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K-ras Gene Mutations: an Unfavorable Prognostic Marker in Stage I Lung Adenocarcinoma

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Journal Virchows Arch
Date 1994 Jan 1
PMID 8205351
Citations 3
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Abstract

Activation of K-ras gene by point mutations, a common finding in lung adenocarcinomas, has been suggested to decrease patient survival. We investigated 109 lung adenocarcinomas, mostly small, peripheral, stage I tumours (81/109) for presence of K-ras gene mutations at codons 12 and 13. Mutations were detected by denaturing gradient gel electrophoresis analysis of specific sequences amplified by polymerase chain reaction from DNA extracted from archival pathological material. Thirty-three of 109 (30.3%) tumours showed mutations at codon 12 (28/33, 84.8%) or 13 (5/33, 15.2%) of the gene. Mutations and type of nucleotide substitutions were differently distributed among cytological subtypes, being more prevalent among less differentiated (G2 and G3) tumours and among bronchial than bronchiolo-alveolar type adenocarcinomas. Survival analysis showed an adverse effect of K-ras mutation on survival, restricted to stage I tumours. Median survival for 81 stage I patients was 30 months for non-mutated tumours versus 20 months for mutated tumours (p = 0.016). Multivariate analysis showed that age of patient (p = 0.001) and K-ras mutation status (p = 0.04) were the only independent factors influencing survival significantly. These data strengthen the hypothesis that K-ras gene mutations may be useful in identifying a subgroup of patients with poor outcome.

Citing Articles

KRAS Mutation Is a Significant Prognostic Factor in Early-stage Lung Adenocarcinoma.

Kadota K, Sima C, Arcila M, Hedvat C, Kris M, Jones D Am J Surg Pathol. 2016; 40(12):1579-1590.

PMID: 27740967 PMC: 5106330. DOI: 10.1097/PAS.0000000000000744.


Wnt pathway activation predicts increased risk of tumor recurrence in patients with stage I nonsmall cell lung cancer.

Shapiro M, Akiri G, Chin C, Wisnivesky J, Beasley M, Weiser T Ann Surg. 2012; 257(3):548-54.

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The role of RAS oncogene in survival of patients with lung cancer: a systematic review of the literature with meta-analysis.

Mascaux C, Iannino N, Martin B, Paesmans M, Berghmans T, Dusart M Br J Cancer. 2004; 92(1):131-9.

PMID: 15597105 PMC: 2361730. DOI: 10.1038/sj.bjc.6602258.

References
1.
Sundaresan V, Ganly P, Hasleton P, Rudd R, Sinha G, Bleehen N . p53 and chromosome 3 abnormalities, characteristic of malignant lung tumours, are detectable in preinvasive lesions of the bronchus. Oncogene. 1992; 7(10):1989-97. View

2.
Pellegata N, Losekoot M, Fodde R, Pugliese V, Saccomanno S, Renault B . Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer. Anticancer Res. 1992; 12(5):1731-5. View

3.
Vahakangas K, Samet J, Metcalf R, Welsh J, BENNETT W, Lane D . Mutations of p53 and ras genes in radon-associated lung cancer from uranium miners. Lancet. 1992; 339(8793):576-80. DOI: 10.1016/0140-6736(92)90866-2. View

4.
Mitsudomi T, Steinberg S, Oie H, Mulshine J, Phelps R, Viallet J . ras gene mutations in non-small cell lung cancers are associated with shortened survival irrespective of treatment intent. Cancer Res. 1991; 51(18):4999-5002. View

5.
Sorensen J, Hirsch F, Olsen J . The prognostic implication of histopathologic subtyping of pulmonary adenocarcinoma according to the classification of the World Health Organization. An analysis of 259 consecutive patients with advanced disease. Cancer. 1988; 62(2):361-7. DOI: 10.1002/1097-0142(19880715)62:2<361::aid-cncr2820620222>3.0.co;2-m. View