TY - JOUR
T1 - Polyamine‐dependent expression of the matrix metalloproteinase matrilysin in a human colon cancer—derived cell line
AU - Wallon, U. Margaretha
AU - Shassetz, L. Richard
AU - Cress, Anne E.
AU - Bowden, G. Tim
AU - Gerner, Eugene W.
PY - 1994/11
Y1 - 1994/11
N2 - Matrilysin, which is a member of the matrix metalloproteinase family and is implicated in colon cancer invasion, is expressed in human colon adenocarcinoma—derived SW1116 cells. We investigated the effect of α‐difluoromethylornithine (DFMO) on matrilysin expression in this cell line because others have shown that DFMO can inhibit invasion and carcinogenesis in epithelial tissues, including the colon, in experimental models. DFMO reduced extracellular levels of matrilysin protein after 4 d of treatment. Intracellular levels of matrilysin protein were minimally affected by DFMO treatment. The decrease in extracellular matrilysin protein levels caused by DFMO was not a consequence of lowered steady‐state levels of matrilysin mRNA. After 4 d of exposure, the amount of this transcript was higher in DFMO‐treated cells than in untreated cultures, whereas the mRNA stabilities were similar. These data show that polyamine depletion by DFMO can suppress the expression of matrilysin, a gene product thought to be involved in tumor invasion. The decrease in extracellular matrilysin protein caused by DFMO treatment appears to be due to a posttranscriptional mechanism, although transcription of this gene also seems to be affected by polyamines in SW1116 cells. ©1994 Wiley‐Liss, Inc.
AB - Matrilysin, which is a member of the matrix metalloproteinase family and is implicated in colon cancer invasion, is expressed in human colon adenocarcinoma—derived SW1116 cells. We investigated the effect of α‐difluoromethylornithine (DFMO) on matrilysin expression in this cell line because others have shown that DFMO can inhibit invasion and carcinogenesis in epithelial tissues, including the colon, in experimental models. DFMO reduced extracellular levels of matrilysin protein after 4 d of treatment. Intracellular levels of matrilysin protein were minimally affected by DFMO treatment. The decrease in extracellular matrilysin protein levels caused by DFMO was not a consequence of lowered steady‐state levels of matrilysin mRNA. After 4 d of exposure, the amount of this transcript was higher in DFMO‐treated cells than in untreated cultures, whereas the mRNA stabilities were similar. These data show that polyamine depletion by DFMO can suppress the expression of matrilysin, a gene product thought to be involved in tumor invasion. The decrease in extracellular matrilysin protein caused by DFMO treatment appears to be due to a posttranscriptional mechanism, although transcription of this gene also seems to be affected by polyamines in SW1116 cells. ©1994 Wiley‐Liss, Inc.
KW - Polyamines
KW - colon cancer
KW - gene expression
KW - matrilysin
UR - http://www.scopus.com/inward/record.url?scp=0027997695&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027997695&partnerID=8YFLogxK
U2 - 10.1002/mc.2940110304
DO - 10.1002/mc.2940110304
M3 - Article
C2 - 7945802
AN - SCOPUS:0027997695
VL - 11
SP - 138
EP - 144
JO - Molecular Carcinogenesis
JF - Molecular Carcinogenesis
SN - 0899-1987
IS - 3
ER -