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Augmenting Therapy of Ovarian Cancer Efficacy by Secreting IL-21 Human Umbilical Cord Blood Stem Cells in Nude Mice

机译:通过在裸鼠中分泌IL-21人脐带血干细胞来增强卵巢癌疗效

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摘要

In the present study, CD34~+ human umbilical cord blood stem cells (UCBSCs) were engineered to express interleukin-21 (IL-21) and then were transplanted into A2780 ovarian cancer xenograft-bearing Balb/c nude mice. The therapeutic efficacy of this procedure on ovarian cancer was evaluated. The findings from the study indicated that UCBSCs did not form gross or histological teratomas until up to 70 days postinjection. The CD34~+ UCBSC-IL-21 therapy showed a consistent effect in the ovarian cancer of the treated mice, delaying the tumor appearance, reducing the tumor sizes, and extending life expectancy. The efficacy was attributable to keeping CD34~+ UCBSC-IL-21 in the neoplastic tissues for more than 21 days. The secreted IL-21 not only increased the quantity of CDlla~+ and CD56~+ NK cells but also increased NK cell cytotoxicit-ies to YAC-1 cells and A2780 cells, respectively. The efficacy was also associated with enhancing the levels of IFN-gamma, IL-4, and TNF-alpha in the mice as well as the high expressions of the NKG2D and MIC A/B molecules in the tumor tissues. This study suggested that transferring CD34~+ UCBSC-IL-21 into the nude mice was safe and feasible in ovarian cancer therapy, and that the method would be a promising new strategy for clinical treatment of ovarian cancer.
机译:在本研究中,将CD34〜+人脐带血干细胞(UCBSC)工程化以表达白介素21(IL-21),然后将其移植到A2780卵巢癌异种Balb / c裸鼠中。评价了该方法对卵巢癌的治疗效果。该研究的发现表明,UCBSC直到注射后长达70天才形成肉眼或组织畸胎瘤。 CD34〜+ UCBSC-IL-21治疗在治疗小鼠的卵巢癌中显示出一致的作用,延迟了肿瘤的出现,减小了肿瘤的大小,并延长了预期寿命。疗效归因于肿瘤组织中CD34〜+ UCBSC-IL-21的保留时间超过21天。分泌的IL-21不仅增加了CD11a +和CD56-+ NK细胞的数量,而且分别增加了NK细胞对YAC-1细胞和A2780细胞的细胞毒性。该功效还与提高小鼠中IFN-γ,IL-4和TNF-α的水平以及肿瘤组织中NKG2D和MIC A / B分子的高表达有关。这项研究表明,将CD34〜+ UCBSC-IL-21转移到裸鼠中是安全可行的,并且该方法将成为卵巢癌临床治疗的新策略。

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