Loss of LKB1 Protein Expression Correlates with Increased Risk of Recurrence and Death in Patients with Resected, Stage II or III Colon Cancer.
AMP-Activated Protein Kinase Kinases
Adaptor Proteins, Signal Transducing
/ genetics
Adult
Aged
Chemotherapy, Adjuvant
Colonic Neoplasms
/ genetics
DNA-Binding Proteins
/ genetics
Down-Regulation
Endonucleases
/ genetics
Female
Humans
Male
Middle Aged
Mutation
Neoplasm Staging
Oxaliplatin
/ administration & dosage
Protein Serine-Threonine Kinases
/ metabolism
Proto-Oncogene Proteins B-raf
/ genetics
Proto-Oncogene Proteins c-myc
/ genetics
Proto-Oncogene Proteins p21(ras)
/ genetics
Pyrimidines
/ administration & dosage
Survival Analysis
Treatment Outcome
BRAF
LKB1
MSI
Prognosis
Stage II-III
ΚRAS
Journal
Cancer research and treatment
ISSN: 2005-9256
Titre abrégé: Cancer Res Treat
Pays: Korea (South)
ID NLM: 101155137
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
02
01
2019
accepted:
17
03
2019
pubmed:
28
3
2019
medline:
19
2
2020
entrez:
28
3
2019
Statut:
ppublish
Résumé
The purpose of this study was to investigate the prognostic significance of liver kinase b1 (LKB1) loss in patients with operable colon cancer (CC). Two hundred sixty-two specimens from consecutive patients with stage III or high-risk stage II CC, who underwent surgical resection with curative intent and received adjuvant chemotherapy with fluoropyrimidine and oxaliplatin, were analyzed for LKB1 protein expression loss, by immunohistochemistry as well as for KRAS exon 2 and BRAFV600E mutations by Sanger sequencing and TS, ERCC1, MYC, and NEDD9 mRNA expression by real-time quantitative reverse transcription polymerase chain reaction. LKB1 expression loss was observed in 117 patients (44.7%) patients and correlated with right-sided located primaries (p=0.032), and pericolic lymph nodes involvement (p=0.003), BRAFV600E mutations (p=0.024), and TS mRNA expression (p=0.041). Patients with LKB1 expression loss experienced significantly lower disease-free survival (DFS) (hazard ratio [HR], 1.287; 95% confidence interval [CI], 1.093 to 1.654; p=0.021) and overall survival (OS) (HR, 1.541; 95% CI, 1.197 to 1.932; p=0.002), compared to patients with LKB1 expressing expressing tumors. Multivariate analysis revealed LKB1 expression loss as independent prognostic factor for both decreased DFS (HR, 1.217; 95% CI, 1.074 to 1.812; p=0.034) and decreased OS (HR, 1.467; 95% CI, 1.226 to 2.122; p=0.019). Loss of tumoral LKB1 protein expression, constitutes an adverse prognostic factor in patients with operable CC.
Identifiants
pubmed: 30913862
pii: crt.2019.008
doi: 10.4143/crt.2019.008
pmc: PMC6790836
doi:
Substances chimiques
Adaptor Proteins, Signal Transducing
0
DNA-Binding Proteins
0
KRAS protein, human
0
MYC protein, human
0
NEDD9 protein, human
0
Proto-Oncogene Proteins c-myc
0
Pyrimidines
0
Oxaliplatin
04ZR38536J
BRAF protein, human
EC 2.7.11.1
Protein Serine-Threonine Kinases
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
STK11 protein, human
EC 2.7.11.1
AMP-Activated Protein Kinase Kinases
EC 2.7.11.3
ERCC1 protein, human
EC 3.1.-
Endonucleases
EC 3.1.-
Proto-Oncogene Proteins p21(ras)
EC 3.6.5.2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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