Expression pattern of CK7, CK20, CDX-2, and villin in intestinal-type sinonasal adenocarcinoma
- 1Department of Pathology, University Health Network, Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto M4N 3M5, Ontario, Canada
- 2University of California, San Francisco, San Francisco, California 94143-0424, USA
- 3University of British Columbia, Vancouver, British Columbia V5Z 1M9, Canada
- Correspondence to: Dr B Perez-Ordoñez Department of Pathology, University Health Network, Princess Margaret Hospital, 610 University Avenue, Toronto, Ontario M4N 3M5, Canada;
- Accepted 2 March 2004
Background: Intestinal-type sinonasal adenocarcinoma (ITAC) is an uncommon neoplasm, which resembles adenocarcinoma of the gastrointestinal tract. ITAC occurs sporadically or in association with occupational exposure to hardwood dust and other agents.
Aims: To investigate the phenotype and possible pathogenetic mechanisms of primary sinonasal and nasopharyngeal adenocarcinomas by staining for cytokeratin 7 (CK7), CK20, CDX-2, and villin.
Methods: Twelve sporadic sinonasal and nasopharyngeal adenocarcinomas were stained with monoclonal antibodies to CK7, CK20, CDX-2, and villin. The ITACs were classified as papillary, colonic, solid, mixed, or mucinous types.
Results: The diagnosis of ITAC was confirmed in 10 cases: five were colonic type and five were papillary. One was a sinonasal papillary low grade adenocarcinoma, and one a papillary nasopharyngeal adenocarcinoma, and these tumours were CK7 positive, but CK20, CDX-2, and villin negative. All ITACs were positive for CK20, CDX-2, and villin, and six were CK7 positive. One ITAC had a focus of intestinal metaplasia away from the invasive carcinoma.
Conclusions: Sinonasal ITACs have a distinctive phenotype, with all cases expressing CK20, CDX-2, and villin. Most ITACs also express CK7, although a proportion of tumours are CK7 negative. ITAC seems to be preceded by intestinal metaplasia of the respiratory mucosa, which is accompanied by a switch to an intestinal phenotype. Although ITACs are morphologically similar, differences in cytokeratin expression patterns suggest two distinct types. The expression pattern of CK7, CK20, CDX-2, and villin positive may be useful in separating these tumours from other non-ITAC adenocarcinomas of the sinonasal tract and nasopharynx.
- CK, cytokeratin
- ITAC, intestinal-type sinonasal adenocarcinoma
- LGSA, low grade sinonasal papillary adenocarcinoma
- nasal cavity
- sinonasal tract
- intestinal-type adenocarcinoma
- nasal cavity
- keratin 7
- keratin 20
Intestinal-type adenocarcinomas (ITACs) of the nasal cavity and paranasal sinuses are uncommon tumours that occur sporadically or are associated with occupational exposure to hardwood and leather dusts, nickel, and possibly smoking.1,2 ITACs are clinically aggressive and generally present at an advanced stage, with an overall mortality of approximately 53%.2 Histopathological grading appears to be a significant prognostic indicator.1,3 The morphological appearance of these tumours is variable and may resemble normal small intestinal mucosa, villous adenomas, conventional colorectal adenocarcinomas, mucinous adenocarcinomas, and signet ring cell carcinomas.1,2,4 The similarities between ITAC and intestinal adenocarcinoma extend beyond the light microscopic level to ultrastructural and immunohistochemical characteristics.4–6 Several studies have attempted to determine whether immunohistochemical markers could be useful in distinguishing sinonasal ITACs from metastatic colorectal adenocarcinomas, and from other non-ITAC sinonasal adenocarcinomas.6–8
To gain further insight into the phenotype and possible pathogenetic mechanisms of sinonasal ITACs, we investigated the expression of keratin 7 (CK7), CK20, the intestinal cytoskeletal protein villin, and the homeobox gene product CDX-2 in a group of sporadic sinonasal and nasopharyngeal adenocarcinomas. The differential expression of CK7 and CK20 has been useful in determining the site of origin of many adenocarcinomas.9,10 Given that most (78%) adenocarcinomas of the upper gastrointestinal tract coexpress CK7 and CK20, and most colorectal adenocarcinomas are CK20 positive,9,10 we hypothesise that the CK7/CK20 staining pattern in ITAC will reflect differentiation toward intestinal staining profiles, rather than the usual CK7+/CK20− phenotype seen in normal upper respiratory mucosa.
