聚adp -核糖聚合酶-1 (PARP-1)表达与印尼巴厘岛鼻咽癌临床病理特征的关系

Putu Erika Paskarani, Ni Made Mahastuti, Silvia Https://sinta.ristekbrin.go.id/authors Khosasi, Made Dalika Nareswari
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From January 2018 to July 2022, biopsy tissue samples were collected from NPC patients, strictly following predefined inclusion and exclusion criteria. The clinical data of these patients were extracted from electronic medical records. Subsequently, the collected samples were subjected to immunohistochemical staining for PARP-1. The interpretation of PARP-1 results was conducted using the H-Score method. Data were analyzed using statistical software, specifically SPSS version 25.Results: The results showed that high PARP-1 expression was detected in 18 samples (62.1%), while the low aspect was observed in 11 samples (37.9%). Independent T-test analysis was conducted for sex, age, and clinical stage. No significant difference was found in the mean PARP-1 H-score among groups based on gender, age, and lymph node enlargement, with p-values of 0.68, 0.71, and 0.74, respectively. 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引用次数: 0

摘要

背景:根据巴厘岛开展的流行病学研究,鼻咽癌(NPC)是男性中最常见的癌症,占2017年至2019年报告病例总数的4.9%。鼻咽癌通常在IV期被发现,表明存在恶性细胞的远处转移。然而,关于poly - adp -核糖聚合酶-1 (PARP-1)在这类癌症中的作用的研究仍然有限。因此,本研究旨在探讨PARP-1与鼻咽癌临床病理方面的关系。方法:本研究采用横断面分析观察设计。2018年1月至2022年7月,严格按照预先确定的纳入和排除标准,从NPC患者中采集活检组织样本。这些患者的临床资料从电子病历中提取。随后,收集的样品进行PARP-1免疫组织化学染色。采用H-Score法解释PARP-1结果。数据分析使用统计软件,特别是SPSS版本25。结果:PARP-1高表达18例(62.1%),低表达11例(37.9%)。对性别、年龄、临床分期进行独立t检验分析。性别、年龄、淋巴结肿大组PARP-1 h -平均评分差异无统计学意义,p值分别为0.68、0.71、0.74。然而,PARP-1表达与临床分期有统计学意义(p=0.02, 95% CI 1.45 - 63.50)。多因素分析显示,性别、年龄、淋巴结肿大、临床分期占PARP-1表达变异的22.1%,与临床分期有显著相关性(p=0.02)。结论:鼻咽癌的临床病理资料显示男女比例为3:1。发现临床分期IVA和IVB是最常见的分期。PARP-1 h -评分在不同临床阶段的平均值和比例差异有统计学意义。未来的回顾需要包括其他组织学亚型,并采用前瞻性研究设计来评估PARP-1与NPC之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Relationship Between Poly-ADP-Ribose Polymerase-1 (PARP-1) Expression with Clinicopathological Characteristics of Nasopharyngeal Carcinoma in Bali, Indonesia
Background: According to epidemiological research conducted in Bali, nasopharyngeal carcinoma (NPC) is the most common cancer among males, accounting for 4.9% of total cases reported between 2017 and 2019. NPC is typically detected at stage IV, indicating the presence of distant metastasis by malignant cells. However, research on the role of Poly-ADP-Ribose Polymerase-1 (PARP-1) in this type of cancer is still limited. Therefore, this research aims to investigate the relationship between PARP-1 and the clinicopathological aspects of NPC.Methods: This research employed an analytical observational design with a cross-sectional approach. From January 2018 to July 2022, biopsy tissue samples were collected from NPC patients, strictly following predefined inclusion and exclusion criteria. The clinical data of these patients were extracted from electronic medical records. Subsequently, the collected samples were subjected to immunohistochemical staining for PARP-1. The interpretation of PARP-1 results was conducted using the H-Score method. Data were analyzed using statistical software, specifically SPSS version 25.Results: The results showed that high PARP-1 expression was detected in 18 samples (62.1%), while the low aspect was observed in 11 samples (37.9%). Independent T-test analysis was conducted for sex, age, and clinical stage. No significant difference was found in the mean PARP-1 H-score among groups based on gender, age, and lymph node enlargement, with p-values of 0.68, 0.71, and 0.74, respectively. However, a statistically significant association was found between PARP-1 expression and clinical stage (p=0.02, 95% CI 1.45 – 63.50). Multivariate analysis showed that sex, age, lymph node enlargement, and clinical stage accounted for 22.1% of the variation in PARP-1 expression, with the clinical stage demonstrating a significant correlation (p=0.02). Conclusions: The clinicopathological data of NPC indicate a male-to-female ratio of 3:1. It was discovered that clinical stages IVA and IVB were the most commonly observed stages. Statistically significant differences were found in the mean and proportion of PARP-1 H-scores across different clinical stages. Future reviews need to include other histological subtypes and employ a prospective research design to evaluate the relationship between PARP-1 and NPC.
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