Mohamed Amr M, Refaat Bassem A, El-Shemi Adel G, Kensara Osama A, Ahmad Jawwad, Idris Shakir
Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Umm Al-Qura UniversityMakkah, Kingdom of Saudi Arabia; Clinical Laboratory Diagnosis, Department of Animal Medicine, Faculty of Veterinary Medicine, Assiut UniversityAssiut, Egypt.
Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Umm Al-Qura University Makkah, Kingdom of Saudi Arabia.
Am J Transl Res. 2017 Feb 15;9(2):774-790. eCollection 2017.
Prevention of colon cancer among high-risk group has been long lasting research goal. Emerging data have evidenced the anticancer activities of Vitamin D3 (Vit.D) and Thymoquinone (TQ). The aim of the current study was to evaluate the synergistic potential of Thymoquinone and Vitamin D3 in the control of colon cancer progression using azoxymethane-induced rat model. Vit.D and TQ were given individually or in combination 4 week prior to induction and continued for a total of 20 week. At the end of the study, all animals were euthanized and their resected colons were examined macroscopically and microscopically for tumor growth. Colonic tissue preparations were used for measuring gene expression and/or protein levels of selected pro and anti-tumor biomarkers using quantitative RT-PCR, ELISA and immunohistochemistry. Compared with their individual supplementation, combined Vit.D/TQ showed prominent anti-tumor effect manifested by significant reduction (P < 0.05) of the numbers of grown tumors and large aberrant crypts foci. Mechanistically, gene expression and/or protein quantification studies revealed that combined Vit.D/TQ supplementation induced significant reduction (P < 0.01 and P < 0.05) of pro-cancerous molecules (Wnt, β-catenin, NF-κB, COX-2, iNOS, VEGF and HSP-90) as well as significant increase (P < 0.01 and P < 0.05, respectively) of anti-tumorigenesis biomarkers (DKK-1, CDNK-1A, TGF-β1, TGF-β/RII and smad4) as compared to un-supplemented or individually supplemented groups, respectively. In conclusion, TQ augmented the chemopreventive effect of Vit.D during the initiation phase of colon cancer in rat model, with the potential to suppress progression of pre-neoplastic lesions in colon carcinogenesis.
预防高危人群的结肠癌一直是长期的研究目标。新出现的数据证明了维生素D3(Vit.D)和百里醌(TQ)的抗癌活性。本研究的目的是使用氧化偶氮甲烷诱导的大鼠模型评估百里醌和维生素D3在控制结肠癌进展中的协同潜力。在诱导前4周单独或联合给予Vit.D和TQ,并持续共20周。在研究结束时,对所有动物实施安乐死,并对其切除的结肠进行宏观和微观检查以观察肿瘤生长情况。使用定量逆转录聚合酶链反应、酶联免疫吸附测定和免疫组织化学,对结肠组织标本进行检测,以测量所选促肿瘤和抗肿瘤生物标志物的基因表达和/或蛋白质水平。与单独补充相比,联合使用Vit.D/TQ显示出显著的抗肿瘤作用,表现为生长肿瘤数量和大的异常隐窝病灶显著减少(P<0.05)。从机制上讲,基因表达和/或蛋白质定量研究表明,与未补充或单独补充组相比,联合补充Vit.D/TQ可使致癌分子(Wnt、β-连环蛋白、核因子κB、环氧化酶-2、诱导型一氧化氮合酶、血管内皮生长因子和热休克蛋白90)显著减少(P<0.01和P<0.05),同时使抗肿瘤生物标志物(DKK-1、周期蛋白依赖性激酶抑制因子1A、转化生长因子-β1、转化生长因子-β受体II和Smad4)显著增加(分别为P<0.01和P<0.05)。总之,在大鼠结肠癌模型的起始阶段,TQ增强了Vit.D的化学预防作用,具有抑制结肠癌前病变进展的潜力。