- Research article
- Open Access
- Open Peer Review
Expression analysis of carbohydrate antigens in ductal carcinoma in situof the breast by lectin histochemistry
© Korourian et al; licensee BioMed Central Ltd. 2008
- Received: 18 December 2007
- Accepted: 14 May 2008
- Published: 14 May 2008
The number of breast cancer patients diagnosed with ductal carcinoma in situ (DCIS) continues to grow. Laboratory and clinical data indicate that DCIS can progress to invasive disease. Carbohydrate-mediated cell-cell adhesion and tumor-stroma interaction play crucial roles in tumorigenesis and tumor aggressive behavior. Breast carcinogenesis may reflect quantitative as well as qualitative changes in oligosaccharide expression, which may provide a useful tool for early detection of breast cancer. Because tumor-associated carbohydrate antigens (TACA) are implicated in tumor invasion and metastasis, the purpose of this study was to assess the expression of selected TACA by lectin histochemistry on DCIS specimens from the archival breast cancer tissue array bank of the University of Arkansas for Medical Sciences.
For detection of TACA expression, specimens were stained with Griffonia simplicifolia lectin-I (GS-I) and Vicia vilosa agglutinin (VVA). We studied associations of lectin reactivity with established prognostic factors, such as tumor size, tumor nuclear grade, and expression of Her-2/neu, p53 mutant and estrogen and progesterone receptors.
We observed that both lectins showed significant associations with nuclear grade of DCIS. DCIS specimens with nuclear grades II and III showed significantly more intense reactivity than DCIS cases with nuclear grade I to GS-1 (Mean-score chi-square = 17.60, DF = 2; P = 0.0002) and VVA (Mean-score chi-square = 15.72, DF = 2; P = 0.0004).
The results suggest that the expression of VVA- and GS-I-reactive carbohydrate antigens may contribute to forming higher grade DCIS and increase the recurrence risk.
- Invasive Breast Cancer
- Nuclear Grade
- Lectin Histochemistry
- Average Progression Rate
- Tumor Nuclear Grade
Breast carcinoma is the most common malignancy and currently the second leading cause of cancer death in women in the United States. An increasing number of women choose more sensitive screening with digital mammograms and magnetic resonance imaging, which has ultimately resulted in dramatic increase in the diagnosis of ductal carcinoma in situ (DCIS) during recent years [1–4]. The majority of invasive breast cancers likely develop over extended periods of time from pre-invasive lesions such as DCIS and culminating in metastatic disease [5–9]. Untreated DCIS lesions develop into invasive breast cancer with an average progression rate of 43% as estimated by using the results of 8 different independent studies performed with a wide range of follow-up time .
An increased risk of a recurrence as DCIS or invasive cancer was associated with initial DCIS lesions that were larger than 10 mm or were of high or intermediate nuclear grade [10–14]. High nuclear grade of initial lesions and cancer recurrence were significantly associated with increased rates of metastasis and breast cancer death [15, 16]. Therefore, nuclear grade is used as a major determinant of therapy and medical treatment decision for DCIS patients [11, 17, 18].
Tumor initiation and growth is associated with modifications to the structure of glycan residues belonging to glycoproteins, glycolipids and proteoglycans present at the cell surface . Aberrant glycosylation, arising from dysfunction of glycosyltransferases and/or glycosidases, most often results in a shortening of the glycan chains or an over-expression of structures on cells that are normally absent or scarce. It is well-recognized that aberrant carbohydrate expression is relevant to tumor metastasis and poor prognosis for cancer patients [20–22].
