Table 2.
Cell lines and cancer tissues | K-ras mutationb | Alteration | Predicated products | Percentage of the mutation in pancreatic cancer tissues among 188 pancreatic cancer casesa |
---|---|---|---|---|
PANC-1 | Yes, codon 12 | GGT to GAT | GLY to ASP | 42.6 % (80/188) |
Capan-2 | Yes, codon 12 | GGT to GTT | GLY to VAL | 32.4% (61/188) |
MIA PaCa-2 | Yes, codon 12 | GGT to TGT | GLY to CYS | 1.1% (2/188) |
BXPC-3 | NO | NO | GLY | N/A |
HDF | NO | NO | GLY | N/A |
Pancreatic cancer patient #1c | Yes, codon 12 | GGT to GAT | GLY to ASP | N/A |
Pancreatic cancer patient #2c | Yes, codon 12 (two mutations) |
GGT to GAT GGT to TGT |
GLY to ASP GLY to CYS |
N/A |
Pancreatic cancer patient #5c | Yes, codon 12 | GGT to GTT | GLY to VAL | N/A |
Percentage of each K-ras codon 12 mutation in pancreatic cancer tissues was summarized from five studies.16, 26–29
Types of K-ras point mutation in PANC-1, Capan-2 and BXPC-3 cell lines were confirmed in our laboratory by sequencing genomic DNA, which was consistent with the previous reports.26,27
Presence of K-ras mutations in pancreatic cancer tissue samples collected in our laboratory was determined by mutant-enriched PCR as described in the Methods. N/A:Not applicable.