CDX-2 is an intestine specific transcription factor product of the CDX-2 homeobox gene. This gene is involved at one of the earliest stages of intestinal differentiation and plays an essential role in the proliferation and differentiation of intestinal epithelial cells.11 CDX-2 expression is lineage specific and has been found in normal colonic and small intestinal mucosa, Barrett’s metaplasia and adenocarcinomas,12,13 gastric intestinal metaplasia and intestinal-type adenocarcinomas,14,15 and colorectal adenocarcinomas.16 Because the Schneiderian mucosa is of ectodermal origin and normally shows no evidence of intestinal differentiation, ITAC probably originates from intestinal metaplasia induced by hardwood dust, leather dust, and other unknown agents. The molecular mechanisms involved in metaplastic transformation of terminally differentiated epithelium to a phenotypically different epithelium are largely unknown; however, the intestinal phenotype of ITACs suggests that the CDX-2 gene is activated, so that these tumours should show consistent nuclear expression of the CDX-2 protein.
“To gain further insight into the phenotype and possible pathogenetic mechanisms of sinonasal intestinal-type sinonasal adenocarcinomas,
we investigated the expression of keratin 7 (CK7), CK20, the intestinal cytoskeletal protein villin, and the homeobox gene
Villin is a cytoskeletal protein required for the formation of brush border microvilli in the normal small intestine, colon, pancreatic ducts, biliary system, and proximal renal convoluted tubules. The restricted tissue expression of villin is conserved during neoplastic processes and an apical or brush border pattern of villin expression is seen in all gastrointestinal adenocarcinomas, even when their organised brush border structure is lost.17 Villin is also abundantly expressed in Barrett’s metaplasia and oesophageal adenocarcinoma.12 Villin expression in ITAC has not been studied as yet, but we also hypothesise that it should be uniformly positive in ITACs.
MATERIALS AND METHODS
Twelve cases of primary non-salivary gland-type adenocarcinoma of the sinonasal tract and nasopharynx were retrieved from surgical pathology files on the basis of an original pathological diagnosis of ITAC or non-salivary gland adenocarcinoma. Original haematoxylin and eosin stained slides were reviewed by two of the authors (MK and BP-O). A representative, formalin fixed, paraffin wax embedded block was selected for immunohistochemical studies using the antibodies listed in table 1. Villin and CDX-2 immunostains were performed manually with overnight incubation with the primary antibodies. Staining was completed using the ultrastreptavidin–horseradish peroxidase detection system (ID Labs Biotechnology, London, Ontario, Canada) and colour development was performed using the NovaRed substrate kit (Vector Laboratories, Burlingame, California, USA). Staining for CK7 and CK20 was performed in a Ventana BenchMark system (Ventana Medical Systems Inc, Tucson, Arizona, USA). The immunohistochemical stains were evaluated semiquantitatively and scored as: −, 0–5% positive cells; 1+, > 5–25% positive cells; 2+, > 25–50% positive cells; and 3+, > 50% positive cells. CDX-2 was regarded as positive if there was distinctive nuclear staining. Tumours with brush border membranous staining for villin were considered positive. All the tumours in which the diagnosis of ITAC was confirmed were subsequently subtyped, as described by Barnes,2 as papillary, colonic, solid, mixed, or mucinous types. Special attention was placed on the identification of Paneth cells and goblet cells. All tumours were investigated for the presence of squamous and intestinal metaplasia.
Ten patients were male and two were female. None of the patients had a known history of occupational exposure to hardwood dust. The age at presentation ranged from 21 to 87 years (mean, 63). Five tumours arose in the ethmoid sinus, three in the maxillary sinus, two in the nasal cavity, one in the sphenoid sinus, and one in the nasopharynx.
