MATERIALS AND METHODS

Patients and tissue samples

Under the exclusion criteria described previously [34], 1,370 out of 1,853 CRC cases resected at Seoul National University Hospital, Seoul, Korea, between January 2004 and June 2008 were reviewed. Among them, 1,281 cases with formalin-fixed, paraffin-embedded (FFPE) tumor blocks sufficient for construction of a tissue microarray (TMA) were included in the study. Initial pathologic diagnosis and clinical information, including age, tumor location and radiologic/pathologic evidences of distant metastases were obtained from electronic medical records. Additional histologic parameters including tumor differentiation, tumor budding, representative number of tumor-infiltrating lymphocytes (TILs) per one high power field (400× magnification), were evaluated by two pathologists as described previously.34 FFPE tissues were used for molecular analysis and immunohistochemistry.

Immunohistochemistry

For each CRC case, a pair of 2-mm cores of representative tumor areas in the FFPE tissue were extracted to construct the TMA. To evaluate SMAD4 expression in CRCs, TMAs were sectioned at a thickness of 4-μm and stained using a rabbit monoclonal anti-SMAD4 antibody (1:200 dilution, clone EP618Y, Abcam, Cambridge, UK). Stained slides were scanned by an Aperio AT2 slide scanner (Sausalito, CA, USA) at 40× magnification with a resolution of 0.25 μm per pixel. The proportion and the intensity of SMAD4 staining in nuclear compartment were evaluated using TMA Assistant protocol of QuPath [35], open-source software for digital pathology image analysis. In detail, the intensity of SMAD4 staining in nuclear compartment was graded using intensity feature of nuclear diaminobenzidine (DAB) optical densities (OD). Because nuclear DAB ODs of entrapped nonneoplastic epithelium range from 0.2 to 0.6, intensity of nuclear SMAD4 staining of tumor cells were evaluated using following cut-offs: intensity 0, DAB OD<0.2; intensity 1, DAB OD≥0.2 and <0.6; and intensity 2, DAB OD≥0.6. Finally, each case was classified to SMAD4-loss (≥95% of tumor cells showed intensity 0), SMAD4-low (≥5% of tumor cells showed intensity 1, and <30% of tumor cells showed intensity 2), and SMAD4-high (≥30% of tumor cells showed intensity 2). For survival analysis, CRC cases were dichotomized to CRCs with SMAD4 loss and CRCs with retained SMAD4 (SMAD4-low and SMAD4-high). The evaluation method and cut-offs for the expression of cytokeratin 7 (CK7) (clone OV-TL, 12/30, Dako, Carpenteria, CA, USA), cytokeratin 20 (CK20) (clone Ks20.8, Dako), and nuclear protein CDX2 (clone EPR2764Y, ready-to-use, Cell Marque, Rocklin, CA, USA) were described previously [36]. All immunohistochemical procedures in this study were conducted with an automated immunostainer (BenchMark XT, Ventana Medical Systems, Tucson, AZ, USA).

Molecular analyses

Through histological examination, representative tumor portions were marked and then subjected to manual microdissection. The dissected tissues were collected into microtubes containing lysis buffer and proteinase K and were incubated at 55°C for 2 days. DNA from paraffin-embedded tissues was extracted, and the polymerase chain reaction (PCR) was performed. Direct sequencing of KRAS codons 12 and 13 and allele-specific PCR for BRAF codon 600 were performed as described previously [34]. The MSI status of each tumor was determined by evaluating five microsatellite markers (BAT25, BAT26, D2S123, D5S346, and D17S250) as standardized by the National Cancer Institute [37]. A fluorescent label was added to either the forward or reverse primer for each marker, and the PCR products were electrophoresed and analyzed. We classified MSI status as MSI-positive (instability at two or more microsatellite marker), and MSI-negative (no instability or instability at one marker). The CIMP status was evaluated by the MethyLight assay of eight markers (CACNA1G, CDKN2A [p16], CRABP1, IGF2, MLH1, NEUROG1, RUNX3, and SOCS1) [38]. We classified CRCs into CIMPnegative (0–4 methylated markers), CIMP-positive 1 (5–6 methylated markers), and CIMP-positive 2 (CIMP-P2) (7–8 methylated markers), as previously described [34].

