H. Fukushima et al., Association of matrilysin mRNA expression with K-ras mutations and progression in pancreatic ductal adenocarcinomas, CARCINOGENE, 22(7), 2001, pp. 1049-1052
The matrix metalloproteinase matrilysin has been implicated in the progress
ion of gastrointestinal and other cancers. The aim of this study was to exa
mine matrilysin mRNA expression and determine whether it is correlated with
K-ras mutations and/or progression of pancreatic carcinoma. Using the semi
quantitative reverse transcriptase-polymerase chain reaction (RT-PCR), we a
nalyzed 11 pancreatic cancer cell lines and 70 pancreatic adenocarcinoma ti
ssues for matrilysin mRNA expression. The results were correlated with clin
icopathological characteristics and K-ras mutations, Significant amounts of
matrilysin mRNA were detected in six of the eight cell lines with K-ras mu
tations but not in the three cell lines with wild-type K-ras, Matrilysin mR
NA was detected in 57 (81.4%) of the 70 tumor tissues and in all of the eig
ht liver metastases, but not in any of the adjacent nontumorous tissues. Ma
trilysin expression was significantly correlated with the size of tumor, tu
mor spreading, lymph node metastasis, advanced pathologic tumor-node-metast
asis stage and K-ras mutations. The relative amounts of matrilysin mRNA in
tumor tissues increased with increase in tumor stage and were highest in li
ver metastatic tumor tissues. Our results suggest that matrilysin, the expr
ession of which is correlated with K-ras mutations, plays a key role in tum
or growth and progression of pancreatic carcinoma.