GADD45B as a Prognostic and Predictive Biomarker in Stage II Colorectal Cancer

Abstract

GADD45B acts as a member of the growth arrest DNA damage-inducible gene family, which has demonstrated to play critical roles in DNA damage repair, cell growth, and apoptosis. This study aimed to explore the potential relationship between GADD45B expression and tumor progression and evaluate the clinical value of GADD45B in stage II colorectal cancer (CRC). The expression patterns and prognostic value of GADD45B in CRC were analyzed based on The Cancer Genomic Atlas (TCGA). GADD45B expression features of 306 patients with stage II CRC and 201 patients with liver metastasis of CRC were investigated using immunochemical staining on tissue microarrays. Afterward, survival analysis and stratification analysis were performed in stage II to explore the prognostic and predictive significance of GADD45B. Overexpressed GADD45B is associated with poorer prognosis for CRC patients both in overall survival (OS) (p < 0.001) and disease-free survival (DFS) (p = 0.001) based on the TCGA database. Analysis results according to the stage II CRC cohort and the liver metastatic CRC cohort revealed that GADD45B was gradually upregulated in normal mucosa including primary colorectal cancer (PCC). Colorectal liver metastases (CLM) tissues were arranged in order (normal tissue vs. PCC p = 0.005 and PCC vs. CLM p = 0.001). The low GADD45B group had a significantly longer five-year OS (p = 0.001) and progression-free survival (PFS) (p < 0.001) than the high GADD45B group for the stage II patients. The multivariate Cox regression analysis results proved that the expression level of GADD45B was an independent prognostic factor for stage II after radical surgery (OS: Hazard Ratio (HR) 0.479, [95% confidence interval (CI) 0.305–0.753] and PFS:HR 0.490, [95% CI 0.336–0.714]). In high GADD45B expression subgroup of stage II cohort, the patients who underwent adjuvant chemotherapy had longer PFS than those who did not (p = 0.008). High expression levels of GADD45B is an independent prognostic factor of decreased OS and PFS in stage II CRC patients. The stage II CRC patients with high GADD45B expression might benefit from adjuvant chemotherapy.

1. Introduction

Colorectal cancer (CRC) is one of the most common cancers worldwide. Colorectal cancer is threatening public health. In China, CRC new cases and specific death estimates were approximately 191,000 and 376,300 annually, respectively [1]. On account of the prevalence of early CRC screening, the health outcomes of patients diagnosed with stage I or stage II CRCs has improved. However, the treatment options of early stage CRC, especially stage II, remains controversial. About 20% of the CRC patients who underwent curative surgery alone will develop systemic metastasis [2]. In addition, the previous study revealed that chemotherapy could improve survival of stage II CRC patients but absolute improvement in survival was less than 5% [3]. Furthermore, the adverse events of adjuvant chemotherapy have an impact on the quality of life of patients [4]. Therefore, it is essential to identify valuable biomarkers to stratify the tumor progression risk after surgery in stage II CRC. In this way, patients who were predicted to have metastasis might get a benefit from the chemotherapy. Conversely, low-risk patients could avoid the associated adverse effects and save themselves the cost of chemotherapy.

The GADD45 family, which consists of GADD45A (GADD45α, DDIT1), GADD45B (GADD45β, Myd118), and GADD45G (GADD45γ, cytokine-responsive 6, CR6), participates in many cellular processes associated with cell growth regulation and the stress signaling pathway [5]. The proteins encoded by the GADD45 gene family are small (18kDa), conservative, and have homology and high acidity [6]. GADD45B shares the common functions of the GADD45 family, which is associated with DNA damage repair, cell growth, apoptosis, and anti-tumor immune responses [7,8]. Meanwhile, GADD45B might play critical roles in the tumorigenesis of human embryonic carcinoma [9], hepatocellular carcinoma [10], and pituitary gonadotrope tumors [11]. GADD45β is related to NF-kB, which is known to influence tumorigenesis, cancer cell survival, apoptosis, invasion, and metastasis and the GADD45 family are essential mediators of cell survival in cancer cells with implications for cancer chemotherapy and novel drug discovery [9]. A recent study implicated the carcinogenesis function and potential prognostic value of GADD45B for CRC [12]. However, the role of GADD45B expression in the prognostic value and chemotherapy-related predictive significance in stage II CRC remains uncertain, which should gain more attention.