Morphological findings and immunohistochemistry
Table 2 shows the pathological types and immunohistochemical results. Five cases were classified as colonic type (fig 1A), five were papillary (fig 1B), and one was mixed, showing papillary architecture with abundant extracellular mucin production. One case was a low grade sinonasal papillary adenocarcinoma (LGSA) (fig 1C) and an additional case was a papillary nasopharyngeal adenocarcinoma (fig 1D). The cases classified as ITAC showed a variable cellular appearance and were composed of a mixture of tall columnar absorptive cells, atypical stratified cylindrical cells similar to the cells seen in conventional colorectal adenocarcinomas, goblet cells, and large round to polygonal non-descriptive epithelial cells. Paneth cells were seen in four cases and neuroendocrine cells with infranuclear cytoplasmic granules were readily seen in three. Of the tumours designated as ITAC, six were positive for CK7, CK20, CDX-2, and villin (fig 2). Four cases were negative for CK7 (fig 3), and positive for CK20, villin, and CDX-2. In summary, all tumours classified as ITACs were CK20 positive, villin positive, and CDX-2 positive, and six of 10 coexpressed CK7 and CK20. No differences in immunophenotype were seen between the papillary and colonic subtypes, or between those tumours with Paneth cells and those without. The papillary nasopharyngeal adenocarcinoma showed a distinctly different phenotype, and was positive for CK7 but negative for CK20, villin, and CDX-2. The non-ITAC LGSA was also CK7 positive and completely negative for CK20, villin, and CDX-2. The adjacent normal respiratory epithelium was positive for CK7, and negative for CK20, villin, and CDX-2.
Squamous metaplasia was identified in non-neoplastic mucosa in one patient. Intestinal metaplasia was present in one case (fig 4A). This focus of intestinal metaplasia was found 2 mm from carcinoma in situ and involved glandular epithelium. The metaplastic focus comprised atypical cylindrical epithelium and goblet cells, closely resembling a tubular adenoma of the colon. The metaplastic focus partially involved seromucous glands and was covered by morphologically normal surface ciliated respiratory epithelium. The focus of intestinal metaplasia was negative for CK7 and positive for CK20, CDX-2, and villin (fig 4B–D). The neighbouring non-metaplastic glandular and surface epithelia retained their CK7 positive phenotype, with lack of expression of CK20, CDX-2, and villin. The invasive adenocarcinoma associated with this area of metaplasia showed a similar phenotype.
We investigated the expression of CK7, CK20, CDX-2, and villin in 10 cases of ITAC, one LGSA, and a papillary adenocarcinoma of the nasopharynx. We found that all 10 cases of ITAC were positive for CK20 with six also coexpressing CK7. Furthermore, all 10 cases were also positive for CDX-2 and villin, demonstrating a distinctive intestinal phenotype. These results are in agreement with a small number of previous studies that investigated the expression of CK7 and CK20 in ITACs.7,8,18,19 Krane et al reported the coexpression of CK7 and CK20 in five cases of ITAC.18 Bashir et al also reported positive staining for CK7 and CK20 in three of their four cases of ITAC.7 The only case in the series by Bashir et al lacking CK20 staining was a colloid carcinoma, which incidentally was positive for CK7.7 Whether this tumour is indeed an example of ITAC is arguable because no additional stains such as CDX-2 and villin were performed. In a larger study, 15 ITACs reported by Franchi et al were also positive for both CK7 and CK20.19 Unlike these early reports, Choi et al found that some ITACs lack expression of CK7.8 These investigators found that all their seven cases of ITAC were positive for CK20; however, four lacked CK7 staining.8 Our results and the published literature show that all ITACs are consistently positive for CK20, and that most cases coexpress CK7 and CK20; however, we also confirmed the findings of Choi and colleagues8 that a smaller but significant proportion of ITACs possess a CK7−/CK20+ phenotype. Choi et al have suggested that coexpression of CK7 and CK20 results from a more rapid metaplastic transformation from respiratory epithelium to intestinal-type epithelium, whereas a longer transition time may allow time for the first set of cytokeratin genes to disappear and leave a solely CK20 positive profile.8 Thus, based on cytokeratin profiles, our results suggest that two divergent subsets of ITAC exist—one shows an expression profile similar to colorectal adenocarcinoma and the other resembles other upper gastrointestinal tract tumours. These findings may be useful for identifying differences in behaviour between the two groups, although a larger study with follow up is needed to determine this.
