Thani Noor Azela Abdullah, Keshavarz Sholeh, Lwaleed Bashir A, Cooper Alan J, Rooprai Harcharan K
School of Science and Technology, Middlesex University, The Burroughs, London, UK.
Faculty of Health Sciences, University of Southampton, Southampton, Hampshire, UK.
J Clin Pathol. 2014 Nov;67(11):949-54. doi: 10.1136/jclinpath-2013-202075. Epub 2014 Sep 17.
Extending work with brain tumours, the hypothesis that micronutrients may usefully augment anticancer regimens, chokeberry (Aronia melanocarpa) extract was tested to establish whether it has pro-apoptotic effects in AsPC-1, an established human pancreatic cell line, and whether it potentiates cytotoxicity in combination with gemcitabine. Pancreatic cancer was chosen as a target, as its prognosis remains dismal despite advances in therapy.
An MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) assay was used to assess the growth of the single pancreatic cancer cell line AsPC-1, alone and in comparison or combination with gemcitabine. This was backed up by flow cytometric DRAQ7 cell viability analysis. TUNEL assays were also carried out to investigate pro-apoptotic properties as responsible for the effects of chokeberry extract.
Chokeberry extract alone and its IC75 value (1 µg/mL) in combination with gemcitabine were used to assess the growth of the AsPC-1 cell line. Gemcitabine in combination with chokeberry extract was more effective than gemcitabine alone. TUNEL assays showed apoptosis to be a mechanism occurring at 1 µg/mL concentration of chokeberry, with apoptotic bodies detected by both colourimetric and fluorometric methods.
The implication of this study, using single cancer cell line, is that chemotherapy (at least with gemcitabine) might be usefully augmented with the use of micronutrients such as chokeberry extract.
在脑肿瘤研究的基础上进行拓展,鉴于微量营养素可能有效增强抗癌方案,对黑果腺肋花楸提取物进行了测试,以确定其在已建立的人胰腺癌细胞系AsPC-1中是否具有促凋亡作用,以及它与吉西他滨联合使用时是否能增强细胞毒性。选择胰腺癌作为研究对象,因为尽管治疗取得了进展,但其预后仍然很差。
采用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)法评估单一胰腺癌细胞系AsPC-1的生长情况,分别单独培养以及与吉西他滨进行比较或联合培养。流式细胞术DRAQ7细胞活力分析对此进行了补充验证。还进行了TUNEL检测,以研究促凋亡特性是否是黑果腺肋花楸提取物发挥作用的原因。
单独使用黑果腺肋花楸提取物及其与吉西他滨联合使用时的IC75值(1μg/mL)用于评估AsPC-1细胞系的生长情况。吉西他滨与黑果腺肋花楸提取物联合使用比单独使用吉西他滨更有效。TUNEL检测表明,在1μg/mL浓度的黑果腺肋花楸提取物作用下会发生凋亡,通过比色法和荧光法均检测到了凋亡小体。
本研究使用单一癌细胞系表明,化疗(至少使用吉西他滨时)可能通过使用黑果腺肋花楸提取物等微量营养素而得到有效增强。