In the present study, we first evaluated the expression patterns of GADD45B in CRC and assessed prognostic significance based on The Cancer Genomic Atlas (TCGA). We further investigated the GADD45B expression features of stage II and liver metastatic CRC using immunochemical staining according to the data in our cohort. Lastly, survival analysis and stratification analysis were performed in stage II to explore the prognostic and predictive value of GADD45B.

2. Materials and Methods

2.1. Patients

The specimens in this study were collected from the patients who underwent the surgical resection between 2006 and 2012 at the Cancer Institute & Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College. All the diagnoses were confirmed according to the 7th edition American Journal of Critical Care (AJCC) TNM Classification. The inclusive criteria of stage II include the following: (A) AJCC pathology staging was stage II (T3-4N0M0); (B) no systemic or chemotherapy before the surgery; (C) the case can provide complete clinical information such as age, gender, tumor location, histology, differentiation, malignant tumors TNM classification, adjuvant therapy regime, follow-up information, and more. At the same time, we utilized the primary tumor and matched metastatic liver specimen to establish another simultaneous liver metastatic CRC (LMCRC) cohort. Totally, 306 cases of stage II CRC and 201 cases of simultaneous LMCRC were collected based on the inclusive criteria. All subjects gave their informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki, the Clinical Research Ethics Committee of Cancer Institute & Hospital, Chinese Academy of Medical Sciences approved this study (NCC2016JZ-06). All the patients were followed up every three months until 31 December 2017.

2.2. Genomic Analyses in the Public Dataset

To investigate the expression pattern and prognostic value of GADD45B, we analyzed colon cancer in 270 cases and rectal cancer in 92 cases provided by the TCGA project (Table S3). The Box Plots was generated to compare the GADD45B expression level between the tumor and normal tissues of CRC. The violin plots were created based on the patients’ pathological stages and GADD45B expression features. The Kaplan-Meier curves were plotted according to the expression value of GADD45B. The gene expression profiling interactive analysis (GEPIA) (http://gepia.cancer-pku.cn/index.html) is used for batch TCGA data processing and visualization in this study [13].

2.3. Tissue Microarray and Immunohistochemistry

The stage II tissue microarrays (TMAs) consisted of the tumor sample and matched normal tissue from each patient and LMCRC TMAs consisted of the primary colorectal cancer (PCC), colorectal liver metastases (CLM), normal intestinal mucosa, and normal liver tissue from each patient. All tumor tissue microarrays were built after being verified by hematoxylin and eosin (H&E) staining. The punched sample measured 1.0 mm and was obtained from the center of the tumor. All the tissue microarrays were assessed by using immunohistochemical (IHC) staining and an anti-GADD45B antibody (ab105060; 1:500; Abcam; Cambridge, UK). The IHC staining is referenced to immunohistochemistry protocols published by the Abcam Company online [14]. The expression of the TMAs was scored by two independent pathologists in a blind study, according to the Staining Index (SI) that was previously used to assess the expression pattern of GADD45B [15,16]. The SI score was calculated by multiplying the staining intensity (0, negative; 1, weak; 2, moderate; 3, strong) and the percentage of positive stained cells (no staining, 0; 1–10%, 1; 11–50%, 2; 50–100%, 3). In this study, a moderate/strong cytoplasm staining of (SI = 3–9) was defined as positive staining while a weak or negative staining (SI = 0–2) was defined as negative staining. Representative staining of GADD45B in the specimens was illustrated in Figure 1. The positive rate refers to the proportion of GADD45B positive staining samples especially positive rate = positive samples/ (positive samples + negative samples).

2.4. Statistical Analysis

The student’s t-test was used to compare the difference of the data between two groups. The Chi-square test or Fisher exact test was used to evaluate categorical data. Survival curves were plotted according to the Kaplan-Meier method and the log-rank test was used to compare the OS (overall survival), DFS (disease-free survival), and PFS (progression-free survival) in the study cohorts. Univariate and multivariate analysis for CRC prognosis were undertaken using the Cox proportional hazards regression model. The calculations were performed with International Business Machines (IBM) SPSS Statistics version 24.0 software program and R version 3.3.3. A value of p < 0.05 was considered significant.

3. Results

3.1. High GADD45B Expression Is Associated with Poorer Overall Survival and Disease-Free Survival in Colorectal Cancer Patients from the Public Database

We analyzed the GADD45B expression level of the CRC cases from the TCGA database and there was no significant difference between the PCC and normal tissues (NT) in both the colon cancer (COAD) and rectal cancer (READ) dataset (Figure 2A). Meanwhile, the average expression level of GADD45B turned out to have a rising trend as the development of the TNM pathology stage (Figure 2B). As shown in the Kaplan-Meier curves (Figure 2C,D), overexpressed GADD45B is associated with a poorer prognosis for CRC patients both in OS and DFS (p = 0.014 for OS; p = 0.041 for DFS).

