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首页> 外文期刊>Pathology International >Parp-1 deficiency in ES cells promotes invasive and metastatic lesions accompanying induction of trophoblast giant cells during tumorigenesis in uterine environment
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Parp-1 deficiency in ES cells promotes invasive and metastatic lesions accompanying induction of trophoblast giant cells during tumorigenesis in uterine environment

机译:ES细胞中Parp-1缺乏会促进子宫环境中肿瘤形成过程中伴随滋养层巨细胞诱导的侵袭性和转移性病变

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摘要

Embryonic stem (ES) cells deficient in poly(ADP-ribose) polymerase-1 (Parp-1) develop into teratocarcinomas with the appearance of trophoblast giant cells (TGCs) when injected subcutaneously into nude mice. Because the uterus is one of the original organs in which germ cell tumors develop with induction of trophoblast lineage, here we investigated whether Parp-1 deficiency in ES cells affects teratocarcinoma formation processes by grafting ES cells into the horns of uteri. Teratocarcinomas developed from both wild-type (Parp-1+/+) and Parp-1-/- ES cells. The weights of the tumors derived from Parp-1-/- ES cells were lower than those of the tumors derived from Parp-1+/+ ES cells (P0.05). The Parp-1-/- tumors showed the appearance of TGCs. Notably, organ metastasis to the lung and liver was observed for the Parp-1-/- tumors, but not for the Parp-1+/+ tumors (P 0.05). Invasions were more frequently observed with the Parp-1-/- tumors compared with the Parp-1+/+ tumors (P 0.05). Since TGCs are known to have invasive properties, the appearance of TGCs may have supported the metastatic process. The present findings suggest that loss of Parp-1 during teratocarcinoma formation might augment invasive and metastatic properties of the tumors in the uterine environment.
机译:缺乏聚(ADP-核糖)聚合酶-1(Parp-1)的胚胎干(ES)细胞皮下注射入裸鼠后,会发展为滋养层巨细胞(TGC)的畸胎癌。因为子宫是滋养细胞谱系诱导生殖细胞肿瘤发展的原始器官之一,所以在这里我们研究了ES细胞中Parp-1缺乏是否通过将ES细胞移植入子宫角而影响畸胎癌的形成过程。畸胎瘤由野生型(Parp-1 + / +)和Parp-1-/-ES细胞发展而来。来自Parp-1-/-ES细胞的肿瘤的重量低于来自Parp-1 + / + ES细胞的肿瘤的重量(P <0.05)。 Parp-1-/-肿瘤显示出TGC的出现。值得注意的是,对于Parp-1-/-肿瘤观察到了向肺和肝的器官转移,而对于Parp-1 + / +肿瘤则没有观察到(P <0.05)。与Parp-1 + / +肿瘤相比,Parp-1-/-肿瘤的侵袭率更高(P <0.05)。由于已知TGC具有侵袭性,因此TGC的出现可能支持了转移过程。目前的发现表明,畸胎癌形成过程中Parp-1的丢失可能会增强子宫环境中肿瘤的侵袭和转移特性。

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