Immunopositivity for Siglec-15 in gastric cancer and its association with clinical and pathological parameters.

The sialic acid-binding immunoglobulin-type lectin Siglec-15 is a promising target to cancer immunotherapy in several tumor types. The present study aimed to investigate Siglec-15 expression in gastric cancer (GC) patient tissue and to evaluate its clinical value. Siglec-15 expression was evaluated by immunohistochemistry with 71 patients. Siglec-15 staining was observed in tumor cells of 53 (74.64%) patients, with significant association with histologic classification and angiolymphatic invasion (p<0.05). Immunohistochemistry analysis also detected Siglec-15 in tumor-associated stroma cells (macrophages/myeloid cells). There was no significant association with outcomes parameters. Siglec-15 expression in well differentiated histological GC tissues and in the tumor microenvironment are potential targets to be further investigated as a novel prognostic factor for GC.

Introduction

Gastric adenocarcinoma (GC) is the fifth most common cancer globally.[1,2] Although there are well-established risk factors, the diagnosis of GC is often late, with a poor prognosis and advanced cases. There is an urgent need for new diagnostic and prognostic biomarkers for GC.[3] Glycosylation is an important post-translational modification for proteins and is associated with crucial roles in cells, such as differentiation, transformation, cell growth and immune surveillance and has been reported in several human diseases including cancer.[4,5] Changes in the glycosylation profile in cancer mainly result from changes in the size of the glycan, generally towards shorter O-glycans and more branched N-glycans. In addition they impact on the nature of terminal epitopes in glycan chains mediated by changes in the process of sialylation and fucosylation, and changes in the expression of glycosfingolipids.[6,7] Thus, the alterations in glycosylation have been recognized as a hallmark of cancer, with implications in carcinogenesis, angiogenesis, and metastasis.[8,9] Many tumor biomarkers used in the practical clinic are sialylated glycoproteins.[5]

Sialic acid plays an important role due to its size, hydrophilic characteristic and electronegative charge;[10] Siglecs, endogenous lectins that bind to glycans and regulate signal transduction, are expressed and have immunosuppressive properties on immune cells.[8] Siglec-15 is an immunoglobulin-like lectin that acts as a sialic acid binder and it can be overexpressed in many human cancers, including colon, kidney, liver, thyroid cancer.[11,12] A recent study showed that Siglec-15 suppresses T cell responses and may contribute to dysfunctional immunity in the tumor microenvironment, by functional regulation of macrophages, with high potential to become a target for immunotherapy.[5] The present study evaluated Siglec-15 in GC tissues and adjacent noncancerous tissues and investigated the association of this protein with clinicopathological parameters.

Materials and Methods

Patients and samples

We selected formalin-fixed, paraffin-embedded tissue samples from patients diagnosed with GC, histopathologically reexamined by pathologist who underwent surgical resection at the Pernambuco Cancer Hospital, between 2013 and 2016. The following variables were collected in medical charts: age, sex, tumor type, location, pathological staging, Lauren classification, treatment type, lymph node number and location, positive lymph nodes, recurrence, metastasis, and death. The present study included 71 patients, 24 female patients (33.80%) and 47 males (66.19%) with a mean age of 59.25±13.30 (range 30-89). According to the histological grade, 20 cases (28.16%) were classified as well differentiated (G1), 15 (21.12%) as moderately differentiated (G2), and 36 (50.70%) as poorly differentiated (G3). Regarding the surgical staging, most patients were at stage T3 (51 cases; 71.83%), 6 cases (8.45%) were at stage T1, 12 (16.90%) as T2, and only 2 (2.81%) at T4. All the clinicopathological characteristics of GC patients are presented in Table 1.

Table 1.

Association analysis of Siglec-15 expression with clinicopathological features of gastric cancer patients.

