Saad Eman A, Abd Allah Mona Y Y, Abd-El-Hameed Suzy Abd Elamabood, Abdel-Aziz Azza, Khaled Zalata
Department of Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Pediatric hematology, Oncology and Bone Marrow Transplantation Unit, Pediatrics Department, Professor of Pediatrics, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Asian Pac J Cancer Prev. 2025 Mar 1;26(3):1079-1087. doi: 10.31557/APJCP.2025.26.3.1079.
Chaperonin-Containing Tailless complex polypeptide 6A (CCT6A) is considered one of the biomarkers that play a role in cancer initiation, progression and resistance to body defenses and to anti-cancer drugs. Its exact prognostic role in Ewing sarcoma (ES) remains uncertain. The aim of this study is to assess immunohistochemical (IHC) expression of CCT6A in ES, and to assess the relation of its expression to different clinicopathological parameters and evaluate its prognostic significance in ES cases.
This retrospective cohort study included 35 cases diagnosed as ES at the Oncology Center of Mansoura University (OCMU), Faculty of Medicine, Egypt. Clinicopathological and survival data were collected. IHC for CCT6A was performed and correlated with clinicopathological parameters and patients' prognosis.
High IHC expression of CCT6A was found in 28 cases out of the studied 35 ES cases (80%), while 7 cases only (20%) showed low CCT6A expression. High CCT6A expression showed significant association with tumor size ≥8 cm (P= 0.01), treatment with adjuvant radiotherapy either for local control, infiltrated surgical margins or poor histopathological response to chemotherapy (P= 0.01), poor histopathological response to chemotherapy (P= 0.02), and HUVOS grades I and II (P= 0.01). High CCT6A expression was found to be a predictor of shorter overall survival and was an independent poor predictive factor by multivariate analysis (P= 0.03).
High CCT6A expression in ES associates with large tumor size, treatment with adjuvant radiotherapy for aforementioned indications, poor histopathological response to chemotherapy, and HUVOS grades I and II. Its high expression also independently predicts poor overall survival in ES patients. It may be used as a useful biomarker to predict prognosis of ES.
含伴侣蛋白的无尾复合多肽6A(CCT6A)被认为是在癌症发生、发展以及对机体防御和抗癌药物的抗性中发挥作用的生物标志物之一。其在尤因肉瘤(ES)中的确切预后作用仍不确定。本研究的目的是评估CCT6A在ES中的免疫组化(IHC)表达,并评估其表达与不同临床病理参数的关系,以及评估其在ES病例中的预后意义。
这项回顾性队列研究纳入了埃及曼苏拉大学医学院曼苏拉大学肿瘤中心(OCMU)诊断为ES的35例病例。收集临床病理和生存数据。进行CCT6A的IHC检测,并将其与临床病理参数和患者预后相关联。
在所研究的35例ES病例中,28例(80%)CCT6A的IHC高表达,而仅7例(20%)显示CCT6A低表达。CCT6A高表达与肿瘤大小≥8 cm(P = 0.01)、因局部控制、手术切缘浸润或化疗组织病理学反应差而接受辅助放疗(P = 0.01)、化疗组织病理学反应差(P = 0.02)以及HUVOS I级和II级(P = 0.01)显著相关。发现CCT6A高表达是总生存期较短的预测指标,并且通过多变量分析是独立的不良预测因素(P = 0.03)。
ES中CCT6A高表达与肿瘤体积大、因上述指征接受辅助放疗、化疗组织病理学反应差以及HUVOS I级和II级相关。其高表达还独立预测ES患者的总生存期差。它可能用作预测ES预后的有用生物标志物。