3.2. The GADD45B Expression Pattern in Stage II Colorectal Cancer and Liver Metastatic Colorectal Cancer Cohort

To validate the results analyzed by the public database, we detected the expression patterns of GADD45B in the stage II CRC cohort and the LMCRC cohort. In these two cohorts, 306 cases of stage II CRC and 201 cases of simultaneous LMCRC included respectively. All the IHC staining results have been listed in

Table 1. The GADD45B expression pattern in different samples by immunohistochemical (IHC) staining.

	Sample	GADD45B-Positive	GADD45B-Negative	Positive Rate
Stage II	Tumor	132	174	43.14%
	Normal Tissue	113	193	36.93%
	Progression	60	51	50.45%
	Non-progression	72	123	38.97%
	Recurrence of Liver Metastasis after Surgery	19	12	61.29%
LMCRC	Primary Tumor	105	96	52.24%
	Normal Colorectal Mucosa	77	124	38.31%
	Liver Metastasis	137	64	68.16%
	Normal Liver Tissue	95	106	47.26%

Stage II: Stage II colorectal cancer, LMCRC: Liver metastatic colorectal cancer, Progression: Tumour recurrence after surgery in 5 years, Non-Progression: No recurrence signs after surgery in 5 years.

. In the stage II cohort, there was no significant difference regarding GADD45B protein expression in between the tumor tissue and the corresponding normal tissue (43.14% vs. 36.93%, p = 0.117). Based on the follow-up data, stage II was divided into the non-progression group (195 cases) and the progression group (111 cases) and 31 cases liver metastasis included in the latter group. Immunohistochemistry staining indicated that the progression group had a higher GADD45B expression positive rate than the non-progression group (50.45% vs. 38.97%, p = 0.004).

In the LMCRC cohort, GADD45B protein expression was detected in 105/201 (52.24%) of the PCC samples and 137/201 (68.16%) of the CLM samples (Table 1). At the same time, 77 cases (38.31%) of adjacent normal mucosa and 95 cases (47.26%) of the normal liver tissue showed staining-positive. Therefore, at protein levels, GADD45B was gradually upregulated in normal mucosa, PCC, and CLM tissues in order (normal tissue vs. PCC p = 0.005 and PCC vs. CLM p = 0.001).

We further compared the GADD45B expression of the primary tumor between stage II and LMCRC, and the results demonstrated that the latter was significantly upregulated (43.14% vs. 52.24%, p = 0.045). We also analyzed the GADD45B expression pattern in the primary tumor between stage II with liver metastasis after surgery and the simultaneous liver metastatic group. No significant difference was found (52.24% vs. 61.29%, p = 0.347).

3.3. The High GADD45B Expression Is Associated with Shorter Overall Survival and Progression-Free Survival in Stage II Colorectal Cancer

The association between the GADD45B expression of stage II primary and LMCRC patient pathologic characteristics is summarized in

Table 2. Correlation between the intensity of GADD45B expression and the clinical profiles of stage II colorectal cancer.

Factor	Total	GADD45B HIGH (%)	GADD45B LOW (%)	p Value
Age (years)
<65	216	89 (41.2)	127 (58.8)	0.290
≥65	90	43 (47.8)	47 (52.2)
Gender
Male	183	78 (42.6)	105 (57.4)	0.825
Female	123	54 (43.9)	69 (56.1)
Tumor Location
Colon	143	59 (72.4)	84 (27.6)	0.836
Rectum	163	73 (71.3)	90 (28.7)
Gross Pathological Type
Prominence	171	64 (41.3)	107 (58.7)	0.534
Ulceration & Infiltration	135	68 (44.8)	67 (55.2)
Grade
High	34	18 (52.9)	16 (47.1)	0.409
Middle	240	102 (42.5)	138 (57.5)
Low	32	12 (37.5)	20 (62.5)
T Stage
T3	286	125 (43.7)	161 (56.3)	0.175
T4	20	17 (56.7)	13 (43.3)
Adjuvant Therapy
Chemotherapy	131	53 (40.5)	78 (59.5)	0.377
Radiotherapy	63	32 (50.8)	31 (49.2)
No	112	47 (42.0)	65 (58.0)
Preoperative CEA Level(ng/mL)
≤5	244	101 (41.4)	143 (58.6)	0.222
>5	62	31 (50.0)	31 (50.0)
Preoperative CA19-9 Level(U/mL)
≤37	282	119 (42.2)	163 (57.8)	0.182
>37	23	13 (56.5)	10 (43.5)
MSI
MSS	268	120 (44.8)	148 (55.2)	0.124
MSI	38	12 (31.6)	26 (68.4)