Clinicopathological features	Siglec-15 (+)			Siglec-153 (-)	p
	n (%)			n (%)
Age (years)
≥60	30 (42.25%)			6(8.45%)	0.1073
<60	23 (32.39%)			12(16.90%)
Sex
Female	17(23.94%)			7(9.86%)	>0.9999
Male	36(50.70%)			11(15.49%)
Surgery
Total gastrectomy	24(33.80%)			8(11.27%)	>0.9999
Partial gastrectomy	29(40.85%)			10(14.08%)
Neoadjuvant treatment
I	49(69.01%)			17(23.94%)
III	4(5.63%)			1(1.41%)	>0.9999
Surgical staging (TNM)
I - II	10(14.08%)			8(11.27%)	0.0566
III - IV	43(60.56%)			10(14.08%)
Surgical staging (TNM)
II	5(7.94%)			7(11.11%)	0.0075
III	42(66.67%)			9(14.29%)
Lymph node involvement
Yes	36(50.70%)			10(14.08%)	0.3979
No	17(23.94%)			8(11.27%)
Histological grade
GI + GII	32(45.07%)			3(4.23%)	0.0022
GIII	21(29.58%)			15(21.13%)
Chemotherapy
Yes	28(39.44%)			10(14.93%)	>0.9999
No	25(35.21%)			8(11.27%)
Radiotherapy
Yes	15(21.13%)			6(8.45%)	0.7676
No	38(53.52%)			12(16.90%)
Recurrence
Yes	15(20.29%)			1(1.41%)	0.0546
No	38(53.52%)			17(23.94%)
Lauren classification
Intestinal	28(41.18%)			6(8.82%)	0.1684
Diffuse	22(32.35%)			12(17.65%)
Angiolymphatic Invasion
Detected	25 (37.88%)			3(4.55%)	0.0412
Not detected	25 (37.88%)			13 (19.70%)
H. pylori infection
Yes	7(11.29%)	1(1.61%)	38(61.29%)		0.4267
No

TNM, tumor-node-metastasis.

Immunohistochemistry

Tissue sections of 4 μm taken from tissue array blocks underwent deparaffinization with xylol, alcohol rehydration and antigenretrieval using citrate buffer at 96oC for 15 min. After cooling to room temperature, the slides were blocked against endogenous peroxidase activity with 0.3% H[2]O[2] and 1% methanol solution. Following, the blockade of the non-specific bonds was made with bovine serum albumin 1% in Phosphate Buffer Saline (PBS). The sections were then incubated with rabbit polyclonal antibody against human Siglec-15, (Cusabio Technology, LLC, Wuhan, China, dilution 1:100) diluted in PBS/BSA 1% at 4°C overnight. Next, sections were incubated with the amplification system (Easylink On, ImmPRESS™, and Dako EnVision™) at room temperature for 1h was applied and the reaction was visualized with diaminobenzidine (DAB, Sigma-Aldrich). The positive control used was colon and prostate cancer tissue according to the antibody manufacturer’s designation (Cusabio Technology, LLC) and negative controls were produced by omitting the primary antibodies (Supplementary Figure 1).

Figure 1.

Immunohistochemical labelling for Siglec-15 in GC samples. A) Membrane staining (white arrow) and myeloid cells (blue arrow) in the microenvironment. B) Positive metaplasia. C) Cytoplasmic and nuclear staining (white arrow).

Image analysis

Histomorphological analysis were performed with an integrated image system (BIOPTICA B20) microscope coupled to a CMOS camera (2584 x 1936 pixels resolution) with ISCapture image capture software. The enzyme labeling site (cytoplasmic, membrane, and perinuclear and nuclear) were also analyzed. Combinations of associated clinical-pathological parameters and outcome parameters were made with enzyme labeling and labeling site. Semi-quantitative analysis of the stained cells was done using immunoreactive score (IRS) classification by analyzing 5 random fields in each slide.[13,14] IRS = SI (staining intensity) x PP (percentage of positive cells). Staining intensity was determined as 0 is negative; 1, weak; 2, moderate; and 3, strong. The percentage of positive cells was defined as 0 is negative; 1, 10% positive cells; 2, 11-50% positive cells; 3, 51-80% positive cells; and 4, more than 80% positive cells. The score evaluation was done by two independent evaluators through the analysis of images at 200x magnification.

Outcome analysis

Survival analyses were made accessing the differential expression for Siglec-15 available in the cBioPortal for Cancer Genomics (http://cbioportal.org). Differences in overall survival and relapse free time were evaluated through three cohorts.[15,16] Overall survival was defined from the day of the sample intake to the patient’s death. Data of the patients who had survived until the end of the observation period were censored at their last follow-up visit.

