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J Cancer 2022; 13(3):869-876. doi:10.7150/jca.65145 This issue Cite

Research Paper

Low PARP-1 expression level is an indicator of poor prognosis in patients with stage II and III gastric cancer

Song Ee Park¹, Hee Sung Kim² , Eun-Jung Jung³, Ja Hee Suh³, Hyeyoung Min⁴, Kyong-Choun Chi⁵, Jong Won Kim⁵, Joong-Min Park⁵, In Gyu Hwang¹

1. Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
2. Department of Pathology, Chung-Ang University College of Medicine, Seoul, Korea.
3. Department of Pathology, National Medical Center, Seoul, Korea.
4. College of Pharmacy, Chung-Ang University, Seoul, Korea.
5. Department of Surgery, Chung-Ang University College of Medicine, Seoul, Korea.

✉ Corresponding authors: In Gyu Hwang, Division of Hemato-oncology, Department of Internal Medicine, Chung-Ang University College of Medicine, 84 Heukseok-ro, Dongjak-gu, Seoul 06973, Korea. Phone: +82-2-6299-1403; Fax:+82-2-6299-2114; E-mail: oncologyac.kr; Hee Sung Kim, Department of Pathology, Chung-Ang University College of Medicine, 84 Heukseok-ro, Dongjak-gu, Seoul 06973, Republic of Korea.Tel: 82-2-6299-3169; Fax: +82-2-6293-5630; E-mail: hkim1967ac.kr More

Abstract

Purpose: This study aimed to investigate the relationship between DNA damage response (DDR) related protein expression and clinical outcomes of patients with stage II and III gastric cancer undergoing gastrectomy.

Materials and Methods: From January 2005 to December 2017, 217 gastrectomized patients with stage II and III gastric cancer were analyzed for disease-free and overall survival (DFS and OS, respectively) based on their DDR expression status. We performed the immunohistochemical assessment of MLH1, MSH2, at-rich interaction domain 1 (ARID1A), poly adenosine diphosphate-ribose polymerase 1 (PARP-1), breast cancer susceptibility gene 1 (BRCA1), and ataxia-telangiectasia mutated (ATM) using formalin-fixed paraffin-embedded (FFPE) samples.

Results: Among the 217 patients studied, the most common DDR gene whose expression was suppressed was high PARP-1 (n = 120, 55.3%), followed by ATM (n = 62, 28.6%), ARID1A (n = 45, 20.7%), MLH1 (n = 33, 15.2%), BRCA1 (n = 25, 11.5%), and MSH2 (n = 9, 4.1%). The low-expression PARP-1 group exhibited a significantly shorter 5-year OS rate than the high-expression PARP-1 group (48.1% vs. 62.7%; HR 1.519, 95% CI = 1.011-2.283, P = 0.044). In the multivariate OS analysis, TNM stage (II vs. III) (HR = 5.172, P < 0.001), low PARP-1 expression (HR = 1.697, P = 0.013) and adjuvant chemotherapy (HR = 0.382, P < 0.001) were the only significant prognostic factors.

Conclusions: Low PARP-1 expression level could be an indicator of poor prognosis in gastrectomized patients with stage II and III gastric cancer.

Keywords: DNA damage response (DDR), Poly adenosine diphosphate-ribose polymerase 1 (PARP-1), Gastric cancer, Survival, Gastrectomy

Introduction

Gastric cancer is reportedly the fifth most common cancer and the third leading cause of cancer-related deaths worldwide [1]. At present, surgical resection and D1 or D2 gastrectomy are the main treatment approaches for stage II and III gastric cancer. However, even after curative resection, the 5-year survival rate is approximately 40-78% [2, 3]. Adjuvant chemotherapy is the standard treatment associated with resectable gastric cancer therapy; it has been reported to improve patient survival [3]. Adjuvant treatment reduces both distant and locoregional recurrences, although its related 5-year disease-free survival rate is poor (53-68%) [4]. However, despite its potential relevance, no clinically relevant survival- and post-surgical relapse-related prognostic marker for gastric cancer has been identified yet.

When DNA damage occurs, DNA damage response (DDR) is activated within a cell cycle checkpoint [5]. Defects in DDR could allow cell survival or the continuous growth of cancer cells [6]. DDR-related proteins, such as MLH1, MSH2 [7], AT-rich interaction domain 1A (ARID1A) [8], poly [ADP-ribose] polymerase 1 (PARP-1) [9], breast cancer susceptibility gene (BRCA1) [10], and ataxia-telangiectasia mutated protein (ATM) may allow cancer cells to evade physiological cell cycle checkpoints and facilitate cancer cell survival and proliferation.