CEA: Carcinoembryonic antigen; CA19-9: Carbohydrate antigen 19-9; MSI: Microsatellite instability; MSS: Microsatellite stable; T stage: Tumour stage.

. However, the clinicopathologic information such as age, gender, tumor location, gross pathology type, differentiation grade, T stage, preoperative carcinoembryonic antigen (CEA) level, preoperative carbohydrate antigen 19-9(CA19-9) level, and microsatellite instability (MSI) status had no significant correlation with the GADD45B expression.

To identify the prognosis value of GADD45B expression in CRC, the Kaplan Meier survival analyses were conducted in stage II. The median follow-up was more than 59 months and 78 cases of death, and 111 relapsed patients included. Kaplan Meier analysis revealed that in stage II patients, the low GADD45B group had a significantly longer five-year OS and PFS than the high GADD45B group (p = 0.001 for OS and p < 0.001 for PFS; Figure 3A,B).

3.4. GADD45B Expression Is an Independent Prognostic Factor in Stage II

Univariate Cox regression analysis confirmed that high GADD45B was associated with a worse prognosis significance for OS (HR 0.459, [95% CI 0.292–0.721]) and PFS (HR 0.480, [95% CI 0.330–0.699],

Table 3. Cox analyses of potential prognostic factors for overall survival in the stage II CRC cohort.

Factor	Comparison	Univariate Analysis			Multivariate Analysis
		HR	95% CI	p Value	HR	95% CI	p Value
MSI Status	MSI vs. MSS	0.343	0.126–0.939	0.037	0.379	0.138–1.039	0.059
GADD45B Expression	LOW vs. HIGH	0.459	0.292–0.721	0.001	0.479	0.305–0.753	0.001

HR: Hazard ratio; CI: confidence interval.

and

Table 4. Cox analyses of potential prognostic factors for progression-free survival in the stage II CRC cohort.

Factor	Comparison	Univariate Analysis			Multivariate Analysis
		HR	95% CI	p Value	HR	95% CI	p Value
Neurological Involvement	Present vs. Absent	2.222	1.191–4.145	0.012	2.066	1.107–3.858	0.023
GADD45B Expression	LOW vs. HIGH	0.480	0.330–0.699	0.0001	0.490	0.336–0.714	0.0002

, Tables S1 and S2). In the multivariate Cox regression analysis, high GADD45B expression was also significantly associated with the poorer rate of OS (HR 0.479, [95% CI 0.305–0.753]) and PFS (HR 0.490, [95% CI 0.336–0.714], Table 3 and Table 4, Tables S1 and S2). The results proved that low-level expression of GADD45B was an independent prognostic factor for stage II after radical surgery. Furthermore, neurological involvement was also a significant independent prognostic factor for PFS in the stage II cohort.

3.5. Expression of GADD45B Could Predict the Benefit from the Adjuvant Chemotherapy in Stage II Colorectal Cancer

Next, we investigated the potential role of GADD45B as a predictor of effectiveness of chemotherapy in stage II. In this cohort, 131 patients received the 5-Fluorouracil-based (5-FU-based) adjuvant chemotherapy, 63 lower rectal cancer patients underwent radiotherapy (50 gray (Gy)), and 112 patients didn’t take any adjuvant therapy after surgery. There appeared to be no significant difference in OS and PFS between the patients who received chemotherapy and the patients who never received the adjuvant treatment after surgery (p = 0.812 for OS and p = 0.257 for PFS; Figure 3C,D). To assess the predictive value of GADD45B for an adjuvant chemotherapy benefit, we compared the PFS of stage II CRC patients who underwent adjuvant chemotherapy or not in the subgroup after being stratified by GADD45B expression. In the high GADD45B expression subgroup, chemotherapy was associated with a higher rate of PFS (p = 0.008; Figure 3E), but this relationship did not exist in the subgroup of low GADD45B expression (p = 0.286, Figure 3F). The test of interaction results indicated that the benefit associated with adjuvant chemotherapy in the high GADD45B expression group was superior to the low GADD45B expression group (p = 0.027).

