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(American Journal of Pathology. 2000;157:755-761.)
© 2000 American Society for Investigative Pathology

Regular Articles

Dpc-4 Protein Is Expressed in Virtually All Human Intraductal Papillary Mucinous Neoplasms of the Pancreas

Comparison with Conventional Ductal Adenocarcinomas

Christine A. Iacobuzio-Donahue^*, David S. Klimstra^§, N. Volkan Adsay^¶, Robb E. Wilentz^*, Pedram Argani^*, Taylor A. Sohn, Charles J. Yeo, John L. Cameron, Scott E. Kern^* and Ralph H. Hruban^*

From the Departments of Pathology,^*
Surgery,
and Oncology,
The Johns Hopkins Medical Institutions, Baltimore, Maryland; the Department of Pathology,^§
Memorial Sloan-Kettering Cancer Center, New York, New York; and the Department of Pathology,^¶
Wayne State University, Detroit, Michigan

	Abstract

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DPC4 (MADH4, SMAD4) encodes a nuclear transcription factor shown to be genetically inactivated in over one-half of conventional infiltrating ductal adenocarcinomas of the pancreas. Intraductal papillary mucinous neoplasms (IPMNs) of the pancreas have been suggested to be distinct neoplasms with a significantly less aggressive course than conventional ductal adenocarcinomas of the pancreas, but molecular comparisons of these tumor types have previously been impaired by technical difficulties. Recently, immunohistochemical labeling for the DPC4 gene product has been shown to be an extremely sensitive and specific marker for DPC4 gene alterations in pancreatic adenocarcinomas. Therefore, we analyzed the immunohistochemical expression of Dpc4 protein in 79 IPMNs using a previously characterized monoclonal antibody. Twenty-nine of the IPMNs also had an associated infiltrating adenocarcinoma available for analysis. The labeling patterns observed were compared to those we have previously reported for conventional ductal carcinomas. All 79 of the intraductal components of the IPMNs strongly expressed Dpc4 protein. In 77 of the 79 cases (97%), the labeling was diffusely positive, and in 2 of the 79 (3%) the labeling was focally positive. Dpc4 expression was seen in 28 (97%) of the associated 29 invasive cancers. The one infiltrating carcinoma that showed loss of Dpc4 expression was associated with an intraductal component which showed focal loss of Dpc4 expression. The strong and almost universal expression of Dpc4 in IPMNs contrasts sharply with the loss of Dpc4 expression seen in approximately 30% of in situ adenocarcinomas of the pancreas (so-called pancreatic intraepithelial neoplasms, grade 3; P < 0.001) and in 55% of pancreatic duct carcinomas (P < 0.0001). Differences in Dpc4 expression between IPMNs and ductal carcinomas suggest a fundamental genetic difference in tumorigenesis, which may relate to the significantly better clinical outcomes observed for IPMNs.

	Introduction

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DPC4 (MADH4, SMAD4) is a tumor-suppressor gene on chromosome 18q which has been shown to mediate the downstream effects of TGF-ß superfamily signaling, resulting in growth inhibition.^17,18 DPC4 is genetically inactivated in approximately 55% of pancreatic adenocarcinomas.^19-21 Inactivation of the DPC4 tumor-suppressor gene is relatively specific for pancreatic adenocarcinoma, although it has been shown to occur in a small percentage of primary carcinomas of the breast, ovary, colon, and biliary tract.^20-24 Wilentz et al have recently shown that immunohistochemical labeling for the Dpc4 protein is an extremely sensitive and specific marker for DPC4 genetic alterations,²⁵ thus providing a simple test for DPC4 gene status in archival material.

We analyzed a large series of IPMNs and their associated infiltrating carcinomas using this previously characterized antibody to the DPC4 gene product. By analyzing Dpc4 expression in this large series of IPMNs, we sought to determine the role of DPC4 in the genetic progression of this distinctive pancreatic neoplasm. The pattern of Dpc4 expression in IPMNs was also compared to that recently reported for in situ (pancreatic intraepithelial neoplasia (PanIN) grade 3) and infiltrating conventional ductal adenocarcinomas of the pancreas.²⁶

