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. Author manuscript; available in PMC: 2011 Aug 28.
Published in final edited form as: Cancer Biol Ther. 2005 May 20;4(5):561–570. doi: 10.4161/cbt.4.5.1670

Table 2.

K-ras point mutations in pancreatic cancer cell lines and tissues.

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
a

Percentage of each K-ras codon 12 mutation in pancreatic cancer tissues was summarized from five studies.16, 2629

b

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

c

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.