Expression of IFITM1 as a prognostic biomarker in resected gastric and esophageal adenocarcinoma
© Borg et al. 2016
Received: 9 February 2016
Accepted: 4 May 2016
Published: 14 May 2016
There is an increasing amount of reports on IFITM1 (interferon-inducible transmembrane protein 1) in various malignancies. The aim of this study was to examine the expression of IFITM1 and its prognostic significance in gastroesophageal adenocarcinoma.
Tissue samples were obtained from a consecutive cohort of 174 patients surgically treated between 2006 and 2010 for gastroesophageal (gastric, gastroesophageal junction and esophageal) adenocarcinoma, not subjected to neoadjuvant therapy. Expression of IFITM1 was examined using immunohistochemistry on tissue microarrays of primary tumors and paired samples of adjacent normal epithelium, intestinal metaplasia and lymph node metastases.
Expression of IFITM1 was significantly elevated in primary tumors and lymph node metastases compared to adjacent normal epithelium and intestinal metaplasia, regardless of tumor location. Overexpression of IFITM1 was associated with M0-disease (no distant metastases). In gastric cancer IFITM1 expression was significantly associated with improved TTR (time to recurrence) in Kaplan-Meier analysis and Cox regression, both in the unadjusted analysis (HR 0.33, 95 % CI 0.12-0.88) and in the adjusted analysis (HR 0.32, 95 % CI 0.12-0.87) but there was no significant impact on OS (overall survival). In esophageal adenocarcinoma expression of IFITM1 had no impact on TTR or OS in Kaplan-Meier-analyses, but in the adjusted Cox regression IFITM1 expression had a negative impact on both TTR (HR 3.05, 95 % CI 1.09-8.53) and OS (HR 2.71, 95 % CI 1.11-6.67).
IFITM1 was overexpressed in gastroesophageal adenocarcinoma and associated with M0-disease. In gastric cancer IFITM1 expression had a positive impact on TTR but in esophageal cancer it seemed to have an adverse impact on survival.
The reason for the diverging prognostic impact of IFITM1 in esophageal and gastric cancer is unclear and warrants further studies.
KeywordsEsophageal neoplasms Stomach neoplasms Adenocarcinoma Prognosis IFITM1
Gastroesophageal adenocarcinoma is the 5th most common cancer worldwide . The incidence of esophageal and GE (gastroesophageal) junction adenocarcinoma has drastically increased in many Western countries for the last four decades [2, 3]. Suggested factors to explain this increase are gastroesophageal reflux disease, obesity and decreased prevalence of Helicobacter pylori infection [4, 5]. In contrast, the incidence of gastric adenocarcinoma has declined globally for several decades , possibly due to decreased prevalence of Helicobacter pylori infection and improved dietary conditions .
The prognosis of gastroesophageal adenocarcinoma is generally poor, at least in Western populations. For operable patients with resectable tumors recent studies have shown that the addition of neoadjuvant and/or adjuvant chemotherapy or chemoradiotherapy improves the 5-year survival rate with 10–15 % [8–11]. To further improve the overall survival in gastroesophageal adenocarcinoma, a deepened understanding of the tumor biology is required. Moreover, identification of prognostic and response predictive biomarkers is warranted to optimize and personalize the treatment strategies.
IFITM1 (interferon-inducible transmembrane protein 1), also known as 9–27, Leu-13 or CD225, is a cell surface 17-kDa membrane protein that is encoded on the short arm of chromosome 11. It is mainly known as an inhibitor of viral entry and replication , but it has also been associated with angiogenesis , inflammatory bowel disease  and osteogenesis .
There are now emerging data on IFITM1 and its role in malignancy. An upregulation of IFITM1 in different types of cancer and promotion of tumorigenesis by enhancing tumor cell migration, invasion and proliferation has been reported in several studies [16–23] but the opposite has also been shown [24–26]. Overexpression of IFITM1 has been reported to correlate with improved survival in glioma and chronic myeloid leukemia [17, 27] but in a South Korean study on gastric cancer, there was a trend towards worse survival in patients with high expression of IFITM1 . Apart from the latter study, the knowledge on IFITM1 in gastroesophageal cancer survival is very limited, especially in Western populations. Therefore, the current study was designed to explore the expression and prognostic significance of IFITM1 in adenocarcinoma of the esophagus, GE junction and stomach in a consecutive cohort of patients from southern Sweden, that were treated 2006–2010, prior to the wide implementation of (neo-)adjuvant oncological treatment.
