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食品级二氧化钛暴露会加剧结肠炎相关癌症模型中的肿瘤形成。

Food-grade titanium dioxide exposure exacerbates tumor formation in colitis associated cancer model.

作者信息

Urrutia-Ortega Ismael M, Garduño-Balderas Luis G, Delgado-Buenrostro Norma L, Freyre-Fonseca Verónica, Flores-Flores José O, González-Robles Arturo, Pedraza-Chaverri José, Hernández-Pando Rogelio, Rodríguez-Sosa Miriam, León-Cabrera Sonia, Terrazas Luis I, van Loveren Henk, Chirino Yolanda I

机构信息

Unidad de Biomedicina, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, CP 54059, Estado de México, Mexico; Programa de Doctorado en Ciencias Biomédicas, Universidad Nacional Autónoma de México, Mexico.

Unidad de Biomedicina, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, CP 54059, Estado de México, Mexico; Programa de Maestría en Ciencias Biológicas, Universidad Nacional Autónoma de México, Mexico.

出版信息

Food Chem Toxicol. 2016 Jul;93:20-31. doi: 10.1016/j.fct.2016.04.014. Epub 2016 Apr 23.

Abstract

Colorectal cancer is the fourth worldwide cause of death and even if some dietary habits are consider risk factors, the contribution of food additives including foodgrade titanium dioxide (TiO2), designated as E171, has been poorly investigated. We hypothesized that oral E171 intake could have impact on the enhancement of colorectal tumor formation and we aimed to investigate if E171 administration could enhance tumor formation in a colitis associated cancer (CAC) model. BALB/c male mice were grouped as follows: a) control, b) E171, c) CAC and d) CAC + E171 group (n = 6). E171 used in this study formed agglomerates of 300 nm in water. E171 intragastric administration (5 mg/kg body weight/5 days/10 weeks) was unable to induce tumor formation but dysplastic alterations were observed in the distal colon but enhanced the tumor formation in distal colon (CAC + E171 group) measured by tumor progression markers. Some E171 particles were internalized in colonic cells of the E171 and CAC + E171 groups and both groups showed a decrease in goblet cells in the distal colon. However the CAC + E171 group showed a higher decrease of these cells that act as protection barrier in colon. These results suggest that E171 could worsen pre-existent intestinal diseases.

摘要

结直肠癌是全球第四大致死原因,尽管一些饮食习惯被视为风险因素,但包括食品级二氧化钛(TiO₂,即E171)在内的食品添加剂的影响却鲜有研究。我们推测口服E171可能会促进结直肠癌的形成,旨在研究给予E171是否会在结肠炎相关癌症(CAC)模型中促进肿瘤形成。BALB/c雄性小鼠分为以下几组:a)对照组,b)E171组,c)CAC组和d)CAC + E171组(n = 6)。本研究中使用的E171在水中形成300纳米的团聚体。胃内给予E171(5毫克/千克体重/5天/10周)无法诱导肿瘤形成,但在远端结肠观察到发育异常改变,不过通过肿瘤进展标志物测量发现,其增强了远端结肠(CAC + E171组)的肿瘤形成。E171组和CAC + E171组的结肠细胞摄取了一些E171颗粒,两组远端结肠的杯状细胞均减少。然而,CAC + E171组这些作为结肠保护屏障的细胞减少得更多。这些结果表明,E171可能会使已有的肠道疾病恶化。

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