A feature of adenocarcinoma cells is their high accumulation of an abnormal mucin carbohydrate-substitution pattern compared with mucin of normal epithelial cells. This phenomenon is observed in most types of human cancers including breast cancer [23–26]. The accumulation of carbohydrate structures reactive with Vicia vilosa agglutinin (VVA) and Griffonia simplicifolia lectin-I (GS-I) is closely associated with development, progression, and metastasis of breast adenocarcinoma [27–30]. VVA reacts with N-acetyl-galactosamine (GalNAc) residues of glycoproteins that are predominantly expressed on the mucin MUC1 [29, 31]. The expression of VVA-reactive epitopes has been linked to lymphatic invasion and lymph node metastasis in invasive breast cancer . GS-I lectin is a mixture of isolectins that bind to Galα1-3Gal and α-GalNAc terminal groups, which are involved in the formation of metastases in murine and human breast carcinomas [32–35].
Because the expression of cell surface carbohydrate structures reactive with VVA and GS-I lectins has been linked to invasive breast cancer and its metastatic potential, we hypothesized that the expression of TACA reactive with these two lectins may define an aggressive phenotype in DCIS. Therefore, the aim of this study was to assess the expression of breast-cancer-related TACA markers reactive with GS-I and VVA lectins in DCIS cases in order to evaluate their presence and determine their correlations with established tumor prognostic factors.
This retrospective study was conducted on archival tissue-array blocks from patients diagnosed with DCIS between 1990–2002 at the University of Arkansas for Medical Sciences. This study was approved by the University of Arkansas for Medical Sciences Institutional Review Board.
Follow up information was available on all patients ranging from 5 to 16 years. Patients' age, race and tumor characteristics including tumor nuclear grade and size were obtained from the pathology data base whenever possible. For the majority of cases immunohistochemistry results of the molecular markers Her-2/neu, p53 and the estrogen and progesterone receptors were also available in pathology files. For the majority of the cases, immunohistochemistry results of the molecular markers Her-2/neu, p53 and the estrogen and progesterone receptors were also available in the pathology files. Immunohistochemical studies for estrogen, progesterone and p53 were performed on the original blocks using antibodies from Ventana Medical Systems Inc. (Tucson, AZ). Anti ER clone 6F1, anti PR clone1A6 and anti-p53 clone Bp53-11 were used. Any tumor with greater than 10% positivity with estrogen and progesterone were recorded as positive. Any nuclear positivity for p53 was reported as positive. Benign breast tissue within the submitted sections was used as internal positive control according to the pathology protocols. Hercept test by Dako (Carpinteria, CA) was used for Her2-neu testing. The cases were scored according to the DAKO standards of reporting for this antibody. The tumor was reported as negative, if the tumor cells showed no or weak incomplete cytoplasmic membrane staining. They were reported as positive 2+, if the neoplastic cells showed complete cytoplasmic membrane staining in more than 10% tumor cells at weak or intermediate intensity and positive (3+), if the tumor cells showed complete strong cytoplasmic membrane staining. The pathologist on record (SK) reviewed all samples and verified the presence of DCIS on the core used for the analysis. The study conducted on total of 60 available DCIS cases.
Staining of tumor specimen with lectins was performed based on a previously described method . Briefly, formalin-fixed paraffin-embedded tissue were cut at four microns and deparaffinized. Heat-induced epitope retrieval was performed using 10× citrate buffer (Dako) in a Fisher Isotemp water bath at 95–99°C. Slides were cooled down for 20 minutes and rinsed in distilled water. Slides then were treated with PBS containing BSA (bovine serum albumin, 20 mg in 10 ml PBS) for 20 minutes. Slides were washed in PBS with added Calcium Chloride (0.06 g to 1000 ml PBS) for 10 minutes with agitation. Sections were then incubated with lectins (2 μg/ml, Vector Laboratories, Burlingame, CA) for 30 min in PBS + 0.2% BSA at room temperature (RT) and washed in PBS. Sections were then incubated with streptavidin-HRP (Vector Laboratories) for 15 min at RT followed by PBS wash. Sections were incubated with diaminobenzidine solution (DAB) for 5 min at RT, washed with distilled water, counterstained with hematoxylin, mounted, and examined under a light microscope. Cytospin slides of VVA and GS-I-positive breast cancer cell line (MDA-MB-231) were used for positive control. Stromal cells of the breast parenchyma did not show any positivity with either lectin. These types of cells were present in all cores and were used as negative internal control.
