Xanthatin nanocrystals exert anti-inflammatory properties against TNFα-primed 2D monolayers and in 3D spheroids of human HT29 colorectal cancer cells

IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Aleksandra Berenguer Roque, Alain Zgheib, Suslebys Salomon-Izquierdo, Amanda Manso Peña, Luis A. Osoria Alfonso, Janet Piloto-Ferrer, Borhane Annabi
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引用次数: 0

Abstract

Poor water-solubility of emerging new chemotherapeutic drugs lead to low absorption and tissue bioavailability. Improved drug delivery has therefore recently been achieved through the versatile physico-chemical properties of nanocrystals (NCs) in targeted cancer therapies. Here, nanocrystalization was used with xanthatin, a not highly water-soluble natural sesquiterpene lactone compound that possesses anti-tumour properties and which was recently investigated for potential use in the treatment of cancer and autoimmune diseases. Given that tumour-promoting inflammation is a hallmark of colorectal cancer (CRC), and that epidemiological studies associated inflammatory biomarkers to CRC poor prognosis and therapy resistance, the anti-inflammatory properties of xanthatin NCs were assessed in 2D monolayers and in 3D spheroids of a human HT29 CRC cell model. The 3D spheroids being a model recapitulating a cancer stem cells and chemoresistant phenotype. HT29 2D monolayer cell response was first tested against four pro-inflammatory inducers including phorbol-12-myristate-13-acetate, tumour necrosis factor alpha (TNFα), transforming growth factor beta, and Concanavalin A. Of these inducers, HT29 cell response to TNFα resulted in the most elevated expression of cyclooxygenase (COX)-2 which was prevented by commercial xanthatin along with the phosphorylation of the extracellular signal-regulated kinase 1/2 and of IkappaB (IκB). Alteration of 3D spheroids formation and of the inflammatory/immunity transcriptomic signature was also found better altered by xanthatin NCs in comparison to commercial xanthatin and the isolated molecule. Collectively, our data indicate that xanthatin nanocrystallization did not alter the potential in vitro anti-inflammatory and anticancer properties of xanthatin against a 3D CRC chemoresistance cellular model. These properties make NCs a significant advancement in the field of cancer theranostics to improve patient outcomes.

黄嘌呤纳米晶体对人HT29结直肠癌细胞tnf α-引发的二维单层和三维球体具有抗炎作用
新出现的化疗药物水溶性差,导致吸收和组织生物利用度低。因此,最近通过纳米晶体(NCs)在靶向癌症治疗中的多种物理化学特性,改善了药物输送。在这里,纳米结晶与黄嘌呤一起使用,黄嘌呤是一种不高度水溶性的天然倍半萜内酯化合物,具有抗肿瘤特性,最近被研究用于治疗癌症和自身免疫性疾病的潜在用途。鉴于促肿瘤炎症是结直肠癌(CRC)的标志,并且流行病学研究将炎症生物标志物与CRC预后不良和治疗耐药性联系起来,我们在人HT29 CRC细胞模型的2D单层和3D球体中评估了黄素NCs的抗炎特性。三维球体是一个模型概括癌症干细胞和化疗耐药表型。HT29 2D单层细胞对四种促炎诱诱剂(包括phorbol12 -肉豆酸酯-13-乙酸酯、肿瘤坏死因子α (TNFα)、转化生长因子β和豆豆蛋白a)的反应首先进行了测试。在这些诱诱剂中,HT29细胞对TNFα的反应导致环氧化酶(COX)-2的表达升高,这被商业黄素阻止,同时细胞外信号调节激酶1/2和IkappaB (IκB)磷酸化。与商业黄嘌呤和分离分子相比,黄嘌呤NCs更好地改变了3D球体形成和炎症/免疫转录组特征。总的来说,我们的数据表明,黄嘌呤纳米晶化并没有改变黄嘌呤在体外抗炎和抗癌的潜力,对三维结直肠癌化疗耐药细胞模型。这些特性使nc在癌症治疗领域取得了重大进展,改善了患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanoscale Research Letters
Nanoscale Research Letters 工程技术-材料科学:综合
CiteScore
11.30
自引率
0.00%
发文量
110
审稿时长
48 days
期刊介绍: Nanoscale Research Letters (NRL) provides an interdisciplinary forum for communication of scientific and technological advances in the creation and use of objects at the nanometer scale. NRL is the first nanotechnology journal from a major publisher to be published with Open Access.
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