Statistical analysis

Fisher’s exact test was performed in GraphPad Prism version 7.0. A p-value of <0.05 was considered statistically significant. Analysis of outcome was evaluated through Kaplan-Meyer curves with a long-rank test. Multivariate logistic regression analysis was performed using STATA, with stepwise forward selection.

Results

Siglec-15 expression in gastric cancer

Siglec-15 was positively labeled in 53 patients (74.64%), 17 female patients (23.94%) and 36 (50.70%) males (Table 1). In neoplastic lesions, Siglec-15 was observed in the cytoplasm in 14 samples (26.41%), perinuclear in 4 (7.54%) and nuclear in 1 only sample (1.88%). On the other hand, combinations of cytoplasmic, nuclear and perinuclear staining were observed in 34 samples (61.9%) (Figure 1 A,B). IHQ analysis detected Siglec-15 not only in gastric cancer cells but in tumor-infiltrating macrophages (Figure 1A). In 40 samples (59.70%) of the 71 patients analyzed presented an adjacent normal tissue, in which 17 (42.5%) were SIGLEC-15 positive, especially in the ducts and in production cells of the gastric glands. Additionally, Siglec-15 was detected in 40.9% (9/22) of the preneoplastic lesion intestinal metaplasia (IM) (Figure 1C) and it was found significant association between Siglec-15 expression in GC compared to normal non-transformed and IM adjacent gastric tissue (Table 2). Regarding the Siglec-15 and its association with clinical-pathological parameters, its expression was significantly associated histologic classification (p=0.0022) and angiolymphatic invasion (p=0.041). Interestingly, Siglec-15 cellular location staining was also associated to the tumor-node-metastasis (TNM) stage (p=0.01). Patients with high TNM (III+IV; 66.04%) showed Siglec-15 staining in cytoplasm and multiple cellular compartments compared with patients with low TNM stage (I+II; 7.55%).

Table 2.

Paired comparison of Siglec-15 staining in neoplastic cells, non-transformed and metaplasia adjacent gastric tissue.

	Non-cancerous	Neoplastic	Metaplasia	p
Siglec-15 (+)	17	53	9	<0.0001
Siglec-15 (-)	40	18	13	<0.0001

Additional analysis, including age, sex, type of surgery, initial treatment, nodal status, radiotherapy, chemotherapy, lymph node, H. pylori infection and Lauren classification were not significant. In relation to overall survival, for Siglec-15 positive were 337 days and 501 days for the negative group (p=0.2692); to disease-free survival, negative e positive groups had a mean survival of 18 and 14.5 months, respectively (p=0.3929) and were not statistically significant (Figure 2). Siglec-15 was also confirmed as a predictor of histological grade in GC by multivariate analysis (Table 3), as well as Lauren Classification.

Figure 2.

Associations with the outcome parameters. Overall survival Siglec-15 (p=0.2692) (A) and disease-free survival (p=0.6852) (B), Overall survival (p=0.3799).

Table 3.

Univariate and multivariate Cox regression analysis of histological grade in GC patients.

	Univariate				Multivariate
Variable	OR	95%	CI	p	OR	95%	CI	p
Siglec-15	0.12	0.03	0.47	0.002	0.07	0.00	0.52	0.009
Lauren classification	0.04	0.01	0.14	0.000	0.02	0.04	0.12	0.000
Chirurgical stage	0.57	0.19	1.68	0.311	0.51	0.09	2.88	0.453

Discussion

In the present study, it was demonstrated for the first time that Siglec-15 expression was present in most CG cases. Siglecs have the role of distinguishing the self from the non-self-antigens and glycoprotein sialylation is a process that masks neoplastic cells during carcinogenesis.[17] The expression of Siglec-15 was significantly higher in the areas of metaplasia and neoplasia compared to areas of normal tissue. In cancer, the production of soluble mucins can negatively regulate the immune response, by binding with Siglecs receptors in Natural Killers cells, dendritic cells and monocytes.[18] In this way, the high expression of Siglecs reduces the innate immunity response against cancer cells by negatively regulating the immune response to sialylated antigens.

