INDUCING DIFFERENTIATION OF TRANSFORMED-CELLS WITH HYBRID POLAR COMPOUNDS - A CELL CYCLE-DEPENDENT PROCESS

被引:95
作者
MARKS, PA
RICHON, VM
KIYOKAWA, H
RIFKIND, RA
机构
[1] Program of Cell Biology and Genetics, DeWitt Wallace Research Laboratory, Mem. Sloan-Kettering Cancer Center, New York
关键词
D O I
10.1073/pnas.91.22.10251
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transformed cells do not necessarily lose their capacity to differentiate. Various agents can induce many types of neoplastic cells to terminal differentiation. Among such inducers, a particularly potent group consists of hybrid polar compounds; hexamethylene bisacetamide (HMBA) is the prototype of this group. With virus-transformed murine erythroleukemia cells as a model, HMBA was shown to cause these cells to arrest in G(1) phase and express globin genes. This review focuses on HMBA-induced modulation of factors regulating G(1)-to-S phase progression, including a decrease in the G(1) cyclin-dependent kinase cdk4, associated with inhibition of phosphorylation of the retinoblastoma protein pRB and possibly other related proteins that, in turn, sequester factors required for initiation of DNA synthesis; this provides a possible mechanism for HMBA-induced terminal cell division. Evidence that hybrid polar compounds have therapeutic potential for cancer treatment will also be reviewed.
引用
收藏
页码:10251 / 10254
页数:4
相关论文
共 48 条
[31]   COLONY-STIMULATING FACTOR-I REGULATES NOVEL CYCLINS DURING THE G1 PHASE OF THE CELL-CYCLE [J].
MATSUSHIME, H ;
ROUSSEL, MF ;
ASHMUN, RA ;
SHERR, CJ .
CELL, 1991, 65 (04) :701-713
[32]   PROTEIN-KINASE-C ACTIVITY AND HEXAMETHYLENEBISACETAMIDE-INDUCED ERYTHROLEUKEMIA CELL-DIFFERENTIATION [J].
MELLONI, E ;
PONTREMOLI, S ;
MICHETTI, M ;
SACCO, O ;
CAKIROGLU, AG ;
JACKSON, JF ;
RIFKIND, RA ;
MARKS, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) :5282-5286
[33]  
MICHAELI J, 1992, J BIOL CHEM, V267, P23463
[34]  
MICHAELI J, 1992, CANCER CHEMOTHERAPY, V13, P288
[35]  
MOTOKURA T, 1992, J BIOL CHEM, V267, P20412
[36]   A NOVEL CYCLIN ENCODED BY A BCL1-LINKED CANDIDATE ONCOGENE [J].
MOTOKURA, T ;
BLOOM, T ;
KIM, HG ;
JUPPNER, H ;
RUDERMAN, JV ;
KRONENBERG, HM ;
ARNOLD, A .
NATURE, 1991, 350 (6318) :512-515
[37]   G1 EVENTS AND REGULATION OF CELL-PROLIFERATION [J].
PARDEE, AB .
SCIENCE, 1989, 246 (4930) :603-608
[38]  
PIERCE GB, 1971, CANCER RES, V31, P127
[39]   HUMAN CYCLIN-A IS ADENOVIRUS E1A-ASSOCIATED PROTEIN-P60 AND BEHAVES DIFFERENTLY FROM CYCLIN-B [J].
PINES, J ;
HUNTER, T .
NATURE, 1990, 346 (6286) :760-763
[40]   NEW GROUP OF POTENT INDUCERS OF DIFFERENTIATION IN MURINE ERYTHROLEUKEMIA CELLS [J].
REUBEN, RC ;
WIFE, RL ;
BRESLOW, R ;
RIFKIND, RA ;
MARKS, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (03) :862-866