P16INK4A Expression on Retinoblastoma at Mohammad Hoesin Hospital Palembang

Sri Tanty Fuji A Harahap, Ika Kartika, Rusdianto
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Abstract

ABSTRACT Background: Retinoblastoma is a malignant tumor with an average incidence of one case per 15,000-20,000 births. Retinoblastoma is associated with the presence of the Rb1 gene mutation which has role in preventing DNA replication. Various studies have linked the existence of p16INK4A as a CDK inhibitor that inhibits Cyclin D and CDK4 so that the activity of the Rb1 gene is inhibited. Objective: This study was conducted to identify p16INK4A expression on Retinoblastoma at Mohammad Hoesin Hospital. Methodology: A descriptive study used on the paraffin blocks of 14 cases Retinoblastoma in Mohammad Hoesin Hospital Palembang from January 2014- July2018. Histopathologic feature were examined with Hematoxylin- Eosin staining and immunohistochemical were examined with p16INK4A antibody. Data were analyzed using SPSS version23 to identify histopathological feature of p16INK4A expression in Retinoblastoma Results: Most retinoblastoma samples in this study were expressed in p16INK4A (92.86%). The degree of differentiation of retinoblastoma with the largest number at Mohammad Hoesin Hospital is moderately differentiated (57.14%). Retinoblastoma invasion of the optic nerve and sclera in the study at Mohammad Hoesin Hospital, respectively at 57.14% and 42.86%. Conclusion: Most retinoblastoma samples in this study were expressed in p16INK4A.
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P16INK4A在Mohammad Hoesin医院视网膜母细胞瘤中的表达
背景:视网膜母细胞瘤是一种恶性肿瘤,平均发病率为1例/ 15000 - 20000例新生儿。视网膜母细胞瘤与Rb1基因突变的存在有关,Rb1基因突变在阻止DNA复制中起作用。各种研究已将p16INK4A的存在与CDK抑制剂联系起来,该抑制剂抑制Cyclin D和CDK4,从而抑制Rb1基因的活性。目的:研究p16INK4A在默罕默德·霍辛医院视网膜母细胞瘤组织中的表达。方法:对2014年1月至2018年7月在Palembang Mohammad Hoesin医院治疗的14例视网膜母细胞瘤的石蜡块进行描述性研究。采用苏木精-伊红染色检测组织病理特征,p16INK4A抗体检测免疫组化。采用SPSS version23对数据进行分析,确定p16INK4A在视网膜母细胞瘤中表达的组织病理学特征。结果:本研究中大多数视网膜母细胞瘤样本中表达p16INK4A(92.86%)。Mohammad Hoesin医院数量最多的视网膜母细胞瘤分化程度为中度分化(57.14%)。在Mohammad Hoesin医院的研究中,视网膜母细胞瘤侵袭视神经和巩膜的比例分别为57.14%和42.86%。结论:本研究中大多数视网膜母细胞瘤样本均表达p16INK4A。
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