A study based on the TCGA database revealed that Siglec-15 is upregulated in many types of human tumors compared to normal tissues.[19] However, no significant differences were observed in cholangiocarcinoma, stomach adenocarcinoma, glioblastoma multiforme, and clear cell renal carcinoma. In our study, almost 75% of the total samples were Siglec-15 positive and 59.70% presented an adjacent normal tissue. Only considering this adjacent tissue, we found that 42.5% were Siglec-15 positive. Taking into account that Li et al.[19] have analyzed Siglec-15 mRNA expression from correspondent normal tissues whereas we focus on the characterization of Siglec-15 protein staining in GC tissues and adjacent areas, differences were already expected. This is because, as well as analyzed molecular levels (mRNA and protein), the nature of healthy samples (normal correspondent and adjacent tissue) is also different.

Wang et al. collaborators evaluated Siglec-15 in non-small cell lung cancer samples and found that this protein was present in both neoplastic cells and tumor-associated stromal cells.[5] In the present study, Siglec-15 was also detected in macrophages, corroborating the potential role of this protein in modulating the immune system. Recent studies have identified Siglec-15 as a potential new target for immunotherapy due to its immune suppressive role in tumor microenvironment.[5,20] These studies show that Siglec-15 is upregulated in neoplastic cells and overexpressed in macrophages and suppressor cells derived from the myeloid lineage, while few normal myeloid cells express Siglec- 15. Additionally, Takamiya et al. demonstrated that Siglec-15 is expressed in a subset of tumor-associated macrophages, in a coculture model with THP-1 cells (macrophages-derived) and H157 (human lung carcinoma).[21]

It would be interesting to evaluate the programmed status of ligand-1 death (PDL-1) in these GC samples to investigate whether the expression of Siglec-15 is mutually exclusive to that of PDL-1, as observed in lung adenocarcinoma.[5] Immunotherapy against cancer using PD-1/PD-L1 blockade has impacted the treatment of several neoplasms. However, these immunological checkpoints are responsible for only a partial dysfunctional immunity in human solid tumors and many patients who respond initially acquire resistance to these therapies with recurrent diseases. [22] Therefore, researching new immunological normalizers will increase the possibilities of immunotherapy against cancer. A phase I clinical trial is underway to assess the effect of humanized anti-Siglec-15 (NC318) on solid tumors and new findings are highly anticipated.

We demonstrate that the high expression of Siglec-15 was closely related to the most differentiated histological grade, maintained in the multivariate analysis. Siglecs abnormal expression is correlated with disease progression and prognosis in many cancer types, such as hepatocellular carcinoma, acute myelocytic leukemia and lung cancer.[23-26] In GC, low expression of intratumoral Siglec-8 was a significant negative prognostic factor for patients.[27] Since in Brazil the GC diagnosis is late and occurs in more advanced stages of disease, characteristic present in the cohort evaluated where 50% of patients had poorly differentiated GC, the higher expression of Siglec-15 observed in well and moderate differentiated compared to poorly differentiated GC, lead us infer that this expression can act as a good prognostic factor.

The high-affinity binding of Siglecs to mucins and N-glycosylated glycoproteins[28] has been associated with poor prognosis, [29] tumor progression inhibition of anti-tumor immune responses and metastasis.[30,31] In metastatic models, the Siglecs role in downregulation of NK cell cytotoxicity was associated with favorable circumstances for survival and metastasis while the use of the anti-Siglec antibody was related to prevention of the metastasis development and improved survival.[32,33] Despite the reports associated with metastasis, to our knowledge this is the first study to relate Siglec’s expression to angiolymphatic invasion indicating that further studies should be performed to establish the role of Siglec-15.

To date, there are no studies that have evaluated the expression of Siglec-15 according to the degree of differentiation of tumors. Thus, our data are precursors in demonstrating associations of this lectin with a well and moderately differentiated histological grade, with more advanced staging, and with angiolymphatic invasion. However, bigger investigations are needed to elucidate the role of Siglec-15 in of the tumor microenvironment, as well as in GC progression.