“Based on cytokeratin profiles, our results suggest that two divergent subsets of intestinal-type sinonasal adenocarcinoma
exist—one shows an expression profile similar to colorectal adenocarcinoma and the other resembles other upper gastrointestinal
CDX-2 is a transcription factor product of the CDX-2 homeobox gene. This gene is one of the earliest genes involved in intestinal differentiation and plays an essential role in the proliferation and differentiation of intestinal epithelial cells.11 CDX-2 expression is largely but not absolutely confined to adenocarcinomas of the gastrointestinal and pancreaticobiliary tracts.16 CDX-2 expression in tumours outside of the gastrointestinal tract includes mucinous adenocarcinomas of the ovary and adenocarcinomas of the urinary bladder.16 To the best of our knowledge, only one other study to date has investigated CDX-2 expression in sinonasal ITACs.19 Franchi et al demonstrated nuclear expression of CDX-2 in 15 cases of ITAC.19 Five tumours showed focal staining (5–10% of tumour cells), whereas the remainder showed diffuse positivity in > 50% of the tumour cells. CDX-2 staining was not present in normal respiratory mucosa or seromucous glands. In our study, using a similar antibody, we detected strong and diffuse nuclear expression of CDX-2 in nine of 10 cases. Only one case showed expression in 25–50% of the cells. As noted by Franchi et al, we found no CDX-2 staining in normal respiratory mucosa or seromucous glands.19
Villin is a cytoskeletal protein required for the formation of brush border microvilli in normal small intestine, colon, pancreatic ducts, biliary system, and proximal renal convoluted tubules. Villin expression is conserved in all gastrointestinal adenocarcinomas including colonic, gastric, pancreatobiliary, and Barrett’s oesophagus and adenocarcinomas.12,17 These tumours show a characteristic apical or brush border pattern of expression. Villin expression in ITAC had not been previously studied. In keeping with the distinctive intestinal appearance of ITAC, all of our patients showed strong apical staining for villin. Similar to CDX-2, no staining for villin was seen in normal mucosa or seromucous glands.
The differential diagnosis of ITAC includes LGSA,20,21 primary adenocarcinomas of the nasopharynx,22 and metastatic intestinal adenocarcinomas.23 In general, low grade sinonasal adenocarcinomas show tubulocystic or papillary patterns and are composed of a single layer of eosinophilic cuboidal or columnar cells. These tumours must be properly distinguished from ITAC because they have a much less aggressive clinical course and better prognosis.20,21 The distinction between typical ITAC and LGSA is based on the higher grade of most ITACs and their predominant cell population of cylindrical cells and goblet cells. However, this distinction can be difficult in low grade papillary ITACs. Our case of papillary nasopharyngeal adenocarcinoma was also difficult to distinguish from papillary ITAC because it contained a large number of mucous cells. However, the CK7 and CK20 profile and the expression of CDX-2 and villin were useful in distinguishing ITAC from these two non-ITAC adenocarcinomas. Both non-ITAC sinonasal and nasopharyngeal adenocarcinomas retained the CK7+/CK20−/CDX-2−/villin− phenotype of surface respiratory epithelium and seromucous glands. These results are mostly similar to the experience reported by Bashir and colleagues7 and Choi et al,8 who found that most ITACs were positive for CK20, with a small proportion coexpressing CK7 and CK20, whereas all non-ITACs were always negative for CK20 and positive for CK7.