4. Discussion

In the present study, we evaluated the GADD45B expression pattern of different CRC development stages and prognostic values of GADD45B in stage II CRC. We first explored expression features of GADD45B in CRC based on the TCGA database and two CRC cohorts. As illustrated in the violin figure plotted by GEPIA, the expression level of GADD45B increased due to the development of the TNM stage. The results analyzed by our cohorts also indicated that the positive rate of GADD45B expression was rising in the primary tumor of stage II, PCC, and CLM of liver metastasis in order. Moreover, the IHC positive rate of GADD45B of the stage II progression group was higher than the non-progression group, but it turned out to have no significant difference in the primary tumor between stage II with liver metastasis after surgery and the simultaneous liver metastatic group. An associated study indicated that GADD45B contributed to tumor progression rather than the initiation in hepatocellular carcinoma and ovarian cancer [17]. Therefore, we infer that GADD45B may also be regarded as a potential tumor progression predictive marker in CRC.

When we made a survival analysis based on the TCGA data, the results suggested that the expression of GADD45B was significantly associated with the prognosis of CRC both in OS and PFS. Subsequently, the survival analysis was performed in the stage II cohort to validate the prognostic significance in this stage. It was shown that high expression of GADD45B was an independent prognostic factor of decreased OS and PFS accounting for stage II CRC. It was found that GADD45B had a predictive value to estimate the benefit from 5-FU-based chemotherapy in stage II. Additionally, in the previous studies, GADD45B was demonstrated to induce apoptosis and repair DNA damage in CRC cell lines, which plays a role in the tumor suppressor gene. This result seemed to be inconsistent with our study. However, a study published by Wang et al. [12] implicated that GADD45B might lose its normal functions and promote carcinogenesis and tumor progression in CRC tissues. At the same time, with the accumulation of DNA damage in tumor progression, the GADD45B expression level will improve feedback.

GADD45Beta is a stress-activated protein that plays a vital role in regulating apoptosis, proliferation, and DNA repair. It has been demonstrated to be an indicator for predicting clinical outcomes of gastric cancer [18], ovarian cancer [19], and glioma [20] according to the previous studies. Verzella et al. found that elevated GADD45B expression correlated with rapid disease progression in 13 of the top 15 solid cancers for mortality and the patient cohorts expressing high GADD45B levels exhibited significantly shorter recurrence-free survival and OS than the corresponding cohorts, which expressed low GADD45B messenger-RNA (mRNA) levels [16]. Even though a previous study has revealed the prognostic value of GADD45B in CRC, its validation cohort only included 152 cases with stage II–III [12]. Our study was performed to better understand the adjuvant chemotherapy indication-related problem for stage II patients with better clinical value. The results suggested that the benefit associated with adjuvant chemotherapy in the high GADD45B expression group was superior to the low GADD45B expression group. This result would provide stage II patients with a better selection for adjuvant chemotherapy to promote clinical outcomes and decrease overtreatment and cost. It was found that the stage II patients with low expression GAD45BB could appropriately change their chemotherapy regime or simply “look and wait.” Moreover, if we want to translate the finding into a better treatment strategy, more cohorts and larger size cases are needed and a related prospective study is also necessary.

This study has some limitations. First, our validation cohorts only consist of stage II and liver metastatic CRC patients and lack the other stages. Therefore, the next step should be to complete the CRC cohort establishment of stage I, stage III, and even precancerous stages to further vindicate the GADD45B expression characteristics in the development of CRC. In addition, all the cases in the cohort were collected from one single institution, which means further validations form multicenter and larger sample size cohorts are needed.

Currently, checkpoint inhibitor treatment is a major problem in tumor immunotherapy. Although immunotherapy has not been carried out in CRC widespread, it was shown that GADD45B could modulate innate immune checkpoint functions, which are amenable to therapeutic intervention to reprogram tumor-associated macrophages and ultimately overcome tumor microenvironments dependent on immunosuppression [17,21]. Moreover, as mentioned in the discussion above, inhibition of the GADD45B expression leads to suppression of proliferation and further prohibits tumor progression. Collectively, GADD45B is not only a prognostic factor in CRC but also a promising potential treatment target in the future.

5. Conclusions

The results suggest that a high expression level of GADD45B is an independent prognostic factor of decreased OS and PFS in stage II CRC patients. The stage II CRC patients with high GADD45B expression may benefit from adjuvant chemotherapy.