Department of Pharmacology, Faculty of Medicine, Mutah University, P.O.Box 7, Karak, 61710, Jordan.
Department of Medical Lab Technology, Faculty of Health Sciences, The Public Authority for Applied Education and Training, P.O.Box 14281, 15432, Shuwaikh, Kuwait.
Sci Rep. 2021 Mar 10;11(1):5581. doi: 10.1038/s41598-021-85188-4.
Bladder cancer is the tenth most common cancer worldwide, where its burden remains a challenge and needs new novel therapies. Several reports indicate expression of CYP4Z1 and CYP1B1 in many tumours. Their expressions are associated with a poor prognosis, and therefore proposed as promising biomarkers or targets for anticancer therapy. By using immunohistochemistry, expression of CYP4Z1 and CYP1B1 was evaluated in a panel of different types of bladder cancer, and the enzymes' relation to histopathological features were assessed. Results showed an increased expression of CYP4Z1 (54.3%) and CYP1B1 (76.9%) in the majority of bladder cancers compared to weak or lack of expression of both enzymes in normal tissues. CYP4Z1expression was significantly associated with tumour grade and stage where the expression was markedly increased in a high grade and advanced stage of the disease (p < 0.05). Additionally, CYP1B1 expression was also associated with TNM staging (p < 0.05) and its expression was increased in patients with lymph node metastasis. The expression profiles of CYP4Z1 and CYP1B1 suggest that both enzymes have the potential to be biomarkers or targets for novel anticancer therapy for bladder cancer. Nevertheless, further studies are needed to better delineate whether these enzymes are druggable targets.
膀胱癌是全球第十大常见癌症,其负担仍然是一个挑战,需要新的治疗方法。有几项报告表明 CYP4Z1 和 CYP1B1 在许多肿瘤中表达。它们的表达与预后不良有关,因此被提议作为有前途的生物标志物或抗癌治疗靶点。本研究通过免疫组织化学方法,在一系列不同类型的膀胱癌中评估了 CYP4Z1 和 CYP1B1 的表达,并评估了这些酶与组织病理学特征的关系。结果显示,与正常组织中两种酶的弱表达或缺乏表达相比,大多数膀胱癌中 CYP4Z1(54.3%)和 CYP1B1(76.9%)的表达增加。CYP4Z1 表达与肿瘤分级和分期显著相关,在疾病的高级别和晚期表达明显增加(p<0.05)。此外,CYP1B1 表达也与 TNM 分期相关(p<0.05),在有淋巴结转移的患者中表达增加。CYP4Z1 和 CYP1B1 的表达谱表明,这两种酶都有可能成为膀胱癌新的抗癌治疗的生物标志物或靶点。然而,需要进一步的研究来更好地阐明这些酶是否是可用药的靶点。