Distinctive clinicopathological features of Ki-ras mutated colorectal cancers
Background and Objectives We explored the relationship between the mutation pattern of Ki‐ras and the clinicopathological features of colorectal cancers (CRCs). Methods Relationships between clinicopathological parameters and Ki‐ras mutation status were analyzed in 255 CRC patients using the chi‐squ...
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Published in | Journal of surgical oncology Vol. 94; no. 3; pp. 234 - 241 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.09.2006
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Subjects | |
Online Access | Get full text |
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Summary: | Background and Objectives
We explored the relationship between the mutation pattern of Ki‐ras and the clinicopathological features of colorectal cancers (CRCs).
Methods
Relationships between clinicopathological parameters and Ki‐ras mutation status were analyzed in 255 CRC patients using the chi‐square and student t‐tests. Kaplan‐Meier survival curves were compared using the log‐rank test.
Results
Ki‐ras mutation occurred in 43.9% of tumors, and 83% affected codon 12. The most frequent mutations were GGT‐>GAT (Gly‐>Asp) (37.5%), followed by GGT‐>GTT (Gly‐>Val) (31.3%), both in codon 12. The frequency of Ki‐ras mutation was similar for different tumor stages (38.2–47.8%). The mucin component of tumors was significantly associated with Ki‐ras mutation. The 4‐year overall and disease‐free survival was 61% and 54%, respectively, for patients with Ki‐ras mutated tumors, and 73% and 60% for patients with nonmutated tumors (not statistically significant). Patients with Ki‐ras mutated tumors had lower plasma folate (24 ng/dl) than those bearing nonmutated tumors (37 ng/dl). Patients with G‐>T Ki‐ras mutations had the lowest folate level (22 ng/dl), followed by those with G‐>A mutations (25 ng/dl).
Conclusions
Ki‐ras mutated colorectal tumors have a higher mucin production and higher differentiation, and are associated with lower plasma folate levels and a relatively poorer disease outcome. J. Surg. Oncol. 2006;94:234–241. © 2006 Wiley‐Liss, Inc. |
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Bibliography: | Veterans General Hospital-Taipei - No. VGH93-243; No. VGH94-47 ArticleID:JSO20438 ark:/67375/WNG-Z801446N-K istex:345154337833F380C00989DB15132472A14F117D ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-4790 1096-9098 |
DOI: | 10.1002/jso.20438 |