;
SCULLY, P ;
SHEW, JY ;
WANG, JYJ ;
LEE, WH .
CELL, 1989, 58 (06) :1193-1198
[7]   RB AND THE CELL-CYCLE - ENTRANCE OR EXIT [J].
COOPER, JA ;
WHYTE, P .
CELL, 1989, 58 (06) :1009-1011
[8]   SV40 LARGE TUMOR-ANTIGEN FORMS A SPECIFIC COMPLEX WITH THE PRODUCT OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE [J].
DECAPRIO, JA ;
LUDLOW, JW ;
FIGGE, J ;
SHEW, JY ;
HUANG, CM ;
LEE, WH ;
MARSILIO, E ;
PAUCHA, E ;
LIVINGSTON, DM .
CELL, 1988, 54 (02) :275-283
[9]   THE PRODUCT OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE HAS PROPERTIES OF A CELL-CYCLE REGULATORY ELEMENT [J].
DECAPRIO, JA ;
LUDLOW, JW ;
LYNCH, D ;
FURUKAWA, Y ;
GRIFFIN, J ;
PIWNICAWORMS, H ;
HUANG, CM ;
LIVINGSTON, DM .
CELL, 1989, 58 (06) :1085-1095
[10]   MOLECULAR-DETECTION OF DELETIONS INVOLVING BAND Q14 OF CHROMOSOME-13 IN RETINOBLASTOMAS [J].
DRYJA, TP ;
RAPAPORT, JM ;
JOYCE, JM ;
PETERSEN, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) :7391-7394