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首页> 外文期刊>Cancer research: The official organ of the American Association for Cancer Research, Inc >Clld7, a candidate tumor suppressor on chromosome 13q14, regulates pathways of DNA damage/repair and apoptosis.
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Clld7, a candidate tumor suppressor on chromosome 13q14, regulates pathways of DNA damage/repair and apoptosis.

机译:Clld7,染色体13℃的候选肿瘤抑制剂,调节DNA损伤/修复和细胞凋亡的途径。

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摘要

Chronic lymphocytic leukemia deletion gene 7 (Clld7) is a candidate tumor suppressor on chromosome 13q14. Clld7 encodes an evolutionarily conserved protein that contains an RCC1 domain plus broad complex, tramtrack, bric-a-brac (BTB), and POZ domains. In this study, we investigated the biological functions of Clld7 protein in inducible osteosarcoma cell lines. Clld7 induction inhibited cell growth, decreased cell viability, and increased gamma-H2AX staining under conditions of caspase inhibition, indicating activation of the DNA damage/repair pathway. Real-time PCR analysis in tumor cells and normal human epithelial cells revealed Clld7 target genes that regulate DNA repair responses. Furthermore, depletion of Clld7 in normal human epithelial cells conferred resistance to apoptosis triggered by DNA damage. Taken together, the biological actions of Clld7 are consistent with those of a tumor suppressor.
机译:慢性淋巴细胞白血病缺失基因7(CLLD7)是染色体13Q14上的候选肿瘤抑制剂。 CLLD7编码一种进化保守的蛋白质,包含RCC1域加上宽复杂,轨道,BRIC-A-BRAC(BTB)和POZ结构域。 在这项研究中,我们研究了Clld7蛋白在诱导骨肉瘤细胞系中的生物学功能。 Clld7诱导抑制细胞生长,细胞生长,降低细胞活力,并在胱天蛋白酶抑制条件下增加γ-H2AX染色,表明DNA损伤/修复途径的激活。 肿瘤细胞的实时PCR分析和正常人上皮细胞揭示了调节DNA修复反应的Clld7靶基因。 此外,在正常人上皮细胞中Clld7的耗尽赋予DNA损伤引发的凋亡。 连同,CLLD7的生物学作用与肿瘤抑制剂的生物学作用一致。

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