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K-ras mutations in stools and tissue samples from patients with malignant and nonmalignant pancreatic diseases.

With a 5-year survival rate on the average <5%, pancreatic carcinomas are among the neoplasias with the worst prognoses (1). Because the disease is characterized by a long-term interval of nonspecific symptoms associated with an early appearance of mainly lymphogenic metastases, only a minority of patients can be treated by curative surgery at the time of diagnosis. However, the 5-year survival rates may exceed 20% if resections are performed at early tumor stages when the patients are free from infiltrated lymph nodes and perineural or duodenal invasion (2). Thus, earlier tumor detection is the major means of improving the prognosis for pancreatic cancers unless novel treatment approaches, e.g., gene or immune therapy, are broadly applicable.

Conventional tumor markers, such as CA 19-9, have a diagnostic sensitivity of >70%; however, they lack specificity and are poorly suited to reveal the initial stages of cancer progression (3). Because its potential to detect single neoplastic cells, PCR could be valuable in identifying curable pancreatic tumors provided appropriate genomic markers are available. A potential molecular marker for pancreatic cancers is K-ras. The K-ras protooncogene codes for a 21-kDa protein that belongs to a highly conserved family of GTPases involved in signal transduction (4, 5). When growth factor binds to receptor tyrosine kinases, Ras proteins become activated by an exchange of the associated guanine nucleotide GDP by GTP. Engaging several effectors, the best known of which is c-Raf, GTP-Ras initiates downstream cascades, eventually leading to the phosphorylation of key transcription factors. Oncogenic forms of K-Ras are permanently activated proteins that result from point mutations of the codons 12, 13, or 61. More than 80% of all pancreatic cancers harbor activated K-ras, with mutations being virtually restricted to codon 12 (6). This unique constellation simplifies analytical approaches and allows for mutant enrichment techniques (7). Furthermore, oncogenic K-ras occurs at early stages of tumor progression (8) and can be determined in a noninvasive manner by analyzing stool (9). Thus, the K-ras status in stool is a candidate test for screening persons at increased risk for pancreatic tumors, for example, elderly persons, [~80% of pancreatic cancers occur between the ages of 60 and 80 (10)], patients with chronic pancreatitis (11), or those with predisposing hereditary disorders, e.g., BRAC2 mutation carriers (12). To gain additional information on its diagnostic value, we have compared the K-ras status of stools with that of tissue samples and serum tumor markers CA 19-9 and CEA from patients suffering from pancreatic tumors and chronic pancreatitis.

Materials and Methods

PATIENTS AND DIAGNOSIS

Stools and tissue samples were obtained with informed consent of the patients. Histological diagnosis and tumor grading and staging were done according to the Union Internationale Contre le Cancer criteria (13). Pancreatic tumors are classified as follows: pT1, tumors restricted to the pancreas; pT2, tumor invasion into duodenum, bile duct, and/or peripancreatic tissue; or pT3, tumor invasion into stomach, spleen, colon, and/or major vessels. Involvement of regional lymph nodes is indicated by pN0 or pN1 and distant metastases by pM0 or pM1.

DNA PREPARATION

Resected pancreatic tissue, transferred into lysis solution, and stool samples were stored at -80[degrees]C. DNA from tissue samples was prepared using the InViSorb Genomic Kit II (InViTek) according to the manufacturer's protocol. Stool DNA was prepared by strictly following the protocol of Sidransky et al. (14) with the only modification that a Cleanmix kit (Frobel) was used instead of glass powder in the last purification step.

MUTANT-ENRICHED PCR

Sample DNA was amplified by mutant-enriched PCR. The principle of this method is to introduce a BstNI restriction site into the amplicons of wild-type (wt)coding K-ras by means of primers containing a mismatch to the wt K-ras sequence (7). An ensuing incubation with BstNI cleaves wt amplicons but leaves mutant PCR products intact. This way, the ratio of mutant to wt amplicons can be increased by two orders of magnitude. A second amplification step is added to produce the amounts of PCR products required for further analysis. Mutant enrichment was carried out as described (15) except that unlabeled forward primers (5'AAC-TTG-TGG-TAG-TTGGAG-CT 3') and 5' biotin-labeled reverse primers (5' GTT-GGA-TCA-TAT-TCG-TCC-AC 3'; Biotez) were used in the second amplification step. Each PCR run included blanks and a positive control containing 0.1% of K-ras-mutated SW 480 cells among wt-coding peripheral blood cells.