Study design and participants
Patient and tumor characteristics
(n = 174)
(n = 60)
(n = 45)
(n = 69)
Number of examined nodes
Intestinal metaplasia background
Using a semi-automated arraying device (TMArrayer™, Pathology Devices, Westminster, MD, USA) tissue microarrays (TMAs) were constructed. From all 174 primary tumors duplicate cores (1 mm) were obtained from areas with morphologically viable cancer in different blocks. In 81 cases lymph node metastases were sampled in duplicate cores. In addition 1–3 cores from intestinal metaplasia (gastric intestinal metaplasia or Barrett’s esophagus) were sampled in 73 cases. Single core samples from adjacent normal gastric mucosa (131 cases) and normal squamous epithelium of the esophagus (96 cases) were also retrieved. All samples were paired.
For immunohistochemical analysis of IFITM1 expression, 4 μm TMA-sections were automatically pre-treated using the PT Link system and then stained in an Autostainer Plus (DAKO; Glostrup, Copenhagen, Denmark) with the rabbit polyclonal anti-IFITM1 antibody HPA004810 (Atlas Antibodies AB, Stockholm, Sweden) diluted 1:250. The specificity of the antibody has been validated . Staining was assessed by two different observers (DB and AG) blinded to clinical and outcome data. Scoring discrepancies were discussed to reach consensus. IFITM1 staining was mainly detected in the cytoplasm, with an accentuation towards the membrane. The fraction of stained tumor cells was scored as: 0 (0–1 %), 1 (2–25 %), 2 (26–50 %), 3 (51–75 %) or 4 (>75 %). Staining intensity was scored as: 0 (negative), 1 (weak), 2 (moderate) or 3 (strong). By multiplying fraction and intensity a combined score (0–12) was constructed.
Associations of IFITM1 expression in primary tumors with clinicopathological data
Entire cohort median (range)
Esophagus median (range)
GE junction median (range)
Stomach median (range)
Intestinal metaplasia background
Hazard ratios for recurrence and death M0 R0-1
Time to recurrence
HR (95 % CI)
HR (95 % CI)
HR (95 % CI)
HR (95 % CI)
Expression of IFITM1 in normal epithelium, intestinal metaplasia, primary tumors and lymph node metastases
Associations of IFITM1 expression in primary tumors with clinicopathological data
Table 2 describes the expression of IFITM1 in primary tumors in relationship to clinicopathological data for the entire cohort and for the separate tumor locations. In the entire cohort, IFITM1 was significantly elevated in M0-disease, most notably in gastric cancer. There was a trend towards higher IFITM1 expression in primary tumors with a background of intestinal metaplasia. In the subset of gastric tumors there were significant associations of high IFITM1 expression with age and Lauren’s intestinal type, respectively.
Impact of IFITM1 expression on survival
Of note, considering the association of high IFITM1 with Lauren’s intestinal type in gastric cancer (Table 2), we also tested to replace IFITM1 with Lauren classification in the adjusted Cox regression model but the hazard ratio of Lauren classification for TTR was not significant (data not shown) and when we added Lauren classification to the model with IFITM1 the hazard ratio of IFITM1 on TTR remained significant (data not shown). Thus, we do not believe that IFITM1 is just a marker for Lauren’s intestinal type.
Of the 78 patients that developed recurrent disease during the follow-up period, 36 patients received palliative treatment with chemotherapy and/or radiotherapy. To what extent palliative therapy may have affected the outcome is unclear, but due to a considerable heterogeneity regarding treatment type, doses and duration as well as to avoid selection bias (patients offered active palliative treatment usually have better performance status and prognosis) we decided not to include palliative oncological treatment after recurrence as a variable in the survival analyses.
The current study showed a significantly increased expression of IFITM1 in gastroesophageal adenocarcinoma compared to adjacent normal epithelium. This finding is in accordance with other reports on IFITM1 in gastric and colorectal adenocarcinoma [23, 34, 35]. The association of high IFITM1 expression and M0-disease, particularly seen in gastric cancer, has to our knowledge not been described previously.