DDR expression has been correlated with an improved response to cisplatin-based chemotherapy in urothelial cancer [11]. Genomic alterations in DNA response and repair-associated genes predicted responses and clinical benefits after cisplatin-based chemotherapy for bladder cancer. Low ATM expression levels were associated with poor overall 5-year survival in patients with gastric cancer undergoing curative surgical resection [12] and in patients with advanced gastric cancer undergoing palliative 1^st line XELOX therapy [13]. Recently, the phase III GOLD trial failed to show survival benefits in gastric cancer after first-line chemotherapy with olaparib [14].

Accordingly, it may be hypothesized that DDR-related protein defects are associated with poor survival in gastrectomized patients with stage II and III gastric cancer. Therefore, we investigated the relationship between the expression of DDR and gastric cancer patient survival to determine the survival-associated prognostic potential of DDR-related proteins.

Materials and Methods

Patients

A total of 217 patients with stage II and III primary gastric cancer were enrolled in this study, who had undergone D2 radical gastrectomy at the Chung-Ang University Hospital, between January 2005 and December 2017. The diagnosis of gastric cancer was confirmed by pathological staining. The cancer staging was performed according to the 7^th edition of the American Joint Committee on Cancer [15]. Patients with distant metastasis, such as liver metastasis, or peritoneal seeding were excluded. Adjuvant chemotherapy was the standard treatment for gastrectomized patients with stage II and III gastric cancer (unless the patient refused to undergo chemotherapy). This study was approved by the Institutional Review Board of Chung-Ang University Hospital (IRB number: 1981-005-382).

Immunohistochemistry

The immunohistochemical assessment of MLH1, MSH2, ARID1A, PARP-1, BRCA1, and ATM was performed using formalin-fixed paraffin-embedded (FFPE) tissue samples (Fig. S1).

The mismatch repair proteins MLH1 and MSH2 were scored based on the following threshold: positive when staining was detected in 10% or more of the tumor cell nuclei; negative when staining was detected in less than 10% of the tumor cell nuclei [16].

The PARP-1 staining was scored based on the staining intensity as follows: 0 (negative), 1 (weak), 2 (moderate), and 3 (strong). The percentage of staining distribution of each marker within the tumor cells was recorded. A histochemical (H) score was then calculated as follows: (1 percentage weak), (2 percentage moderate), and (3 percentage strong). The H-score is representative of the overall staining intensity ranges from 0 to 300 [17]. The PARP-1 staining was scored as follows: positive or high expression, staining achieving H-scores of more than 175; negative or low expression, staining achieving H-scores of less than 175.

The ARID1A staining was scored as follows: negative, undetectable; positive, no loss and focal loss [18]. The BRCA1 staining was scored as follows: negative, staining in less than 5% of the tumor cell nuclei; positive, staining in more than 5% of the tumor cell nuclei [19]. The ATM assay was evaluated based on the nuclear signal, with the percentage of weakly stained cells over a range of 0-300. A dichotomous classification system was devised whereby the cases were classified as follows: negative, intensity staining in ≤ 10% of the cancer cells (H-score ≤ 10) [20]; positive, staining in more than 10% of the cancer cells.

Assessment

Clinicopathological data, including patient age, sex, tumor-node-metastasis (TNM) stage, lymphatic invasion, venous invasion, perineural invasion, type of surgery, adjuvant chemotherapy, and chemotherapy regimen, were obtained retrospectively from medical records. The clinical outcomes included overall and disease-free survival (OS and DFS, respectively). OS was defined as the period between the gastrectomy and the time of death from any cause. DFS was defined as the period between the gastrectomy and the time of the recurrence of gastric cancer, distant metastasis, diagnosis of another cancer, or death from any cause.

Statistical analyses

Hazard ratios (HRs) and their corresponding 95% confidence intervals (CI) were stratified using a Cox proportional hazards regression model. Multivariate Cox regression models were constructed for testing significant variables based on the following criterion: P-value < 0.1 (for univariate analysis). The level of statistical significance was defined at P < 0.05. The Kaplan-Meier method was used to estimate the OS and DFS. All statistical analyses were performed using the Statistical Package for Social Sciences (SPSS) version 26.0 (IBM Corp., Armonk, NY, USA).

