Material and Method: DOG1 was evaluated in 100 cases of GISTs, immunohistochemically. Immunostaining index was counted for each antibody by using both the intensity and extent of staining. The association between immunostaining index of DOG1 and CD117, CD34, SMA desmin, S-100, and Ki-67 index and clinicopathological features were analyzed.
Results: Ninety cases were positive for DOG1, and 89 were positive for CD117. All CD117-negative tumors were positive for DOG1. High-risk group was directly correlated with tumor diameter, cellularity, necrosis, nuclear pleomorphism, mitotic count and Ki-67 index, by univariate analysis. The association between high-risk group and tumor diameter, mitotic count, and Ki-67 index was proved by multivariate analysis. Immunostaining index of DOG1, Ki-67 index, mitotic count, ulceration and hemorrhage were inversely correlated with overall survival by univariate analysis. The adverse impact of DOG1 ISI and mitotic count on overall survival were supported by multivariate analysis.
Conclusion: DOG1 positivity was detected in most of GISTs and all in CD117-negative cases as a result underlining its diagnostic utility. Additionally, DOG1 overexpression was related with adverse prognosis. Thus, we suggest that immunostaining index of DOG1 should routinely be used while diagnosing GIST, and DOG1 might be considered as a potential prognostic tool and a target for novel therapies.
DOG1 is a calcium-dependent chloride channel protein that is encoded by a gene called TMEM16A (TMEM16 FLJ10261, ANO1, ORAOV2, and AOS2) located on chromosome 11q13 [3]. DOG1 has many significant functions such as regulation of the cholinergic activity of gastrointestinal smooth muscle [4]-[6], and regulation of both the survival and proliferation of cells [7]. In addition DOG1 activates alternative signals downstream of the RAS/RAF/MEK/ERK and the insulin-like growth factor (IGF)- dependent pathways [4], [8]-[9]. These findings suggest that DOG1 may play a role in GIST development and progression, regardless of KIT and platelet-derived growth factor receptor alpha (PDGFRA) activation. DOG1 has been demonstrated to be positive in 89% of GISTs that have not CD117 or PDGFRA mutations [3]. In addition, DOG1 is claimed to be more sensitive and specific than CD117 in many studies, with some contradictory results in the literature [10]-[12]. About one third to one half of CD117- negative GISTs are reported to be positive for DOG1 [3]. Although the diagnostic utility of DOG1 for accurate GIST diagnosis is being widely investigated, its prognostic role is little evaluated in the literature. A few recent studies suggest that DOG1 expression affect the prognosis with some conflicting results [4], [10]-[15].
The goals of the present study were to review our archives in order to evaluate both the diagnostic and prognostic significance of DOG1 on GISTs, and achieve further data to clarify those issues in the current literature containing some contradictory results.
Statistical Analysis
All data were analyzed using PASW Statistics version 18.0 (SPSS Inc. Chicago. IL. USA). The demographic variables were detected using descriptive statistics. The compliance of data with normal distribution was evaluated with the Kolmogorov - Smirnov and Shapiro-Wilk tests. Independent Samples t-test (t test for independent groups) and One- Way ANOVA tests were used in order to investigate the quantitative data with normal distribution. Mann-Whitney U and Kruskal-Wallis H tests were used in the evaluation of the data that did not show normal distribution. The Tukey HSD test was applied in order to determine from which group the difference was originated. The Chi-squared test Fisher’s exact tests, Pearson and Spearman’s Rho correlation analysis were used for investigating the association between ISI’s of antibodies and the clinicopathological parameters. The effects of associated variables were studied by multiple linear regression analysis using backward method. P-value <0.05 was considered as significant.
We examined specimens from 100 patients (53 women and 47 men) with a mean age of 58.3}12.4 years (range 21 to 84). The tumors ranged from 0.4 to 25 cm (mean=6.06}4.24 cm) in diameter. Mitotic count varied from 0 to 80 (mean=7.4}15.3) per 50 high-power fields (HPFs). Four tumors were from esophagus, 60 tumors were from stomach, 7 were from duodenum, 11 were from jejunum 3 were from ileum, 3 were from colon, and 12 were from mesentery/omentum. According to the criteria of Fletcher et al., 70 (70%) cases were classified as lower-risk group (15 were very low-, 37 were low-, 18 were intermediate-risk group), and 30 (30%) cases as high-risk group. The followup time ranged from 1 to 94 months (mean=45.2}23.9 months). Thirteen of the 100 cases were deceased, and 87 cases were alive when the follow-up was finished. It was detected during follow-up that 2 cases died due to renal cell carcinomas, and the other 2 died due to colon adenocarcinomas, so those 4 cases were excluded from the survival analysis. Overall survival (OS) ranged from 1 to 94 months (mean=82.2}2.9 months). The clinicopathological features and their correlation with DOG1 expression of 100 GIST’s are summarized in Table I.
