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ΔNp63调节人头颈部鳞状癌细胞的放射抗性。

ΔNp63 Regulates Radioresistance in Human Head and Neck Squamous Carcinoma Cells.

作者信息

Sato Kota, Yoshino Hironori, Sato Yoshiaki, Nakano Manabu, Tsuruga Eichi

机构信息

Department of Radiation Science, Graduate School of Health Sciences, Hirosaki University, Hirosaki 036-8564, Aomori, Japan.

Department of Bioscience and Laboratory Medicine, Hirosaki University Graduate School of Health Sciences, Hirosaki 036-8564, Aomori, Japan.

出版信息

Curr Issues Mol Biol. 2023 Jul 27;45(8):6262-6271. doi: 10.3390/cimb45080394.

Abstract

Radiation therapy is commonly used to treat head and neck squamous cell carcinoma (HNSCC); however, recurrence results from the development of radioresistant cancer cells. Therefore, it is necessary to identify the underlying mechanisms of radioresistance in HNSCC. Previously, we showed that the inhibition of karyopherin-β1 (KPNB1), a factor in the nuclear transport system, enhances radiation-induced cytotoxicity, specifically in HNSCC cells, and decreases the localization of SCC-specific transcription factor ΔNp63. This suggests that ΔNp63 may be a KPNB1-carrying nucleoprotein that regulates radioresistance in HNSCC. Here, we determined whether ΔNp63 is involved in the radioresistance of HNSCC cells. Cell survival was measured by a colony formation assay. Apoptosis was assessed by annexin V staining and cleaved caspase-3 expression. The results indicate that ΔNp63 knockdown decreased the survival of irradiated HNSCC cells, increased radiation-induced annexin V cells, and cleaved caspase-3 expression. These results show that ΔNp63 is involved in the radioresistance of HNSCC cells. We further investigated which specific karyopherin-α (KPNA) molecules, partners of KPNB1 for nuclear transport, are involved in nuclear ΔNp63 expression. The analysis of nuclear ΔNp63 protein expression suggests that KPNA1 is involved in nuclear ΔNp63 expression. Taken together, our results suggest that ΔNp63 is a KPNB1-carrying nucleoprotein that regulates radioresistance in HNSCC.

摘要

放射治疗常用于治疗头颈部鳞状细胞癌(HNSCC);然而,复发是由抗辐射癌细胞的发展导致的。因此,有必要确定HNSCC中抗辐射的潜在机制。此前,我们发现抑制核转运系统中的一种因子核转运蛋白-β1(KPNB1)可增强辐射诱导的细胞毒性,特别是在HNSCC细胞中,并减少SCC特异性转录因子ΔNp63的定位。这表明ΔNp63可能是一种携带KPNB1的核蛋白,可调节HNSCC中的抗辐射能力。在此,我们确定了ΔNp63是否参与HNSCC细胞的抗辐射能力。通过集落形成试验测量细胞存活率。通过膜联蛋白V染色和裂解的半胱天冬酶-3表达评估细胞凋亡。结果表明,ΔNp63敲低降低了受辐射HNSCC细胞的存活率,增加了辐射诱导的膜联蛋白V阳性细胞,并增加了裂解的半胱天冬酶-3表达。这些结果表明ΔNp63参与了HNSCC细胞的抗辐射能力。我们进一步研究了哪些特定的核转运蛋白-α(KPNA)分子,即KPNB1用于核转运的伴侣,参与核ΔNp63表达。对核ΔNp63蛋白表达的分析表明,KPNA1参与核ΔNp63表达。综上所述,我们的结果表明ΔNp63是一种携带KPNB1的核蛋白,可调节HNSCC中的抗辐射能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579f/10453785/41723dd92148/cimb-45-00394-g001.jpg

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