	Materials and Methods

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Specimen Selection

Pancreaticoduodenectomy (Whipple resections), distal pancreatectomy, and total pancreatectomy specimens from 79 patients with IPMNs were collected from the files of The Johns Hopkins Hospital (n = 36), Memorial Sloan-Kettering Cancer Center (n = 31), and Wayne State University (n = 12). Eleven pancreatectomy specimens included in the study had positive surgical resection margins. Pancreatectomy specimens included in the study were submitted in their entirety if no evidence of infiltrating carcinoma was found at the time of intraoperative consultation. If infiltrating carcinoma was found on intraoperative consultation, representative samples were submitted of the IPMN and associated infiltrating component. Clinical and pathological data were obtained from the patients’ medical records, The Johns Hopkins Hospital surgical pathology files, The Memorial Hospital for Cancer and Allied Diseases surgical pathology files, and The Detroit Medical Center surgical pathology files. Clinical and pathological variables included age, gender, race, tumor size, tumor location, grade of epithelial dysplasia, presence or absence of an invasive carcinoma, histological subtype of invasive carcinoma, presence of nodal or distant metastases, and survival. Pancreaticoduodenectomy specimens containing conventional infiltrating ductal adenocarcinomas and PanINs were collected, examined, and reported previously.^25,26

Grading of Dysplasia

Dysplasia in the slides labeled for Dpc4 expression was graded based on criteria established by the World Health Organization by three of the authors (R. H. H., N. V. A., and D. K.).¹⁵ The intraductal component of each tumor was categorized into adenoma, borderline, or carcinoma in situ. Three cases were categorized as intraductal oncocytic papillary neoplasms (IOPN) and were included in the carcinoma in situ subset. Adenomas were those tumors with tall, columnar, mucin-containing epithelial cells showing slight or no atypia. The epithelium of adenomas was either papillary or nonpapillary. Borderline tumors were those with moderate epithelial atypia, having nonpapillary or papillary epithelium with moderate cytologic atypia including loss of polarity, nuclear crowding, nuclear enlargement, pseudo-stratification, and nuclear hyperchromatism. Papillary areas maintained identifiable stromal cores. Those designated as carcinoma in situ were those intraductal tumors with severe dysplastic epithelial changes. IOPNs were characterized by a papillary growth pattern, with the papillary structures lined by stratified oncocytic cells with pale pink cytoplasmic granules (finer than those seen in Paneth cells) and interspersed goblet cells.²⁷ Carcinomas contained papillary or micropapillary structures, with cribriform growth and budding of small clusters of epithelial cells into the lumen. Epithelial changes were seen as loss of polarity, loss of mucin content, cellular and nuclear pleomorphism, nuclear enlargement, and the presence of mitoses. If an invasive carcinoma was identified adjacent to the intraductal component of an IPMN or IOPN, it was separately categorized as either colloid (mucinous noncystic carcinomas) or tubular (resembling usual ductal adenocarcinomas) type.¹⁵

Immunohistochemistry

The hematoxylin and eosin-stained slides from each of the 79 cases were screened by light microscopy for sections having IPMN, associated infiltrating carcinoma (if present), and adjacent normal pancreas. Unstained 5-µm sections were then cut from the paraffin block selected for each case and deparaffinized by routine techniques. Next, slides were treated with 1x sodium citrate buffer (diluted from 10x heat-induced epitope retrieval buffer, Ventana-Bio Tek Solutions, Tucson, AZ) before steaming for 20 minutes at 80°C. Slides were then cooled 5 minutes before incubating with a 1:100 dilution of monoclonal antibody to Dpc4 protein (clone B8, Santa Cruz Biotechnology, Santa Cruz, CA; 1:100 dilution) using the Bio Tek-Mate 1000 automated stainer (Ventana-Bio Tek Solutions). Finally, anti-Dpc4 antibody was detected by adding secondary antibody followed by avidin-biotin complex and 3,3'-diaminobenzidine chromagens. Sections were counterstained with hematoxylin.

Each immunolabeling procedure included an infiltrating pancreatic ductal adenocarcinoma previously shown to contain at least one wild-type DPC4 allele as a positive control, and a negative control pancreatic ductal adenocarcinoma with a known homozygous deletion of DPC4.^20,28

Immunohistochemical Evaluation

Immunohistochemical labeling of Dpc4 was evaluated by three of the authors (C. I.-D., R. H. H., and R. E. W.), with agreement in all cases examined. The immunolabeling pattern of each case was scored as positive, weakly positive, or negative. Tumors scored as positive showed strong, diffuse cytoplasmic labeling of the tumor epithelium, with scattered immunopositive nuclei also identified. Tumors scored as weakly positive showed only faint cytoplasmic labeling of tumor epithelium, with scattered positive nuclei also present. Tumors scored as negative showed no detectable cytoplasmic or nuclear Dpc4 protein. Positive and weakly positive cases were combined into a positive category for statistical analysis. The extent of immunolabeling was also categorized as diffuse (if the entire neoplasm labeled) or focal (if focal loss of expression was noted).