Results

Patients

The baseline characteristics of the patients are shown in Table 1. The median age was 67 years (ranging between 30-90) and 151 participants (69.6%), among the 217 patients studied in total, were men. The histological differentiation of the different cancer types was performed in the 217 patients. The depth of tumor invasion was evaluated as follows: 5.5% as T1 (n = 12, the tumor invades the mucosa or submucosa), 9.7% as T2 (n = 21, the tumor invades the muscularis propria), 47.0% as T3 (n = 102, the tumor invades the subserosal connective tissue without invading the visceral peritoneum or the adjacent structures), and 37.8% as T4 (n = 82, the tumor invades the serosa or the adjacent organs and structures). Lymph node metastasis was detected in 171 patients (78.8%), and 184 gastrectomized patients (84.8%) received adjuvant chemotherapy.

Expression of DDR-related proteins

Fig. 1 shows the relationship between the protein expression levels of MLH1, MSH2, ARID1A, PARP-1, BRCA1, and ATM and occurrence of gastric cancer. The most commonly mutated DDR expression was high PARP-1 (n = 120, 55.3%), followed by ATM (n = 62, 28.6%), ARID1A (n = 45, 20.7%), MLH1 (n = 33, 15.2%), BRCA1 (n = 25, 11.5%), and MSH2 (n = 9, 4.1%). Low PARP-1 expression levels did not depend on the following factors: an age of 65 years or older (P = 0.443) and sex (P = 0.692).

Association of PARP-1 and other DDR-related protein expressions with survival

The cutoff time for the analyses was January 2020, resulting in a median follow-up of 69.0 months (95% CI = 63.7-74.2 months) including the death of 95 patients (43.8%). The median OS and DFS were 89.0 months (95% CI = 81.1-100.3 months) and 60.0 months (95% CI = 25.0-94.9 months), respectively. One hundred and eight patients (49.8%) relapsed or died during the follow-up period. We evaluated the association between the expression of other DDR-related s MLH1, MSH2, ARID1A, BRCA1, and ATM and survival but observed no statistically significant difference.

The low-expression PARP-1 group exhibited a significantly shorter 5-year OS rate than the high-expression PARP-1 group (48.1% vs. 62.7%; HR 1.519, 95% CI = 1.011-2.283, P = 0.044). (Fig. 2A). Although these differences were not statistically significant, the low PARP-1 expression levels were marginally associated with a shorter median DFS, compared to the high PARP-1 expression levels (36.0 months vs. 96.0 months, HR 1.443, 95% CI = 0.998-2.109, P = 0.058) (Fig. 2B).

The univariate OS analysis of the potential prognostic impact of the clinicopathological parameters identified TNM stage, age, sex, lymph node metastasis, lymphatic invasion, perineural invasion, venous invasion, PARP-1, and adjuvant chemotherapy as significant predictors of OS (Table 2). In the multivariate OS analysis, TNM stage (II vs. III) (HR = 5.172, P < 0.001), low PARP-1 expression level (HR = 1.697, P = 0.013), and adjuvant chemotherapy (HR = 0.382, P < 0.001) were the only significant prognostic factors.

The univariate DFS analysis of the potential prognostic impact of the clinicopathological parameters identified TNM stage, age, sex, lymph node metastasis, lymphatic invasion, perineural invasion, venous invasion, and adjuvant chemotherapy as significant predictors of DFS (Table 3). In the multivariate DFS analysis, TNM stage (HR = 3.881, P < 0.001), low PARP-1 expression (HR = 1.547, P = 0.026), and adjuvant chemotherapy (HR = 0.596, P = 0.032) were found to be the only significantly prognostic factors.

 Figure 1 

Relationship between the expression levels of six DDR biomarkers (MLH1, MSH2, ARID1A, PARP-1, BRCA1, and ATM) (n = 217).

 Figure 2 

Low PARP-1 expression levels were associated with significantly shorter overall survival in patients with stage II and III gastric cancer (A). The disease-free survival was differentiated on the basis of PARP-1 expression (B).

Prognostic value of PARP-1 expression based on adjuvant chemotherapy

Of the patients with stage II and III gastric cancer who did not receive adjuvant chemotherapy, the low-expression PARP-1 group had significantly shorter median overall survival than the high-expression PARP-1 group (14.0 months vs. 49.0 months, HR = 2.659, 95% CI = 1.085-6.517, P = 0.032) (Fig. 3A). However, the 5-year overall survival rate in patients who had received adjuvant chemotherapy did not significantly differ between the low- and high-PARP-1 expression groups (59.2% vs. 64.9%, HR = 1.217, 95% CI = 0.760-1.949, P = 0.413) (Fig. 3B).

