Messina Concetta Maria, Pizzo Federica, Santulli Andrea, Bušelić Ivana, Boban Mate, Orhanović Stjepan, Mladineo Ivona
Dipartimento di Scienze della Terra e del Mare DiSTeM, Università degli Studi di Palermo, Laboratorio di Biochimica Marina ed Ecotossicologia, Via G. Barlotta 4, 91100, Trapani, Italy.
Institute of Oceanography and Fisheries, Laboratory of Aquaculture, POBox 500, 21000, Split, Croatia.
Parasit Vectors. 2016 Nov 25;9(1):607. doi: 10.1186/s13071-016-1895-5.
In countries with elevated prevalence of zoonotic anisakiasis and high awareness of this parasitosis, a considerable number of cases that associate Anisakis sp. (Nematoda, Anisakidae) and different bowel carcinomas have been described. Although neoplasia and embedded larvae were observed sharing the common site affected by chronic inflammation, no association between the nematode and malignancy were directly proved. Similarly, no data are available about the effect of secretory and excretory products of infecting larvae at the host's cellular level, except in respect to allergenic interaction.
To test the mechanisms by which human non-immune cells respond to the larvae, we exposed the fibroblast cell line HS-68 to two Anisakis products (ES, excretory/secretory products; and EC, crude extract) and evaluated molecular markers related to stress response, oxidative stress, inflammation and apoptosis, such as p53, HSP70, TNF-α, c-jun and c-fos, employing cell viability assay, spectrophotometry, immunoblotting and qPCR.
Both Anisakis products led to increased production of reactive oxygen species (ROS), especially in EC-treated cells. While the ES treatment induces activation of kinases suggesting inflammation and cell proliferation (or inhibition of apoptosis), in EC-treated cells, other signaling pathways indicate the inhibition of apoptosis, marked by strong upregulation of Hsp70. Elevated induction of p53 in fibroblasts treated by both Anisakis products, suggests a significantly negative effect on the host DNA.
This study shows that in vitro cell response to Anisakis products can result in at least two different scenarios, which in both cases lead to inflammation and DNA damage. Although these preliminary results are far from proving a relationship between the parasite and cancer, they are the first to support the existence of conditions where such changes are feasible.
在人兽共患异尖线虫病患病率较高且对这种寄生虫病认知度较高的国家,已经描述了相当数量的将异尖线虫属(线虫纲,异尖科)与不同类型肠癌相关联的病例。尽管观察到肿瘤形成和包埋的幼虫存在于受慢性炎症影响的共同部位,但线虫与恶性肿瘤之间的关联尚未得到直接证实。同样,除了关于过敏相互作用方面,关于感染幼虫的分泌和排泄产物在宿主细胞水平上的影响尚无数据。
为了测试人类非免疫细胞对线虫幼虫的反应机制,我们将成纤维细胞系HS - 68暴露于两种异尖线虫产物(ES,排泄/分泌产物;以及EC,粗提物),并通过细胞活力测定、分光光度法、免疫印迹和定量聚合酶链反应评估与应激反应、氧化应激、炎症和凋亡相关的分子标志物,如p53、热休克蛋白70(HSP70)、肿瘤坏死因子-α(TNF-α)、c - jun和c - fos。
两种异尖线虫产物均导致活性氧(ROS)生成增加,尤其是在经EC处理的细胞中。虽然ES处理诱导激酶激活,提示炎症和细胞增殖(或凋亡抑制),但在经EC处理的细胞中,其他信号通路表明凋亡受到抑制,其标志是Hsp70的强烈上调。两种异尖线虫产物处理的成纤维细胞中p53的诱导升高,表明对宿主DNA有显著的负面影响。
本研究表明,体外细胞对异尖线虫产物的反应可导致至少两种不同情况,在这两种情况下均会导致炎症和DNA损伤。尽管这些初步结果远未证明寄生虫与癌症之间的关系,但它们首次支持了存在这种变化可行的条件。