GENOTYPING

K-ras genotyping was performed by a reverse dot blot test essentially as described (15). Amplicons were diluted 1/100 in binding buffer (2 mol/L NaCl, 10 mmol/L Tris, 1 mmol/L EDTA, pH 7.5), and 50 [micro]L was added to each well of a strip of eight streptavidin-coated microwells (Boehringer Mannheim). The samples were immobilized by incubation for 15 min at room temperature, the solution was then aspirated, and 50 [micro]L of 0.2 mol/L NaOH was added for strand separation. After 15 min at room temperature, the wells were washed three times with phosphate-buffered saline containing 1 mL/L Tween 20. Single-stranded amplicons were hybridized with 3 pmol of 5' digoxigenin-labeled probes representing wt K-ras coding for glycine (GGT) at codnn 12 or mutated K-ras coding for alanine (GCT), arginine (CGT), aspartate (GAT), cysteine (TGT), serine (AGT), or valine (GTT) and measured luminometrically as described (15).

TUMOR MARKERS

The tumor markers CA 19-9 and CEA were determined by enzyme immunoassays using the Axsym system (Abbott). Cutoff values were 37 kilounits/L for CA 19-9 and 5 [micro]g/L for CEA.

Results

The total frequency of K-ras mutations in tumor samples was 86% (38 of 44 cases; Table 1). Of the 44 tumors analyzed, 35 were ductal adenocarcinomas, 24 were from cancers of the head or head/body, 8 were from the body or body/tail, and 3 were from the tail. Thirty-two of the thirty-five (91%) ductal adenocarcinomas harbored mutated K-ras. Among the non-ductal cancers, five of seven periampullary carcinomas and one cystadenocarcinoma exhibited mutated K-ras. The following mutations were identified: 18 (47%) were GGT[right arrow]GAT, 14 (37%) were GGT[right arrow]GTT, 4 (11%) were GGT[right arrow]CGT, 1 was GGT[right arrow]GCT/GTT, and 1 was GGT[right arrow]GAT/GTT. Three of five tissues samples from patients with chronic pancreatitis carried K-ras mutations (2 were GGT[right arrow]GAT, and 1 was GGT[right arrow]GTT).

Stools from 40 patients were analyzed. Mutated K-ras was seen in 10 of 25 (40%) of the patients with ductal adenocarcinomas, in 1 patient with cystadenocarcinoma, and in 2 of 6 patients with chronic pancreatitis. Nine of the detected mutations were GGT[right arrow]GAT transitions, four were GGT[right arrow]GTT transversions. No mutations were found in the stools from four patients with periampullary cancers, from three patients with endocrine tumors, and from one patient with a cystadenoma. Stools from six control persons without known pancreatic disease had wt K-ras (not shown).

Serum tumor markers CA 19-9 and CEA were increased in 31 of 40 (78%)and 14 of 36 (39%) of the patients with ductal adenocarcinomas and 5 of 7 and 2 of 8 of the patients with chronic pancreatitis, respectively.

Discussion

K-ras MUTATIONS IN MALIGNANT AND PREMALIGNANT PANCREATIC LESIONS

Genotyping of tissue samples revealed K-ras mutations in >90% of the ductal adenocarcinomas, a figure in the range reported repeatedly. Because ductal cancer is by far the most abundant pancreatic tumor, this finding illustrates an outstanding diagnostic sensitivity of K-ras, which is further underlined by the similar high frequency of K-ras mutations found in papillary cancers. The latter result is in accord with previous data from Stork et al. (16) but differs from other reports showing that <50% of these tumors harbor oncogenic K-ras (17-19). This discrepancy may be partly attributable to the analytical procedures applied. Tada et al. (17) and Scarpa et al. (18) looked for K-ras mutations in PCR products that had not been enriched for mutations. Such an approach requires at least several percent of the altered alleles to be detected; thus the detection limit of this method is at least one order of magnitude above the detection limit of allele-specific amplification or mutant-enriched PCR (7,16). Furthermore, in ampullary cancers the frequency of oncogenic K-ras might be correlated to the tumor size, (19) and all but one of the periampullary tumors analyzed here were at stage T2 or T3. Generally, the low incidence of nonductal pancreatic tumors compromises a statistically accurate estimation of any oncogene involvement. This caveat includes endocrine tumors of the pancreas where controversial findings regarding K-ras have also been reported (20, 21).

