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角质形成细胞生长因子-1对辐射诱导的唾液腺功能减退的辐射防护作用。

Radioprotective effects of Keratinocyte Growth Factor-1 against irradiation-induced salivary gland hypofunction.

作者信息

Choi Jeong-Seok, Shin Hyun-Soo, An Hye-Young, Kim Young-Mo, Lim Jae-Yol

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Incheon, Republic of Korea.

Translational Research Center, Incheon, Republic of Korea.

出版信息

Oncotarget. 2017 Feb 21;8(8):13496-13508. doi: 10.18632/oncotarget.14583.

Abstract

Irradiation can cause salivary gland hypofunction, with hyposalivation producing discomfort, health risks, and reducing function in daily life. Despite increasing translational research interest in radioprotection, there are no satisfactory treatments available. Keratinocyte growth factor-1 stimulates proliferation of salivary epithelial cells or salivary stem/progenitor cells. However, the exact mechanism of its radioprotection against radiation-induced salivary hypofunction is not fully elucidated. Our results reveal that the radioprotective effects of keratinocyte growth factor-1 involved alleviation of growth inhibition and anti-apoptotic cell death of human parotid epithelial cells. Furthermore, keratinocyte growth factor-1 protected human parotid epithelial cells through the phosphoinositide 3-kinase - protein kinase B (Akt) pathway and inhibition of p53-mediated apoptosis through activation of mouse double minute 2. Local delivery of keratinocyte growth factor-1 into the irradiated salivary glands could protect radiation-induced salivary cell damages, suppress p53-mediated apoptosis and prevent salivary hypofunction in vivo. This suggests that keratinocyte growth factor-1 is a promising candidate to prevent radiation-induced salivary hypofunction and raise rational development keratinocyte growth factor-1 local delivery system.

摘要

辐射可导致唾液腺功能减退,唾液分泌减少会产生不适、健康风险,并降低日常生活功能。尽管对辐射防护的转化研究兴趣日益增加,但目前尚无令人满意的治疗方法。角质形成细胞生长因子-1可刺激唾液上皮细胞或唾液干/祖细胞的增殖。然而,其对辐射诱导的唾液腺功能减退的辐射防护的确切机制尚未完全阐明。我们的研究结果表明,角质形成细胞生长因子-1的辐射防护作用包括减轻人腮腺上皮细胞的生长抑制和抗凋亡细胞死亡。此外,角质形成细胞生长因子-1通过磷酸肌醇3-激酶-蛋白激酶B(Akt)途径保护人腮腺上皮细胞,并通过激活小鼠双微体2抑制p53介导的细胞凋亡。将角质形成细胞生长因子-1局部递送至受辐射的唾液腺可保护辐射诱导的唾液细胞损伤,抑制p53介导的细胞凋亡,并在体内预防唾液腺功能减退。这表明角质形成细胞生长因子-1是预防辐射诱导的唾液腺功能减退的有前景的候选药物,并为角质形成细胞生长因子-1局部递送系统的合理开发提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/5355115/298f5870fc37/oncotarget-08-13496-g001.jpg

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