Table I: The clinicopathological features of GISTs (n: 100)
Immunohistochemical Findings
Ninety of 100 cases were positive for DOG1, 89 were positive for CD117, 77 were positive for CD34, 22 were positive for SMA, 10 were positive for desmin, and one was positive for S-100 .The detailed immunohistochemical findings underlining the correlation of DOG1 with other markers are given in Table II and Table III.
Table II: The correlations of DOG1 and other immunohistochemical markers (n: 100)
Table III: Immunostaining results of GISTs (n: 100)
All CD117-negative GISTs (11 cases) were positive for DOG1 (Figure 1A-C). Eight of them were positive for CD34, while 3 of them were negative for CD34. One of them was positive for SMA, while 10 of them were negative for SMA. All CD117-negative GISTs were negative for both desmin and S-100 . Male/female ratio in CD117-negative GISTs were 3/8. The mean age was 62.9}1.8 (range: 50- 83). Nine cases were in lower-risk group, 2 cases were in high-risk group. Nine tumors were from stomach, one was from sigmoid colon, and one was from mesentery. They were ranged from 0.4 to 11 cm in diameter. All of them had expansive growth pattern. Seven of them were composed of spindle cells, 3 were of epithelioid cells, and remaining one was of mixed (spindle+epithelioid) cells. Six showed mild cellularity, 3 showed moderate cellularity, and 2 showed high cellularity. Mild cellular atypia was present in 6 cases moderate cellular atypia was found in 2 cases, high cellular atypia was found in 2 cases, and no significant atypia was found in one case. Only one case showed ulceration. Hemorrhage was not present in any case. The mean mitotic count was 1.81}2.08 in 50 HPFs. Ki-67 proliferation index varied from 0% to 20% (mean=3.09}5.75%). Figure 1: Photomicrographs of a case of CD117-negative GIST. A) The tumor was composed of both epithelioid and spindle cells (H&E; x200). B) CD117 immunonegativity of the tumor cells (CD117; x200). C)Diffuse and strong immunopositivity of the tumor cells for DOG1 (DOG1; x200).
During follow-up, we detected that 3 of 10 DOG1 negative cases were deceased, while remaining 7 were alive. Ten of 90 DOG1 positive cases were found to be deceased. Six of those cases were deceased due to GISTs, 2 of those cases were deceased due to RCCs, and 2 of those were deceased due to colon carcinomas. Remaining 80 of DOG1 positive cases were found to be alive. There was no statistically significant correlation with DOG1 expression and current status of the patients (p=0.092). Mean OS was 52.4}33.2 months in DOG1 negative cases, while it was 44.5}22.8 in DOG1 positive cases. There was no statistically significant correlation between DOG1 positivity and OS (p=0.1). However, we detected that when ISI of DOG1 increased OS decreased, and that was statistically significant both by univariate (p=0.023) and multivariate analysis (p=0.006 β=-0.269, t=-2.819). The data about the mean OS of the cases according to the ISI of DOG1 is given in Table IV.
Table IV: The overall survival of cases according to ISI (immunostaining index) of DOG1
Sixty-seven cases showed <5 mitoses/50 HPFs with a mean OS of 48.1}24.3 months, while remaining 33 cases showed ≥5 mitoses/50 HPFs with a mean OS of 39.5}22.4 months. According to those data, OS was detected to be inversely correlated with mitotic count by both univariate (p=0.012) and multivariate analysis (p=0.003, β=-0.289 t=-3.032). Additionally, OS was found to be negatively correlated with Ki-67 proliferation index, ulceration and hemorrhage by univariate analysis (p=0.039, p=0.043 p=0.043, respectively), but those findings were not supported by univariate analysis. The results of univariate and multivariate analysis of clinicopathological and immunohistochemical features are summarized in Table V.
High-risk group was directly correlated with tumor diameter, cellularity, necrosis, cellular pleomorphism mitotic count and Ki-67 proliferation index (p=0.000 p=0.004, p=0.019, p=0.000, p=0.005, p=0.000, respectively) by univariate analysis. The association between highrisk group and tumor diameter, mitotic count and Ki-67 proliferation index was supported by multivariate analysis (p=0.000, each).