Impact of PARP-1 expression and other DDR-related protein expressions on adjuvant chemotherapy regimen

184 patients received adjuvant chemotherapy after gastrectomy. For 72 patients who received adjuvant oxaliplatin-based chemotherapy for resectable gastric cancer. The 5 year OS rate and 5 year DFS rate with adjuvant based chemotherapy for these 72 patients were 62.3% and 56.8%, respectively (Fig. 4). In low PARP-1 expression group, oxaliplatin based adjuvant chemotherapy group had not significantly different 5 year OS rate than no oxaliplatin based adjuvant chemotherapy group (63.9% vs. 54.9%, HR = 0.716, 95% CI= 0.331-1.547, P = 0.395) (Fig. 5A). In low PARP-1 expression group, oxaliplatin based adjuvant chemotherapy group had not significantly different DFS than no oxaliplatin based adjuvant chemotherapy group (74 months vs. 45 months, HR = 0.788, 95% CI= 0.389-1.594, P = 0.507) (Fig. 5B).

In low BRCA expression group, oxaliplatin based adjuvant chemotherapy group had not significantly different median 5 year OS than no oxaliplatin based adjuvant chemotherapy group (74.0 months vs. 43.0 months, HR = 0.993, 95% CI= 0.296-3.333, P = 0.992).

In low ATM expression group, oxaliplatin based adjuvant chemotherapy group had not significantly different 5 year OS rate than no oxaliplatin based adjuvant chemotherapy group (40.0% vs. 72.0%, HR = 2.414, 95% CI= 0.987-5.907, P = 0.054).

 Figure 3 

The overall survival of patients with stage II and III gastric cancer exhibiting high compared with those exhibiting low PARP-1 expression levels. Patients not having received (A) and having received adjuvant chemotherapy (B).

 Figure 4 

Overall survival (A) and disease free survival (B) according to oxaliplatin based adjuvant chemotherapy.

 Figure 5 

Overall survival (A) and disease free survival (B) according to oxaliplatin based adjuvant chemotherapy vs. no oxaliplatin based chemotherapy in low PARP-1 expression gastric cancer group.

Discussion

This study presented the results of the immunohistochemical assessment of the expression of DDR-protein in 271 patients with stage II and III gastric cancer. The results showed that low PARP-1 expression levels were associated with poor prognosis when gastrectomized patients underwent lymph node dissection. The low-expression PARP-1 group had significantly shorter median OS than the high-expression PARP-1 group in the case of patients with gastric cancer who did not receive adjuvant chemotherapy. However, the 5-year OS in patients who had received adjuvant chemotherapy did not significantly differ between the low- and high-expression PARP-1 groups.

In low expression PARP-1 patients, the prognosis of patients who received oxaliplatin based adjuvant chemotherapy was similar to the prognosis of patients who received no oxaplatin based adjuvant chemotherapy group. It suggested that the oxalipatin based adjuvant chemotherapy may not affect survival according to the low of PARP-1 expression. This study presented the clinical implication of DDR gene, but it should not find a correlation with clinical outcomes and other genes of DDR gene except of PARP-1 gene.

As reported in a previous study, the incidence of low PARP-1 expression was 47.2% in gastric cancer [21]; the incidence of low PARP-1 expression reported herein (44.7%) was similar to this value. Another study reported that the incidences of the loss of ATM, BRCA1, and ARID1A expression were 18-22 [13, 14], 17.5 [22], and 11-21% in gastric cancer [23], respectively. The expression of other DDRs were similar in our study. This study presented the clinical implications of the expression of DDR-related genes but did not highlight any correlation between clinical outcomes and the expression of other DDR-related genes (except PARP-1).

The PARP protein family comprises 17 enzymes involved in the regulation of the cell cycle, genome stability, transcription [24], DNA damage response [25], and cell death. High PARP-1 expression is associated with higher pathologically complete remission rates after neoadjuvant chemotherapy in breast cancer [26]. Inhibition of PARP-1 expression improves the efficacy of chemotherapy by impairing DNA repair [27]. These results provide the rationale behind the attempts to supplement chemotherapy with a PARP inhibitor in the presence of high PARP-1 expression levels.