ELISA was performed as described elsewhere . Briefly, plates were coated with 4 μg/ml of carbohydrate probes attached to a polyacrylamide polymer (PAA) (GlycoTech Corporation, Rockville, MA) in carbonate-bicarbonate buffer at 4°C overnight. Biotinylated lectins were then added and incubated for 1 hour at 37°C, and binding was visualized with streptavidin-HRP (Sigma, St Louis, MO). Absorbance was read, using a Bio-Tek ELISA reader (Bio-Tek instruments, Inc, Highland Park, Vermont).
Scoring and statistical analysis
Tumor nuclear grade was determined using the Van Nuys grading system [17, 38]. The expression of carbohydrate antigens was scored using a four-point staining-intensity scale (from 0, negative; to 3+, strongly positive). The size of initial tumor prior to 1999 was estimated based on the available gross description and the archival slides. The size, measured or estimated, was further categorized as 1 (≤ 1), 2 (> 1 and ≤ 2), 3 (> 2 and ≤ 3), 4 (> 3 and ≤ 4) and 5 (> 4). Association of staining intensities of lectins with age, race, tumor size and grade, estrogen receptor (ER), progesterone receptor (PR), p53, and Her-2/neu was characterized using the Spearman coefficient of rank correlation (rs). Associations between staining intensities and other ordinal categorical variables were tested for statistical significance using the Mantel-Haenszel (MH) correlation chi-square test . Staining-intensity associations with Age (the only continuous variable) were tested for significance using the P values associated with the rank correlations. The significance level for correlation analyses was set at 0.5% alpha to adjust for the multiple comparisons without inflating Type II error. Staining-intensity associations with nuclear grade of DCIS were further charactserized by computing for each grade the average staining-intensity score as follows: Average score = 0 × (proportion negative) + 1 × (proportion 1+) + 2 × (proportion 2+) + 3 × (proportion 3+). Differences in average scores between grades were tested for significance using the extended Mantel-Haenszel mean-scores chi-square test . Recurrence-free survival (RFS) was also examined in grade I DCIS patients. RFS was measured from the year of diagnosis to the year of recurrence, or censored at last follow-up (2007) if no recurrence occurred by the end of the year; the one death in 1999 for unrelated cause was censored at death for competing risks. For association with RFS, staining intensities were dichotomized as negative (0) versus positive (1+ or higher), and assessed for significance using the log-rank test. Statistical analyses were conducted using SAS Version 9.1.3 (The SAS Institute, Cary, NC, USA).
Patient population and tumor characteristics
Characteristics of patients and tumors used for this study
Tumor size (cm)
> 1, ≤ 4
Specificity of lectins used
Expression of VVA and GS-I-reactive epitopes in DCIS
Correlation between prognostic markers, race, age, tumor grade and tumor size with GS-I and VVA expression levels IN DCIS patients
MH χ2 b
MH P b
N c total
N c AA
MH χ2 b
MH P b
N c total
N c AA
The belief that DCIS is a precursor of invasive breast cancer necessitates the search for finding specific DCIS-associated antigens to identify patients at greater risk for development of invasive cancer and recurrence. Many studies have examined molecular markers in DCIS that are used in clinical practice for invasive breast cancer [43–51]. An overall similarity is reported in the expression of these markers in DCIS and invasive cancer, but with no definite conclusion as to the relevance of these markers to tumor invasion, recurrence and progression.