Statistical analyses

SAS ver. 9.4 (SAS Institute Inc., Cary, NC, USA) and R software (http://www.r-project.org) were used for statistical analyses. Clinicopathological characteristics were compared between the three SMAD4 expression groups by use of chi-square test or Fisher exact test, as appropriate. Chi-square test for trend was used to compute p for trend. Survival curves after surgery were estimated with the Kaplan-Meier method, and differences in survival curves were tested with the log-rank test. All statistical tests were two-sided, and statistical significance was defined as p<.05.

Ethics statement

This study was approved by the Institutional Review Board which waived the requirement to obtain informed consent (IRB No. C-1502-029-647).

RESULTS

Clinicopathological and molecular correlation of nuclear SMAD4 expression in CRCs

Out of 1,281 CRC cases, 210 (16.4%) showed a loss of nuclear expression of SMAD4 (Fig. 1A). Among the remaining cases with retained SMAD4 expression, 942 cases (73.5%) showed low-level expression (Fig. 1B), while high-level expression was observed in 129 cases (10.1%) (Fig. 1C).

We then sought to identify clinicopathologic features showing gradual changes according to the loss or overexpression of SMAD4 (Table 1). With decreasing expression of SMAD4, tumors tended to show an infiltrative gross type, more frequent lymphovascular and perineural invasion, tumor budding, and lower TILs (all p<.001). Consequently, CRC cases showed significant associations with higher pT (p<.001) and pN (p<.001) category, and frequent distant metastasis (p=.001) as nuclear SMAD4 expression decreased. Notably, statistically significant increase of SMAD4 loss and concomitant decrease of SMAD4 expression was noted as TNM stage increased (p <.001) (Supplementary Fig. S1).

To identify molecular phenotypical correlates of such linear trends, we evaluated MSI, CIMP status, KRAS exon 2, BRAF codon 600, and immunohistochemical expression of CK7, CK20, and CDX2 (Table 2). With increasing expression of SMAD4, tumors tended to be more associated with MSI (p < .001), CIMP-P2 (p=.001), and MLH1 promoter methylation (p< .001). Interestingly, the expression of CK20 and CDX2 showed opposite trends with increasing SMAD2 expression; CDX2 expression was lost as nuclear SMAD4 expression increased (p= .001), while the expression of CK20 increased (p<.001).

Prognostic implication of SMAD4 loss in CRCs

A univariate survival analysis revealed that CRCs with a loss of nuclear SMAD4 expression exhibited a significantly worse 5-year progression-free survival (PFS) (p<.001) (Fig. 2A), and 7-year CSS (p=.001) (Fig. 2B). To explore whether there exists a differential prognostic effect of SMAD4 according to TNM stage, we performed the Kaplan-Meier analysis for each TNM stage subgroups (Supplementary Figs. S2, S3). In a stage-specific analysis, SMAD4 loss was associated with worse 5-year PFS (p = .019) in stage II CRCs, worse 5-year PFS (p = .055) and 7-year CSS (p=.011) in stage IV CRCs. In the multivariate Cox proportional hazard analysis, a loss of SMAD4 expression proved to be an independent prognostic factor for 5-year PFS (hazard ratio [HR], 1.27; 95% confidence interval [CI], 1.01 to 1.60; p=.042) (Table 3), and for 7-year CSS (HR, 1.45; 95% CI, 1.06 to 1.99; p=.022), after adjustment for TNM stage, tumor differentiation, adjuvant chemotherapy, and lymphovascular invasion.

DISCUSSION

To the best of our knowledge, this is the second largest study focusing on the clinicopathologic and prognostic implications of SMAD4 expression in CRC, and the largest in an Asian population. While the largest previous study was performed on 1,381 stage II or III CRC patients enrolled at a pan-European clinical trial for adjuvant chemotherapy [12], our cohort consisted of 1,281 retrospectively collected patients ranging from stage I to IV. By combining CIMP analysis with additional histologic features such as tumor budding and TILs, we identified the general expression status of SMAD4 and its association with clinicopathologic and molecular features of CRC.

Most previous studies evaluated SMAD4 expression based on two-tier classification: loss versus no loss, or low versus high expression [7,8,10,11,13-15,17,18,20]. Because of ambiguities in the definition of low expression, the reported prevalence of low-level SMAD4 expression varied significantly from 2.34% to 75.2%. On the other hand, studies that adopted a multi-tier classification reported relatively homogeneous results, with the prevalence of low-level SMAD4 expression ranging from 9.3% to 37.7% [6,9,12,16]. Considering the presence of an apparent loss, overexpression, and intermediate expression of SMAD4, we felt it more appropriate to use a three-tier classification (loss, low-level, and high-level) of SMAD4 expression. As a result, 16.4% of our cases were identified as SMAD4 loss, which falls within the range of previous reports.