PARP-1 expression is reportedly associated with a good prognosis in other cancer types, including breast cancer [28] and non-small-cell lung cancer [29]. Aiad et al [28] demonstrated that high PARP-1 expression levels were significantly associated with improved OS in locally advanced breast cancer. Klauschen et al [29] described that low PARP-1 expression levels were associated with a poor prognosis in pancreatic cancer. However, Liu et al [21] demonstrated that high PARP-1 expression levels were associated with significantly reduced DFS and OS in patients with gastric cancer. These studies indicate that PARP-1 expression could play different roles at different stages of tumors and treatments. In our study, low PARP-1 expression levels were associated with significantly poor DFS and OS in gastrectomized patients with stage II and stage III gastric cancer. According to our multivariate analysis, not only low PARP-1 expression levels, but also the TNM stage and adjuvant chemotherapy, were independent prognostic factors in gastric cancer.

Adjuvant chemotherapy after surgery in gastric cancer is a standard current treatment for stage II and III gastric cancer [3]. Patients who had received adjuvant chemotherapy showed similar OS rates irrespective of the PARP-1 expression levels. The prognostic effect was significant in the TNM stage and upon adjuvant chemotherapeutic treatment. Based on these observations, low PARP-1 expression levels may improve the efficacy of adjuvant chemotherapy when treating gastric cancer. Low PARP-1 expression levels could potentially favor the development of mutations through dysfunctional DNA repair, and PARP-1 could enhance the chemotherapeutic benefits with regard to survival. In gastric cancer, the high expression of PARP-1 may lead to the suppression of the activities of NAD+ and ATP, which in turn, may cause cell death [30].

The cytotoxic effects of platinum, including oxaliplatin, are to trigger a variety of downstream signaling pathways. High PARP-1 expression maybe affinity to the most common 1,2-d(GpG) and this affinity decreases upon automodification which implicates the role of PARP-1 in repair of platinum-induced DNA damage. Our data suggest that the low PARP-1 expression may have a role as predictive biomarkers for the response to adjuvant chemotherapy. However, the survival of oxalipatin based adjuvant chemotherapy was not better than the survival of no oxaliplatin based chemotherapy in patients with gastric cancer stage II or III. The 3 year DFS rate as 56% in our study with oxaliplatin base adjuvant chemotherapy was shorter than the 3 year DFS rate as 78% in the classic study[4]. In our study, the oxalipatin base adjuvant chemotherapy group was significantly more included stage III (P = 0.008), lymph node positive (P = 0.038), lymphatic invasion (P <0.001) and venous invasion (P = 0.005). The OS and DFS in the oxaliplatin base adjuvant chemotherapy group was worse because the factors that are not good for survival were included.

In conclusion, the present study demonstrated that low PARP-1 expression levels are associated with poor overall survival and disease-free survival. Low PARP-1 expression levels could be an indicator of poor prognosis, particularly in gastrectomized patients with stage II and III gastric cancer. Patients with stage II and stage III gastric cancer and low PARP-1 expression levels benefited from adjuvant chemotherapy. Therefore, adjuvant chemotherapy is required in patients with gastric cancer who display low PARP-1 expression levels.

Abbreviations

DDR: DNA damage response; DFS: disease-free survival; OS: overall survival; ARID1A: at-rich interaction domain 1; PARP-1: poly adenosine diphosphate-ribose polymerase 1; BRAC1: breast cancer susceptibility gene 1; ATM: ataxia-telangiectasia mutated; FFPE: formalin-fixed paraffin-embedded; HR: hazard ratio; CI: confidence interval.

Supplementary Material

Supplementary figure.

Acknowledgements

This study was supported by a grant from the National R&D Program for Cancer Control, Ministry of Health and Welfare, Republic of Korea (1720150).

The present study was supported by a National Research Foundation of Korea grant funded by the Korean government (grant no. 2014R1A1A2057925).

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding authors: In Gyu Hwang, Division of Hemato-oncology, Department of Internal Medicine, Chung-Ang University College of Medicine, 84 Heukseok-ro, Dongjak-gu, Seoul 06973, Korea. Phone: +82-2-6299-1403; Fax:+82-2-6299-2114; E-mail: oncologyac.kr; Hee Sung Kim, Department of Pathology, Chung-Ang University College of Medicine, 84 Heukseok-ro, Dongjak-gu, Seoul 06973, Republic of Korea.Tel: 82-2-6299-3169; Fax: +82-2-6293-5630; E-mail: hkim1967ac.kr

Received 2021-7-19
Accepted 2021-12-4
Published 2022-1-1

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