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12-O-十四烷酰佛波醇-13-乙酸酯(TPA)可提高辐射损伤后小鼠肠道隐窝干细胞的存活率。

12-O-tetradecanoylphorbol-13-acetate (TPA) increases murine intestinal crypt stem cell survival following radiation injury.

作者信息

Liang Yaojie, Zhou Hongwei, Yao Yibing, Deng Ailing, Wang Zhihong, Gao Boning, Zhou Minhang, Cui Yu, Wang Lili, Zhou Lei, Wang Bianhong, Wang Li, Liu Anqi, Qiu Lanlan, Qian Kun, Lu Yejian, Deng Wanping, Zheng Xi, Han Zhengtao, Li Yonghui, Sun Junzhong

机构信息

Department of Geriatric Oncology, The First Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.

Department of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Oncotarget. 2017 Jul 11;8(28):45566-45576. doi: 10.18632/oncotarget.17269.

Abstract

Radiation enteropathy is a common complication in cancer patients following radiation therapy. Thus, there is a need for agents that can protect the intestinal epithelium against radiation. 12-O-tetradecanoylphorbol-13-acetate (TPA) has been shown to induce differentiation and/or apoptosis in multiple cell lines and primary cells. In the current report, we studied the function of TPA in radiation induced enteropathy in cultured rat intestinal epithelial cell line IEC-6 after ionizing radiation (IR) and in mice after high dose total-body gamma-IR (TBI). In IEC-6 cells, there were reduced apoptosis and cell cycle arrest in TPA treated cells after IR. We detected a four-fold increase in crypt cell survival and a two-fold increase in animal survival post TBI in TPA treated mice. The beneficial effects of TPA were accompanied by upregulation of stem cells markers and higher level of proteins that are involved in PKC signaling pathway. In addition, TPA also decreased the TBI-augmented levels of the DNA damage indicators. The effects were only observed when TPA was given before irradiation. These results suggest that TPA has the ability to modulate intestinal crypt stem cells survival and this may represent a promising countermeasure against radiation induced enteropathy.

摘要

放射性肠病是癌症患者放疗后的常见并发症。因此,需要能够保护肠上皮免受辐射的药物。12-O-十四烷酰佛波醇-13-乙酸酯(TPA)已被证明可诱导多种细胞系和原代细胞的分化和/或凋亡。在本报告中,我们研究了TPA在电离辐射(IR)后对培养的大鼠肠上皮细胞系IEC-6以及高剂量全身γ-IR(TBI)后对小鼠放射性肠病的作用。在IEC-6细胞中,IR后TPA处理的细胞凋亡减少且细胞周期停滞。我们检测到TPA处理的小鼠在TBI后隐窝细胞存活率增加四倍,动物存活率增加两倍。TPA的有益作用伴随着干细胞标志物的上调以及参与PKC信号通路的蛋白质水平升高。此外,TPA还降低了TBI增强的DNA损伤指标水平。仅在照射前给予TPA时才观察到这些效果。这些结果表明TPA具有调节肠隐窝干细胞存活的能力,这可能是对抗放射性肠病的一种有前景的对策。

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