No statistically significant association was detected between expression of DOG1 and CD117, CD34, desmin, S-100 Ki-67 proliferation index, mitotic count, age, gender, risk group, tumor size, growth pattern, cellularity, nuclear pleomorphism, ulceration, hemorrhage, and necrosis (Table V).
Beside those immunohistochemical markers, performing Ki-67 is strongly recommended while diagnosing a GIST since high Ki-67 proliferation index is widely considered as an indicator of poor outcome in the literature [12,] [18]. Recently, some studies have suggested that Ki-67 proliferation index over than 10% indicates poor outcome [12], [21]-[24]. Similar to the literature, Ki-67 proliferation index more than 10% was found to be associated with low OS by univariate analysis in our study. We have also found a direct association with higher mitotic count and low OS and high-risk group by univariate analysis, similar to Ki- 67 labeling index. Nevertheless, we have demonstrated an inverse correlation between OS and higher mitotic count but not with Ki-67 proliferation index by multivariate analysis. This result might be contributed to the fact that mitotic count reflects the M phase of mitotic cycle, while Ki-67 indicates the proliferative cells in G1, S, and G2 phases [21]. Therefore, we think that higher mitotic count is still more reliable prognostic indicator than Ki-67 for GIST, and future studies should be conducted to clarify this issue.
Some recent studies have indicated that DOG1 might have potential prognostic affect in GIST [10], [12], [13], while some others have reported that it has only a diagnostic utility but not a prognostic value [25]. Sozutek et al. claimed that DOG1 negativity in GISTs may indicate poor prognosis however their result was not statistically significant [12]. Jung et al. have proposed that DOG1 negativity is significantly correlated with recurrence and/or metastasis [13]. However, Rizzo et al. have recently suggested that DOG1 overexpression might be used to predict poor prognosis of GISTs, since they have found low relapse-free survival in the cases with DOG1 overexpression than the cases with lower expression [4]. Similar to Rizzo et al., we have demonstrated an inverse correlation between OS and ISI of DOG1 by both univariate and multivariate analysis. In parallel to our and Rizzo et al.’s study [4], Li et al. [15] have documented that higher levels of DOG1 expression in peripheral blood mononuclear cells of GIST patients indicate poor prognosis and might be used for monitoring recurrence and investigating efficacy of imatinib therapy for GIST patients. In addition, DOG1 is known to intervene the receptor-activated chloride current and modulate the cell proliferation by influencing the retinoblastoma (Rb) tumor activating the MEK/ERK pathway [8]. Additionally xenograft DOG1-/- models of GISTs exhibit an impaired cell proliferation as a result of the reduced IGF binding protein-5 levels that inhibit IGF-mediated downstream signals by trapping both IGF1 and IGF2 [9], [26]. Thus, these data are likely that DOG1 overexpression might supply a proliferative advantage to malignant stromal cells, and elevated levels of DOG1 might adversely affect prognosis. However, we have not shown any association between ISI of DOG1 and Ki-67 proliferation index and mitotic count. That contradictory result might have been obtained due to other unknown signaling mechanisms related with DOG1 that should be clarified.
In the literature, there are some risk group classifications established for predicting the prognosis and malignant potential of GISTs [27]-[28]. In this study, we have used the risk assessment of Fletcher et al., due to its simplicity and widely use. Mitotic count, tumor size, anatomic location tumor necrosis, and nuclear pleomorphism have also been shown to be the prognostic parameters for GIST [27]-[29]. Similar to the literature, necrosis, high mitotic count, high cellularity, greater tumor size and high nuclear pleomorphism were also detected to be associated with high-risk group in the present study. Thus, we suggest that these features should be noted in the pathology reports as indicators of poor prognosis.
In summary, this study has showed that DOG1 is a reproducible and reliable marker for GIST diagnosis particularly for CD117-negative GISTs. We also strongly recommend that adding DOG1 in the routine immunohistochemical panel of GIST differential diagnosis (CD117, CD34, SMA, desmin, S-100) would aid establishment of accurate diagnosis of GIST. In addition, we have documented that DOG1 overexpression is related with poor outcome by both univariate and multivariate analysis. Thus, DOG1 ISI, referring the score of multiplication of staining intensity and extent, seems to be a useful prognostic tool as well as an ancillary diagnostic method. We claim that more comprehensive future studies including higher number of patients and longer follow-up might clarify the potential role of DOG1 on pathogenesis and prognosis of GISTs.
CONFLICT of INTEREST
The authors declare no conflict of interest.
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