In gastric cancer with high expression of IFITM1, we have demonstrated consistent findings of a beneficial effect on TTR. However, we could not demonstrate any significant relationship between IFITM1 and OS in gastric cancer, and one possible explanation for this could be the older age in these patients. It has previously been suggested that IFITM1 may have an adverse impact on OS in gastric cancer  but, even though our data on OS were non-significant, the association of elevated IFITM1 with M0-disease and the favorable impact on TTR implies that high expression of IFITM1 could rather be a positive prognostic factor in gastric cancer. It may seem like a paradox that the overexpression of IFITM1 in gastric cancer, which in other malignancies has been shown to promote tumorigenesis, was associated with M0-disease and a favorable TTR. A possible explanation might be that gastric tumorigenesis associated with elevated IFITM1 confers a less malignant phenotype. Support for this is the observed association of high IFITM1 expression and the prognostically favorable Lauren’s intestinal type demonstrated both in this study and by others . A similar contradiction has been described in glioma cells where knockdown of IFITM1 was demonstrated to inhibit proliferation, migration and invasion [17, 18], whereas reduced expression of IFITM1 correlated with shorter survival in a cohort of 30 glioma patients .
The proposed negative impact of IFITM1 on TTR and OS in esophageal adenocarcinoma has to be interpreted with caution since it was only demonstrated in the adjusted Cox regression analysis. However, if true, this would suggest the involvement of a different tumorigenic pathway than in gastric cancer. Esophageal and gastric cancers are indeed different malignancies, with diverging incidence trends and different risk factors. For instance, Helicobacter pylori infection is associated with gastric cancer  but may be a protective factor for esophageal cancer .
The exact function of IFITM1 in malignancy is poorly understood and its role might differ depending on tumor cell type and context. IFITM1 has been demonstrated to promote malignant progression in gastric cancer cells by increasing invasion and migration and by suppressing natural killer cell activity [23, 35]. It has been shown that IFITM1 expression is regulated by DNA methylation of its promoter region . Furthermore, expression of a transcript of CDH1 (E-cadherin) intron 2 (CDH1a) has been shown to increase gastric cancer cell invasion and angiogenesis and this increase correlated with IFITM1 expression . The downstream effectors of IFITM1 on tumorigenesis are largely unknown but one possible mechanism of promoting invasion could be the upregulation of matrix metalloproteinases .
An association between high IFITM1 expression and sensitivity to cisplatin has been described in esophageal squamous cell carcinoma  whereas in gastric cancer, overexpression of IFITM1 may confer resistance to cisplatin . Thus, future studies, on patient cohorts treated with neoadjuvant or palliative chemotherapy, would be of interest to further assess the possible role of IFITM1 as a predictive biomarker for response to platinum-based chemotherapy.
A limitation of our study is the retrospective design. However, all available surgically resected tumors were included consecutively, which decreases the risk of selection bias, and all clinical and histopathological data have been thoroughly re-examined. Another possible limitation is the use of the TMA technique, but since duplicate cores were obtained from different donor blocks, the risk of sampling bias should be low. Moreover, analyzing the data grouped by tumor location reduces the sample size and number of events and thus limits the possibility to adjust for multiple possible confounders in the Cox regression analyses. Due to the exploratory nature of the study, our results should mainly be regarded as hypothesis-generating, providing a basis for further exploration of IFITM1 as a biomarker in gastroesophageal adenocarcinoma.
In summary, we have shown that the immunohistochemical expression of IFITM1 was elevated in gastroesophageal adenocarcinoma and that it was associated with M0-disease. In gastric cancer, IFITM1 had a positive impact on TTR, whereas in esophageal cancer, data indicates an adverse impact on survival, suggesting that the role of IFITM1 may differ depending on the tumorigenic pathway. The mechanistic basis for this observation merits further study, and validatory studies on tumors from additional patient cohorts are warranted.
The study was approved by the regional ethics committee at Lund University (ref nr 445/07), whereby the committee waived the need for consent other than by the option to opt out.
interferon-inducible transmembrane protein 1
receiver operating characteristic
time to recurrence
This study was supported by grants from the Knut and Alice Wallenberg Foundation, the Swedish Cancer Society, the Crafoord Foundation, the Olle Engkvist Foundation, Anna Lisa and Sven-Eric Lundgren's Foundation, Lund University Faculty of Medicine and Skåne University Hospital Funds and Donations.
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