Confirming previous evidence (9, 22-26), we saw K-ras mutations in the tissue samples of three of five patients with chronic pancreatitis, which points to the limitations of the diagnostic value of K-ras for malignant pancreatic diseases despite its sensitivity. These data have been extended by recent studies demonstrating that oncogenic K-ras can occur even in the pancreatic ducts of individuals without definite pancreatic disorder (23, 25, 27). Importantly, however, in all these cases mutated K-ras was not found in nondiseased ductal epithelia but always associated with hyperplasia or atypia, apparently reflecting an involvement of the K-ras oncogene in the expression of precursor lesions of pancreatic cancers (28). The prevalence of such premalignant ductal abnormalities seems rather high; these abnormalities are estimated to afflict nearly 50% of the healthy elderly population (29), and according to the published data (22, 26-28), 20-60% of those lesions may harbor mutated K-ras. Obviously, these observations pose a diagnostic dilemma: K-ras mutations may help identify curable cancers only if detectable at early tumor stages, but the earlier the gene is involved in tumor progression, the lower the probability that it is associated with malignancy. The combination of K-ras and serum tumor markers probably will not resolve this dilemma, as illustrated by our finding that five of seven patients with chronic pancreatitis showed increased CA 19-9. A multiplex molecular tumor marker analysis seems the more promising way to improve the discrimination of malignant from premalignant lesions. The tumor suppressors p16, p53, and dpc4 are frequently inactivated in pancreatic carcinomas (29). Recently, these markers were analyzed in addition to K-ras, and it was seen that in 37 of the 39 pancreatic cancers more than one of the four genes was damaged (30). It would be interesting to check a similar pattern of genes in premalignant pancreatic ducts.

K-ras TESTS IN STOOL DNA

To the best of our knowledge, a paper by Caldas et al. (9) describes the only previous study in which K-ras status was analyzed in the stool of patients suffering from pancreatic diseases. Using a colony hybridization assay and probing with radiolabeled oligonucleotides, these authors found mutated K-ras in 5 of 11 adenocarcinomas, 2 of 3 periampullary cancers, and 1 of 3 patients with chronic pancreatitis. Overall, our results fit the data of Caldas et al. (9) well. On the basis of these results, the diagnostic sensitivity of K-ras in the stool for pancreatic cancers may be preliminarily estimated as 40%. This figure is equivalent to that of serum CEA but is considerably less than the sensitivity of serum CA 19-9 and less than one-half of that of K-ras in tumor tissue. It implies that a negative K-ras test in stool is not sufficient to exclude pancreatic cancer in situations of uncertain diagnosis, e.g., in problematic cases of chronic pancreatitis. The positive predictive value is compromised because K-ras mutations may originate from colorectal tumors (13) and, as discussed, from premalignant pancreatic lesions, as exemplified here by the two patients with chronic pancreatitis who carry oncogenic K-ras in the stool. One of these cases (patient 62) was striking because analysis of the patient's tissue sample missed mutated K-ras, whereas an endoscopic secretion revealed the GGT[right arrow]GAT transition seen in the stool. Comparable observations were made by Caldas et al. (9), who reported discrepancies of the K-ras status between microdissected ductal lesions and tumor tissues in all five cases where parallel determinations had been done. In one of their cases, K-ras mutations were present in stool and the dissected ductal lesion but not in the tumor sample. Constellations such as those resemble the detection of dysplastic cells harboring mutated K-ras in pancreatic secretions of tumor-free patients (25). The frequent presence of oncogenic K-ras in premalignant lesions suggests that even apparently healthy persons might have mutated K-ras in the stool. Thus far we have seen K-ras mutations only in the fecal samples from patients with carcinoma or chronic pancreatitis; however, Villa et al. (31), screening for patients at risk for colorectal carcinoma, identified 2 K-ras-positive cases in the stools from 15 persons with no apparent organic disease.

Given the lack of specificity and the limited diagnostic sensitivity, is it worthwhile to analyze K-ras in the stool from subjects who are suspect for pancreatic tumors? At the moment we would not definitely give a negative answer because of the following consideration: K-ras genotyping in the stool is a noninvasive test with no risk of complications. With regard to the extremely poor prognosis of pancreatic cancers, a test contributing to an even modestly increased number of patients who can be treated by curative surgery would mark a valuable improvement. Because of its early role in carcinogenesis and its applicability to mutation enrichment, K-ras may identify curable tumors or, in the case of premalignant lesions, be used as be a novel criterion defining a patient's risk for cancer development on the molecular level. However, because the clinically important differentiation between premalignant and malignant lesions cannot be made based solely on this gene, the application of K-ras tests in stools for tumor screening seems problematic at present. It is important to establish a marker combination of K-ras, p16, and p53 suited for the analysis of stool samples.