To search for possible DCIS-associated molecular markers that recognize high-risk DCIS patients, we performed a lectin histochemical staining focusing on breast-cancer-relevant TACAs and evaluated their correlations with tumor prognostic factors. We observed positive correlations between the expression of VVA- and GS-I-reactive structures and tumor grade in DCIS patients. Because tumor grade is the most relevant pathologic determinant of disease with invasive potential, these data suggest that glycoconjugates containing these antigens are associated with invasiveness in DCIS. Tumor grade has been shown to predict prognosis using four gene-expression-based models (70-gene, wound response, two-gene ratio, and recurrence score)  and has been used as a major component in prognostic classification of DCIS [11, 17, 18]. The statistically significant positive correlations observed between the grade of DCIS and the expression of structures reactive with GS-1 and VVA suggest that these reactive antigens may define a phenotype for disease progression or DCIS transformation to invasive disease.
Lack of association of reactivity of either lectin with age and race indicates that reactive structures are independent of race and age. Together, these data suggest that histological evaluation of the expression of VVA- and GS-I-reactive TACAs may serve as phenotypic markers of not only high grade DCIS as defined by nuclear grade, but they may also define DCIS cases which are at high risk for recurrence. In support of this conjecture is the observation that of a total of 13 Low-grade (grade I) DCIS cases in our study, only seven were found positive for VVA lectin and interestingly five of these seven cases were diagnosed with recurrences later in their life. The data suggest that the expression of the lectin-reactive structures in DCIS may play a role in tumor relapse. Further studies targeting low-grade DCIS specimens are needed to make conclusive remarks.
The exact nature of reactive carbohydrates in our staining with VVA and GS-I lectins is not known. Our data confirms the specificity of both lectins. We observed that VVA binds to both α-GalNAc and β-GalNAc, which is consistent with data published by others . Specificity of GS-I to α-GalNAc and α-Gal structures is also reported in the literature [33–35, 53, 54]. However, the α-Gal epitope is supposed to be absent in humans, because of a lack of alpha1,3-galactosyltransferase activity [55, 56]. Therefore, the overall correlative nature, observed in this study, between staining of these two lectins suggests that they both may react with a single epitope on potentially many antigens. Consistently, our data indicate that the Tn antigen (α-GalNAc, an O-linked carbohydrate structure) is an overlapping epitope reactive with these two lectins. However, the fact that, at 0.5% alpha, VVA showed a significant correlation with Her-2/Neu, but GS-I did not, suggests that there may be a distinct nature of reactivity for these two lectins on breast cancer specimens. This data also suggests that Her-2/neu protein might be decorated predominantly with β-GalNAc-containing sugar chains rather than structures that contain α-GalNAc. In this regard, while VVA targets mostly O-linked carbohydrates, binding of GS-I lectin to human breast carcinomas may be related to other unknown antigens. Other investigators also reported the reactivity of α-Gal-specifc GS-I-B4 isolectin with human breast cancer tissues [22, 42], which suggests that even if there is no α-Gal expression, another reactive structure should exist on human tumors. Ito and coworkers , proposed that poly-N-acetyllactosamines of N-linked glycans contain GS-I-B4 specific epitope on human breast cancer cells. Obviously, the identity of GS-I reactive structures on human breast cancer cells is not clear at the present time and further efforts are needed to identify these antigens.
Our results suggest that the expression of VVA- and GS-I-reactive carbohydrate antigens may contribute to forming higher grade DCIS and increase the recurrence risk. Such carbohydrates might ultimately serve as viable targets for future development of novel therapeutic strategies aiming at early stage of breast cancer. However, the elucidation of their role in biology and patho-physiology of the disease, which needs further research, precedes such efforts. The data also support the hypothesis of using the expression of these structures as prognostic markers for early stage breast cancer that necessitate conducting further studies on much larger sample size of low-grade DCIS specimens with long follow-up time to establish whether low-grade DCIS with a specific glycomic profile can be subject to relapse more often than other tumors of the same category.
We thank Arkansas Breast Cancer Research Program and the Department of Pathology of the University of Arkansas for Medical Sciences for their support of this study.
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