Al-Saraireh Yousef M, Alboaisa Nafea S, Alrawashdeh Hamzeh Mohammad, Hamdan Omar, Al-Sarayreh Sameeh, Al-Shuneigat Jehad M, Nofal Mohammad N
Department of Pharmacology, Faculty of Medicine, University of Mutah, Karak 61710, Jordan.
Department of Pathology, College of Medicine, University of Anbar, Baghdad 55431, 55 Ramadi.
Ecancermedicalscience. 2020 Sep 29;14:1114. doi: 10.3332/ecancer.2020.1114. eCollection 2020.
Cytochromes P450 (CYPs) constitute an enzyme family involved in the oxidative metabolism of a wide variety of endogenous and exogenous compounds, including anti-cancer drugs and carcinogens. Unlike other human CYPs, CYP4Z1 is highly expressed in human breast carcinoma and is associated with poor prognosis. As a result, CYP4Z1 was hypothesised to be a potential biomarker or drug target for the discovery and development of promising anti-cancer therapies.
CYP4Z1 expression was immunohistochemically studied in a set of 100 different human tissues, including normal, benign, malignant and metastatic tissues, which originated from 27 anatomical sites. As a tumour model for CYP4Z1 expression, a panel of different breast cancers was evaluated for CYP4Z1 expression and its relation to histopathological features and prognostic immunohistochemical markers.
The immunohistochemical results revealed that CYP4Z1 was expressed in only one (4.3%) of the normal tissues from the mammary glands, while the expression of the enzyme was positive in 1 (11%), 12 (19%) and 2 (40%) of the benign, malignant and metastatic tissues, respectively. Interestingly, several tumour entities showed prominent expressions of CYP4Z1, including carcinomas of adrenal cortex, squamous cells of oesophagus, lung and cervix, as well as seminoma, astrocytoma, melanoma and lastly endometrial adenocarcinoma. In breast cancers, CYP4Z1 was expressed in 82% of the cases. Its expression was significantly associated with the pathology of tumour, histological grade and status of lymph node metastasis. Importantly, it was also significantly associated with the expressions of Her2, P53 and Ki-67.
These findings greatly support future plans for the use of CYP4Z1 as a biomarker or target for anti-cancer drugs. However, large-scale validation studies are needed to better delineate the potential use of CYP4Z1 for therapeutic purposes.
细胞色素P450(CYPs)构成一个酶家族,参与多种内源性和外源性化合物的氧化代谢,包括抗癌药物和致癌物。与其他人类CYPs不同,CYP4Z1在人类乳腺癌中高表达,且与预后不良相关。因此,推测CYP4Z1可能是发现和开发有前景的抗癌疗法的潜在生物标志物或药物靶点。
采用免疫组织化学方法研究了100种不同人类组织中CYP4Z1的表达,这些组织包括来自27个解剖部位的正常、良性、恶性和转移组织。作为CYP4Z1表达的肿瘤模型,评估了一组不同的乳腺癌中CYP4Z1的表达及其与组织病理学特征和预后免疫组化标志物的关系。
免疫组织化学结果显示,CYP4Z1仅在1例(4.3%)乳腺正常组织中表达,而该酶在良性、恶性和转移组织中的阳性表达率分别为1例(11%)、12例(19%)和2例(40%)。有趣的是,几种肿瘤实体显示出CYP4Z1的显著表达,包括肾上腺皮质癌、食管、肺和宫颈的鳞状细胞癌,以及精原细胞瘤、星形细胞瘤、黑色素瘤,最后是子宫内膜腺癌。在乳腺癌中,82%的病例表达CYP4Z1。其表达与肿瘤病理、组织学分级和淋巴结转移状态显著相关。重要的是,它还与Her2、P53和Ki-67的表达显著相关。
这些发现极大地支持了未来将CYP4Z1用作抗癌药物生物标志物或靶点的计划。然而,需要大规模的验证研究来更好地描绘CYP4Z1在治疗方面的潜在用途。