Consistent with the previous studies [8-17], we observed a significant association between SMAD4 loss and higher pT and pN category, and frequent distant metastasis. Consequently, we confirmed the value of SMAD4 loss as a prognostic factor for poor CSS and PFS of CRC. In colonic epithelial cells, TGF-β signaling reduces proliferation and promotes apoptosis and differentiation [39]. Because SMAD4 translocates to the nucleus by forming a heterodimeric complex with SMAD2/3 that is phosphorylated by the activated TGF-β receptor [2], it is intuitive that the immunohistochemical loss of nuclear SMAD4 expression suggests a concomitant loss of TGF-β signaling, which leads to uncontrolled proliferative behavior.

Interestingly, we observed that some tumors overexpressed SMAD4 and those tumors tend to be MSI, CIMP-P2, and have their MLH1 promoter methylated. Along with the association between fungating gross type, these data collectively suggested an association between the sporadic MSI-high (MSI-H)/CIMP-high phenotype and overexpression of nuclear SMAD4. Although the meaning of SMAD4 overexpression is not straightforward, such a trend has been reported previously [9,12,40]. One possibility is that overexpression of SMAD4 in MSI-H tumors might be the consequence of a compensatory mechanism for mutational inactivation of the TGF-β signaling pathway; i.e., some machineries in the pathway, such as transforming growth factor β receptor II (TGFBR2) or activin type II receptor (ACVR2), are prone to mutations when mismatch repair is impaired [39]. At the same time, there are reports suggesting various bypass mechanisms to overcome such mutations [41-44]. Further mechanistic studies are needed to confirm this hypothesis.

A novel finding in our study was the gradual increase of CDX2 expression as nuclear SMAD4 increased, while CK20 showed the opposite trend. Although this is in contrast with our previous report that expression of both CK20 and CDX2 got lost according to CpG island methylation [34], the proportional relationship of CDX2 and SMAD4 is consistent with some previous reports. In stomach, it has been reported that SMAD4 can activate the promoter of CDX2, and knockdown of SMAD4 led to the decreased expression of CDX2 [45]. Concomitant loss of SMAD4 and CDX2 was also observed in colorectal juvenile polyps obtained from juvenile polyposis syndrome patients [46]. The loss of CK20 expression could be explained as a consequence of epithelial mesenchymal transition (EMT). It is known that switch of intermediate filaments from cytokeratin to vimentin occurs during EMT [47]. It has been reported that the immunohistochemical expression of SMAD4 was positively correlated with that of EMT-related transcription factors such as Snail-1 and Twist-1 [48], and silencing of SMAD4 inhibited EMT [49]. Consequently, an intriguing hypothesis emerges that overexpression of SMAD4 accompanied loss of CK20 by promoting EMT.

Consistent with a previous study [17], we observed a significant association between low TIL infiltration and SMAD4 loss. Although this could be a secondary effect of the MSI status, there are a series of reports on the correlation between SMAD4 loss and CCL15 expression [50-52]. These researchers demonstrated that the loss of SMAD4 upregulated CCL15, which resulted in recruitment of CCR1+ cells at the invasive front. CCR1+ cells are phenotypically myeloid-derived suppressor cells (MDSC) and express immunosuppressive molecules such as indoleamine 2,3- dioxygenase. Using mouse models, these researchers demonstrated that the loss of SMAD4 promoted pulmonary and hepatic metastasis through the CCL15-CCR1 axis. It is plausible that the MDSCs are also responsible for the lower TIL infiltration we observed for tumors with SMAD4 loss.

In conclusion, we confirmed the value of determining expression of SMAD4 immunohistochemically as an independent prognostic factor for CRC in general. Furthermore, we identified some histologic and molecular features that might be clues to elucidate the role of SMAD4 in colorectal tumorigenesis and progression. Further studies are needed to validate these findings with an independent large-scale series of CRC cases.

Electronic Supplementary Material

Fig. 1.

Nuclear expression of SMAD4 in colorectal cancers. Representative examples for the loss of expression (A), low-level expression (B), and high-level expression (C).

Fig. 2.

Kaplan-Meier survival curves according to the nuclear SMAD4 expression. (A) 5-Year progression-free survival. (B) 7-Year cancer-specific survival.

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Figure & Data

References

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