Normal pancreatic ducts, islets of Langerhans, pancreatic acini, lymphocytes, and stromal fibroblasts, all which had moderate expression of the DPC4 gene product, served as a positive internal control in each of the sections.

Statistical Analysis

Summary data are expressed as the mean ± SD unless otherwise indicated. When comparing differences between distributions, the ² test was used with additional confirmation using the Fisher exact test for sample sizes less than 5. Probability values of 0.05 or less were considered significant.

	Results

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Clinicopathological Characteristics

Clinicopathological characteristics of available data of the 79 patients with an IPMN are shown in Table 1 . The mean age of the patients was 69.5 ± 8.4 years, including 40 males and 34 females; in 5 cases the gender was not given. Fifty-three cases (73%) were located in the head and/or body, 10 (14%) primarily in the tail, and 10 (14%) involved the entire length of the pancreatic duct (head, body, and tail). In 6 cases the location was not specified.

Follow-up data were available for 35 of 37 patients with invasive IPMNs, and for 38 of the 42 patients with noninvasive IPMNs (mean/median follow-up, 28.7/19.0 months). Two patients with invasive IPMNs and four patients with noninvasive IPMNs died within 1 month of surgery of other causes, leaving postoperative survival data on 67 patients (33 patients with an invasive IPMN and 34 patients with a noninvasive IPMN). Among those 33 patients with invasive IPMNs, 8 of 33 (24%) had died, compared to only 2 of 34 (6%) patients with noninvasive IPMNs. Although a trend was observed, no significant differences in survival between these two groups were found (P = 0.07). All 8 of 8 patients (100%) who died with an invasive IPMN died of their disease, and 1 of these 8 had a positive surgical resection margin. The 2 patients who died with noninvasive IPMNs also died of their disease. One of these patients had an IPMN with borderline epithelial dysplasia which extended to the surgical resection margin, and the other had an IPMN with carcinoma in situ and no information available on this patient’s surgical resection margins.

Dpc4 Immunohistochemical Staining of the Intraductal Components of the IPMNs

The intraductal components of virtually all of the IPMNs labeled strongly for Dpc4. In 77 (97%) of the 79 IPMNs, the intraductal component of the neoplasm labeled diffusely positive (Figure 1, A and B) . In the remaining two IPMNs (3%) labeling of the intraductal component for Dpc4 was focally positive (Figure 2) . Dpc4 immunohistochemical staining was found in the intraductal component in all five adenomas, all of 18 borderline tumors, 51 of 53 carcinoma in situ, and all 3 IOPNs. The two IPMNs with focal labeling of the intraductal component for Dpc4 protein were both IPMNs with carcinoma in situ (Figure 2, A -C).

View larger version (109K): [in this window] [in a new window]   Figure 1. Dpc4 protein immunolabeling in the intraductal component of an intraductal papillary mucinous neoplasm (IPMN) and its associated infiltrating carcinoma. A: Strong and uniform Dpc4 expression in an IPMN with carcinoma in situ. B: Higher power view of an IPMN with carcinoma in situ, showing intense cytoplasmic and nuclear labeling in the epithelium. C: Infiltrating colloid carcinoma with intense Dpc4 labeling. D: High power view of an infiltrating colloid carcinoma, demonstrating strong positive labeling of the neoplastic cells in a mucin pool.

View larger version (113K): [in this window] [in a new window]   Figure 2. Heterogeneous Dpc4 protein immunolabeling in an IPMN with carcinoma in situ and an associated infiltrating tubular carcinoma. A: Low power view of an IPMN with carcinoma in situ, demonstrating focal intense expression (right side) and focal loss of expression (left side). B: Higher power view of the area expressing DPC4 in A. C: Higher power view of the area showing loss of DPC4 expression in A. D: High power view demonstrating loss of DPC4 expression in the infiltrating tubular carcinoma that arose in association with IPMN shown in A-C.