We greatly appreciate the technical assistance of Marion Bebenroth, Kathrin Lange, and Kerstin Oehlschlegel. Special thanks to Wolfgang Henke for critical reading of the manuscript. The study was supported by grant 573/97 from the Bundesministerium fur Wirtschaft.

Received April 2, 1998; revision accepted July 29, 1998.

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CHRISTOPH BERNDT, [1] * KATRIN HAUBOLD, [2] FRANK WENGER, [2] BRIGITTE BRUX, [1] JOACHIM MULLER, [2] PETER BENDZKO, [3] TIMO HILLEBRAND, [3] ECKHARD KOTTGEN, [1] and JURGEN ZANOW [2] ([dagger])

[1] Institute of Laboratory Medicine and Pathobiochemistry and (2) Clinic of Surgery, Medical Faculty Charite, Humboldt-University, Schumannstrasse 20/21, D-10117 Berlin, Germany.

[3] InViTek GmbH, Berlin Buch, 10362 Berlin, Germany.

* Address correspondence to this author at: Universitatsklinikum Charite, Campus Charite-Mitte, Institut fur Laboratoriumsmedizin und Pathobiochemie, Schumannstrasse 20/21, 10098 Berlin, Germany. Fax 049-30-2802-1400; e-mail christoph.berndt@charite.de.

([dagger]) Present address: Konigin-Elisabeth-Krankenhaus, Berlin Lichtenberg, 13125 Berlin, Germany.
Table 1. K-ras status and tumor marker concentrations of
patients with pancreatic diseases.

No. Diagnosis Classification Grade

1 Ductal adenocarcinoma pT1pNOpMO G2
2 Ductal adenocarcinoma pT2pNOpMO G1
3 Ductal adenocarcinoma pT2pNOpMO G2
4 Ductal adenocarcinoma pT2pNOpMO G2
5 Ductal adenocarcinoma pT2pNOpMO G2
6 Ductal adenocarcinoma pT2pNOpMO G2
7 Ductal adenocarcinoma pT2pNOpMO G2
8 Ductal adenocarcinoma pT2pNOpMO G2
9 Ductal adenocarcinoma pT2pNOpM1 G2
10 Ductal adenocarcinoma pT2pN1pM0 G2
11 Ductal adenocarcinoma pT2pNOpMO G2
12 Ductal adenocarcinoma pT2pN1pM0 G2
13 Ductal adenocarcinoma T2N1M0 G2
14 Ductal adenocarcinoma T2N1M0 G2
15 Ductal adenocarcinoma pT2pN1pM0 G2
16 Ductal adenocarcinoma pT2pN1pM0 G2
17 Ductal adenocarcinoma pT2pN1pM0 G3
18 Ductal adenocarcinoma pT2pN1pM0 G3
19 Ductal adenocarcinoma pT2pN1pM1 G2
20 Ductal adenocarcinoma pT2pN1pM1 G3
21 Ductal adenocarcinoma pT2pN1pM1 G3
22 Ductal adenocarcinoma pT2pN1pM1 G3
23 Ductal adenocarcinoma pT3pNOpMO G2
24 Ductal adenocarcinoma T3NOM0 G3
25 Ductal adenocarcinoma T3NOM0 ND
26 Ductal adenocarcinoma pT3pNOM0 ND
27 Ductal adenocarcinoma pT3pN1pM0 G2
28 Ductal adenocarcinoma pT3pN1pM0 G2
29 Ductal adenocarcinoma pT3pN1pM0 G2
30 Ductal adenocarcinoma pT3pN1pM0 G3
31 Ductal adenocarcinoma pT3pN1pM0 ND
32 Ductal adenocarcinoma T3N1M0 ND
33 Ductal adenocarcinoma T3N1M0 ND
34 Ductal adenocarcinoma T3N1M1 G2
35 Ductal adenocarcinoma T3N1M1 G3
36 Ductal adenocarcinoma pT3pN1pM1 ND
37 Ductal adenocarcinoma pT3pN1pM1 G2
38 Ductal adenocarcinoma pT3pN2pM0 G3
39 Ductal adenocarcinoma pT3pN2pM1 G1
40 Ductal adenocarcinoma pT3pN2pM1 G3
41 Ductal adenocarcinoma pT3pN2pM1 ND
42 Ductal adenocarcinoma ND ND
43 Cystadenocarcinoma pT2pNOpMO ND
44 Cystadenoma TONOMO NA
45 Papillary adenocarcinoma pT1pNOpMO G2
46 Papillary adenocarcinoma pT2pNOpMO G1
47 Papillary adenocarcinoma pT2pNOpMO G2
48 Papillary adenocarcinoma pT2pN1pM1 G2
49 Papillary adenocarcinoma pT3pN1pM0 G2
50 Papillary adenocarcinoma pT3pN1pM0 G2
51 Adenocarcinoma of the pT3pNOpMO G2
 distal bile duct
52 Neuroendocrine carcinoma pT1pN1pM1 G1
53 Insulinoma NA NA
54 Insulinoma NA NA
55 Chronic pancreatitis TONOMO NA
56 Chronic pancreatitis TONOMO NA
57 Chronic pancreatitis TONOMO NA
58 Chronic pancreatitis pTOpNOpNO NA
59 Chronic pancreatitis pTOpNOpNO NA
60 Chronic pancreatitis pTOpNOpNO NA
61 Chronic pancreatitis pTOpNOpNO NA
62 Chronic pancreatitis pTOpNOpMO NA

