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[Cancer Research 54, 1556-1560, March 15, 1994]
© 1994 American Association for Cancer Research

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K-ras and p53 Gene Mutations in Pancreatic Cancer: Ductal and Nonductal Tumors Progress through Different Genetic Lesions1

N. S. Pellegata, F. Sessa, B. Renault, M. Bonato, B. E. Leone, E. Solcia and G. N. Ranzani2

Department of Genetics and Microbiology, University of Pavia, 27100 Pavia, Italy [N. S. P., B. R., G. N. R.]; Department of Pathology, Ospedale di Circolo di Varese, 21100 Varese, Italy [F. S., M. B.]; Department of Pathology, Istituto di Ricovero e Cura a Carattere Scientifico-Ospedale S. Raffaele, Milano, Italy [B. E. L.]; Department of Human Pathology, University of Pavia and Istituto di Ricovero e Cura a Carattere Scientifico-Ospedale S. Matteo, 27100 Pavia, Italy [E. S.]

We studied K-ras and p53 gene mutations in a panel of 57 primary pancreatic cancers including ductal and nonductal tumors. DNAs were obtained from formalin-fixed, paraffin-embedded material. Target sequences were amplified by polymerase chain reaction and analyzed by denaturing gradient gel electrophoresis and sequencing. Both K-ras and p53 genes were frequently mutated in ductal cancers (25 of 35, 71.4%; 18 of 35, 51.4%, respectively). K-ras mutations were confined to the second position of codon 12 where base transitions and transversions were equally observed. p53 changes were mainly missense mutations. Transitions and transversions were found equally with a prevalence of G:C->A:T changes among transitions. No gene alterations were present in the 6 exocrine nonductal tumors and (with one exception) in the 12 endocrine tumors analyzed. Our results indicate that mutated K-ras and p53 genes can cooperate in the establishment of ductal pancreatic cancers, whereas other genetic events have to be present in nonductal tumors. Moreover, K-ras alterations may represent an early event in ductal tumorigenesis, as suggested both by the high gene mutation frequency and by the presence of mutations in low-grade tumors. On the contrary, p53 gene changes seem to represent an event required for the malignancy progression of ductal tumors from lower to higher grades.

1 This work was supported by a grant from the Ministero Università e Ricerca Scientifica to G.N.R.

2 To whom requests for reprints should be addressed, at Dip. di Genetica e Microbiologia, Via Abbiategrasso 207, 27100 Pavia, Italy.

Received 9/ 7/93. Accepted 1/14/94.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1994 by the American Association for Cancer Research.