Twenty-nine of the IPMNs immunohistochemically analyzed for Dpc4 expression were associated with an invasive carcinoma, which was also available for labeling with the anti-Dpc4 antibody. Diffuse positive labeling of Dpc4 was seen in both the intraductal and infiltrating components in 27 of 29 (93%) of these IPMNs (Figure 1, C and D) . In the remaining two cases, the intraductal component of the IPMN had focal labeling for Dpc4, with clear-cut areas of the intraductal component showing loss of expression (Figure 2) . One of the two infiltrating carcinomas associated with these focally labeling IPMNs labeled positive, whereas the other infiltrating carcinoma was negative for Dpc4 protein expression (Figure 2D) . Thus, Dpc4 expression was identified in a total of 28 of the 29 infiltrating carcinomas (97%).

Dpc4 labeling of the invasive components of the IPMNs was also evaluated with respect to the morphology of the invasive component. All 19 infiltrating colloid carcinomas showed intense positive labeling for Dpc4 protein (100%), whereas 9 of the10 (90%) infiltrating tubular carcinomas showed positive labeling. In 4 of these 9 infiltrating tubular cancers, this labeling was weak. One infiltrating tubular carcinoma was negative for Dpc4 expression (Figure 2D) .

Relation of Dpc4 Immunohistochemical Staining to Clinicopathological Data

Clinical and pathological data of the 79 IPMN and 29 associated infiltrating carcinomas were collected and analyzed with respect to Dpc4 expression. Because of the almost universal expression of Dpc4 in the IPMNs, no significant differences in any clinical or pathological characteristic were identified with respect to Dpc4 protein expression.

Comparison of Dpc4 Expression in Intraductal Components of IPMNs to PanINs

We have previously reported studies of Dpc4 expression in conventional infiltrating ductal adenocarcinomas of the pancreas and in PanINs, the presumed precursor lesions to infiltrating ductal adenocarcinomas.^25,26 We therefore had a unique opportunity to compare the pattern of Dpc4 expression in IPMNs to the pattern of expression seen in the more aggressive conventional ductal adenocarcinomas. In a previous report, we examined Dpc4 protein expression in 188 PanINs from 40 pancreaticoduodenectomy specimens resected at The Johns Hopkins Hospital.²⁶ In this series, Dpc4 protein expression was found to be a marker of pancreatic neoplastic progression.²⁶ All low-grade PanINs (PanIN-1A, -1B, and -2) expressed Dpc4 protein, whereas 31% of the high-grade PanINs (PanIN-3, carcinoma in situ) did not. Although the overall frequency of Dpc4 labeling in the intraductal component of the IPMNs seen in the present study did not differ significantly from that seen in PanINs (79/79 IPMNs were positive for Dpc4 vs. 179/188 of PanINs; P = n.s.), there was a significant difference in Dpc4 expression when the IPMNs with carcinoma in situ (51/53) were compared to PanINs with carcinoma in situ (20/29; P < 0.001).

Comparison of Dpc4 Expression in Infiltrating Carcinomas Associated with IPMNs to Conventional Infiltrating Ductal Adenocarcinomas

We have previously reported our experience with Dpc4 protein expression in 39 infiltrating conventional ductal adenocarcinomas of the pancreas.²⁵ Dpc4 labeling was observed in 17 of 39 conventional infiltrating pancreatic ductal carcinomas (44%). By contrast, 28 of 29 (97%) infiltrating carcinomas associated with IPMNs labeled positively for Dpc4 (P < 0.0001).

	Discussion

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IPMNs are distinctive neoplasms of the pancreas characterized by dilatation of the pancreatic duct and/or its branches and by replacement of the duct epithelium by columnar, mucin-containing neoplastic epithelial cells, which form papillary or pseudopapillary structures.^4,14 Although several advances have been made in the understanding of the molecular genetics of conventional infiltrating pancreatic ductal adenocarcinomas, little is known of the genetic alterations that occur in IPMNs. Activating point mutations in the K-ras oncogene have been reported in 40 to 60% of IPMNs, HER-2neu overexpression in 75%, and the accumulation of the p53 gene product in 50%.^14,29-33 More recently, Fujii et al demonstrated frequent LOH at several chromosomal loci in IPMNs, with some IPMNs also showing genetic evidence of clonal progression.¹⁶ The DPC4 tumor-suppressor gene on chromosome 18q appears to play an important role in the development of conventional infiltrating ductal carcinomas of the pancreas and LOH at 18q was observed in 38% of the IPMNs examined by Fujii et al.^{16,17,20,21,34,35} Fujii et al, however, did not examine the remaining allele of the DPC4 gene, and functional DPC4 status could not, therefore, be determined in these tumors.