 K-ras K-ras CA 19-9, CEA,
No. tissue stool kilounits/L g/L

1 GAT wt 482 23.50
2 GTT wt ND (a) ND
3 wt NA 290 0.72
4 GAT NA 97 3.10
5 GTT wt 1247 0.86
6 GTT NA 30 1.87
7 GTT NA 182 3.02
8 GAT GAT 1868 4.69
9 CGT wt 398 3.98
10 GTT GTT 806 1.20
11 GGT wt 20 150 ND
12 GTT GTT 914 4.48
13 NA GAT 1123 1.79
14 GAT GAT 27 4.64
15 GAT NA 4 4.49
16 wt NA 3092 ND
17 GTT/GCT wt 147 5.27
18 GAT NA 261 2.48
19 GAT/GTT GAT 1578 ND
20 GAT wt 1019 ND
21 GTT wt 155 1.24
22 GAT NA 1507 11.50
23 GAT NA 781 2.74
24 NA wt 1074 2.68
25 NA GTT 3823 16.00
26 CGT NA 46 718 50.00
27 GTT NA 2 3.74
28 GTT wt 291 1.06
29 GTT wt ND ND
30 GAT wt 588 13.50
31 GTT NA 12 6.97
32 NA wt 8251 18.68
33 NA GAT 151 4.73
34 NA wt 2 10.90
35 NA GAT 12 107.70
36 GTT NA 1089 3.17
37 GAT NA 5978 17.30
38 GTT NA 3 14.10
39 GAT GAT 19 984 16.70
40 GAT NA 5155 3.49
41 wt NA 3429 1.15
42 CGT wt 2 5.80
43 GAT GAT 211 6.50
44 NA wt 4 0.71
45 GAT NA 38 1.15
46 GAT wt 5 1.89
47 GAT NA 48 1.47
48 wt wt 1568 2.31
49 GAT NA ND 1.24
50 GTT wt ND ND
51 wt wt 18 7.21
52 wt wt 11 0.88
53 NA wt ND ND
54 NA wt 28 0.63
55 NA wt ND 4.46
56 NA wt 16 6.18
57 NA wt 173 5.80
58 wt NA 4 1.65
59 GAT NA 39 0.54
60 GTT GTT 2.54 1.89
61 GAT wt 345 4.12
62 wt GAT 95 0.9

(a) ND, not determined; NA, not applicable/not available.
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Title Annotation:Molecular Diagnostics and Genetics
Author:Berndt, Christoph; Haubold, Katrin; Wenger, Frank; Brux, Brigitte; Muller, Joachim; Bendzko, Peter;
Publication:Clinical Chemistry
Date:Oct 1, 1998
Words:4029
Previous Article:Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disorders.
Next Article:Chemical mismatch cleavage combined with capillary electrophoresis: detection of mutations in exon 8 of the cystathionine [beta]-synthase gene.
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