Other than the two cases presented in our report, there is no previously published experience with CDX-2 and villin in non-ITAC sinonasal adenocarcinomas, but the consistent expression of these two antigens in adenocarcinomas of the gastrointestinal tract suggest that they are helpful in separating ITAC from other non-ITAC sinonasal and nasopharyngeal adenocarcinomas. Given the similarities between ITAC and colorectal adenocarcinoma, the expression of CK20, CDX-2, and villin does not seem to be useful for distinguishing primary ITAC from metastatic intestinal adenocarcinoma. The coexpression of CK7 and CK20 largely excludes a metastasis from a colorectal adenocarcinoma, but will not necessarily exclude metastases from gastric, oesophageal, or pancreatobiliary primaries.8,19
The identification of precursor lesions of ITAC is not only academically intriguing but also clinically important because it may allow early detection and surgical intervention in patients at increased risk as a result of occupational exposure. However, the identification of these putative preinvasive lesions has remained elusive and controversial. Several studies have reported an increased incidence of squamous metaplasia in woodworkers,24 whereas others have described goblet cell hyperplasia, cuboidal metaplasia,25 and cuboidal metaplasia with dysplasia.26 Kleinsasser and colleagues27,28 argue that ITACs arise de novo from “intraepithelial mucous glands” on the surface ciliated epithelium. The identification of a specific immunophenotype for ITAC may help in the identification of its precursor lesions. Choi et al found intestinal metaplasia in surface respiratory epithelium in four of their seven cases of ITAC.8 These metaplastic foci were accompanied by conversion from CK7 positivity to CK20 positivity. In our series, we also found a case with a focus of intestinal metaplasia. The metaplastic focus showed a phenotype (CK7−/CK20+/CDX-2+/villin+) similar to the invasive carcinoma, whereas the non-neoplastic mucosa retained its CK7+/CK20−/CDX-2−/villin− phenotype. Our observations and the results reported by Choi and colleagues8 suggest that the development of ITACs is preceded by intestinal metaplasia, with conversion from a normal CK7+/CK20−/CDX-2−/villin− phenotype to an abnormal CK7−/CK20+/CDX-2+/villin− intestinal phenotype. None of the previous studies describing the presence of cuboidal metaplasia and dysplasia in woodworkers investigated the immunophenotype of these putative preneoplastic lesions; however, the use of this group of antibodies may provide a better definition of these lesions and clarify their relation to ITAC. There is experimental evidence derived from studies in oesophageal keratinocytes with chronic acid exposure and gastric intestinal metaplasia that CDX-2 becomes activated,13,14,29,30 and possibly plays a crucial role in the development and maintenance of an intestinal phenotype. Additional genetic events such as p53 mutations, and p14 and p16 inactivation may be necessary for the development of invasive adenocarcinoma.31 Based on a review of the literature, we propose a hypothetical model of the pathogenesis of ITAC (fig 5). Further investigation of the possible role of certain genes and their products, such as CDX-2 and MUC2, in the mucosa of woodworkers seems warranted.
Take home messages
Sinonasal intestinal-type sinonasal adenocarcinomas (ITACs) have a distinctive immunophenotype—all cases express CK20, CDX-2, and villin
Most ITACs also express CK7, although a small but significant proportion do not
It appears that ITAC is preceded by intestinal metaplasia of the respiratory mucosa, which is accompanied by a phenotypic switch to an intestinal phenotype
The expression of CK7, CK20, CDX-2, and villin is useful in separating these tumours from other non-ITAC adenocarcinomas of the sinonasal tract and nasopharynx
“Our observations suggest that the development of intestinal-type sinonasal adenocarcinoma is preceded by intestinal metaplasia,
with conversion from a normal CK7+/CK20−/CDX-2−/villin− phenotype to an abnormal CK7−/CK20+/CDX-2+/villin− intestinal phenotype”
Sinonasal ITACs show a distinctive phenotype, with all cases expressing CK20, CDX-2, and villin. Most ITACs also express CK7; however, there is a small but significant proportion of tumours that lack staining for CK7. ITAC seems to be preceded by intestinal metaplasia of the respiratory mucosa, which is accompanied by a phenotypic switch to an intestinal phenotype. The expression of CK7, CK20, CDX-2, and villin is useful in separating these tumours from other non-ITAC adenocarcinomas of the sinonasal tract and nasopharynx.