Recently, a sensitive and specific immunohistochemical stain for the DPC4 gene product has been developed.²⁵ We examined the expression of Dpc4 protein in 79 IPMNs, of which 29 had an associated invasive adenocarcinoma available for study. The intraductal components of the IPMNs uniformly and strongly expressed Dpc4 in 77 of the 79 (97%) cases. Focal expression of Dpc4 was seen in two of the 79 intraductal components of the IPMNs. Remarkably, Dpc4 protein expression was detectable in 28 of the 29 (97%) associated infiltrating carcinomas. This pattern of Dpc4 expression was significantly different from the pattern we have previous reported in high grade PanINs (P < 0.001) and in conventional infiltrating ductal adenocarcinomas (P < 0.0001). Approximately 70% of high grade PanINs and only 45% of infiltrating conventional adenocarcinomas show intact Dpc4 protein expression.^25,26

The almost universal immunodetection of Dpc4 in intraductal IPMNs and their associated infiltrating carcinomas suggests that genetic inactivation of DPC4 is an uncommon event in this distinctive neoplasm of the pancreas. Furthermore, in our previous series in which we examined Dpc4 expression in conventional ductal adenocarcinomas of the pancreas, there was a trend toward longer survival in the carcinomas which expressed Dpc4.²⁵ We can therefore hypothesize that the prolonged and indolent clinical course of IPMNs compared to conventional pancreatic duct carcinomas may be related in part to the persistant expression of Dpc4 in IPMNs.^4,5,10,11

The intraductal components of two IPMNs were particularly interesting in that they showed only focal positive labeling for Dpc4 with a portion of the intraductal IPMN showing clear loss of Dpc4 protein expression (Figure 2) . Similarly, LOH at chromosome 18q has been reported to be occasionally focal in IPMNs.¹⁶ In one of these focally negative IPMNs, the associated infiltrating tubular carcinoma was also negative for Dpc4. This finding suggests that in a small percentage of IPMNs, Dpc4 inactivation may occur in the progression to infiltrating carcinoma, similar to the findings of Fujii et al, who also demonstrated clonal genetic progression in IPMNs.¹⁶

Sixty-six percent of the infiltrating carcinomas in this study were colloid carcinomas and 33% were tubular carcinomas. All 19 colloid carcinomas showed strong and diffuse positive labeling for DPC4, whereas only 5 (50%) of 10 tubular carcinomas showed intense Dpc4 staining. Four (40%) of the 10 tubular carcinomas had weak labeling, and 1 (10%) had a loss of labeling. The finding of intense and uniform Dpc4 expression in these colloid carcinomas of the pancreas parallels observations made in the colorectum. Kern et al performed a detailed allelotype on a panel of colorectal carcinomas and found that mucinous carcinomas have less frequent allelic deletions of chromosome 18q than do conventional nonmucinous adenocarcinomas of the colorectum.³⁶

In summary, we report evidence that DPC4 inactivation, detected as loss of Dpc4 protein expression, is an infrequent event in IPMNs. This contrasts with the important role that DPC4 inactivation has been shown to play in the progression of conventional pancreatic ductal adenocarcinoma. Retention of Dpc4 expression in IPMNs may contribute to the indolent nature of these neoplasms, as compared to conventional ductal adenocarcinomas of the pancreas. However, further studies are warranted to determine the specific genetic events that are important in the progression of IPMNs. As these genes are characterized, they may aid in our understanding of the better prognosis associated with this distinct pancreatic neoplasm and, indirectly, help us to understand the course and consequences of the genetic progression model in pancreatic ductal neoplasia.

	Footnotes

 
Address reprint requests to Ralph H. Hruban, M.D., Meyer 7–181, Department of Pathology, The Johns Hopkins Hospital, 600 N. Wolfe Street, Baltimore, MD 21287. E-mail: rhruban{at}jhmi.edu

Supported by the National Institutes of Health Specialized Program in Research Excellence (SPORE) in gastrointestinal cancer grant CA62924.

Accepted for publication June 6, 2000.

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