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Conditional Tnfaip6‑Knockout in Inner Ear Hair Cells Does not Alter Auditory Function
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作者 Yue Qiu Song Gao +9 位作者 Xiaoqiong Ding Jie Lu Xinya Ji Wenli Hao Siqi Cheng Haolinag Du Yajun Gu Chenjie Yu Cheng Cheng Xia Gao 《Neuroscience Bulletin》 2025年第3期421-433,共13页
Noise-induced hearing loss is a worldwide public health issue that is characterized by temporary or permanent changes in hearing sensitivity.This condition is closely linked to inflammatory responses,and interventions... Noise-induced hearing loss is a worldwide public health issue that is characterized by temporary or permanent changes in hearing sensitivity.This condition is closely linked to inflammatory responses,and interventions targeting the inflammatory gene tumor necrosis factoralpha(TNFα)are known to mitigate cochlear noise damage.TNFα-induced proteins(TNFAIPs)are a family of translucent acidic proteins,and TNFAIP6 has a notable association with inflammatory responses.To date,there have been few reports on TNFAIP6 levels in the inner ear.To elucidate the precise mechanism,we generated transgenic mouse models with conditional knockout of Tnfaip6(Tnfaip6 cKO).Evaluation of hair cell morphology and function revealed no significant differences in hair cell numbers or ribbon synapses between Tnfaip6 cKO and wild-type mice.Moreover,there were no notable variations in hair cell numbers or hearing function in noisy environments.Our results indicate that Tnfaip6 does not have a substantial impact on the auditory system. 展开更多
关键词 Noise tnfaip6 Hair cells Hearing loss
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Role of tumor necrosis factor alpha-induced protein 6(TNFAIP6)in tumors:a pan-cancer analysis
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作者 Yang Yang Zhi-Gang Liu +4 位作者 Yan-Qi Yang Zhi-Gang Zhang Xiao-Li Wang Yu-Long Li Rui-Fang Sun 《Oncology and Translational Medicine》 2024年第1期22-29,共8页
Background:There is growing evidence that the gene named tumor necrosis factorα–induced protein 6(TNFAIP6)has an important role in various tumors.However,a systematic pan-cancer analysis of TNFAIP6 is lacking.Here w... Background:There is growing evidence that the gene named tumor necrosis factorα–induced protein 6(TNFAIP6)has an important role in various tumors.However,a systematic pan-cancer analysis of TNFAIP6 is lacking.Here we aimed to analyze the expression of TNFAIP6 across multiple cancers and verify its expression during the progression of colon cancer.Methods:We performed a comprehensive bioinformatics analysis to examine the expression of TNFAIP6 across 27 tumor types.GEPIA2 was used to evaluate the effect of TNFAIP6 on clinical cancer prognosis.cBioportal was used to assess TNFAIP6 mutations.The correlation between TNFAIP6 and cancer immune infiltrates was explored using TIMER2.0.The CancerSEA database was used to perform functional analysis of TNFAIP6.Metascape was used to identify TNFAIP6-related gene enrichment pathways.Immunohistochemistry was performed to detect TNFAIP6 protein expression in the colon cancer.In addition,the Comparative Toxicogenomics Database was searched for known and possible antitumor drugs that may be associated with TNFAIP6.Results:We found that,in most of the cancers included in this analysis,TNFAIP6 was highly expressed,and there is a distinct relationship between TNFAIP6 expression and cancer prognosis.TNFAIP6 expression is associated with cancer-associated fibroblasts,neutrophils,and endothelial cells.TNFAIP6 and similar genes may also be involved in the PID_VEGF_VEGFR_pathway.Immunohistochemistry revealed an increasing trend of TNFAIP6 protein expression in normal,adenoma,and colon cancer tissues.Several known and possible antitumor drugs that may be associated with TNFAIP6 were identified in the Comparative Toxicogenomics Database.These results suggest that a number of drugsmay target TNFAIP6 during cancer treatment,including cisplatin,irinotecan,resveratrol,U 0126,NSC689534,genistein,NSC668394,oxaliplatin,plerixafor,topotecan,vincristine,flutamide,doxorubicin,MRK 003,folic acid,demecolcine,tunicamycin,zoledronic acid,and schizandrin B.Conclusions:TNFAIP6 may function as an oncogene in certain cancers.Furthermore,this study provides evidence that TNFAIP6 is an important factor in colon cancer progression. 展开更多
关键词 CANCER IHC MUTATION SURVIVAL tnfaip6
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牦牛TNFAIP6基因克隆及其在卵巢活动中的时序表达 被引量:1
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作者 马鸿程 熊显荣 +3 位作者 穆松银 海卓 秦文昌 李键 《生物技术通报》 CAS CSCD 北大核心 2019年第11期46-54,共9页
旨在探讨牦牛TNFAIP6基因的序列特征,比较分析其在牦牛不同组织以及发情周期卵巢中的时序表达差异性。采集健康雌性牦牛的心脏、肺脏、脾脏、肾脏、肝脏、子宫、小肠、胃、肌肉和不同发情期的卵巢组织,提取各组织总RNA和总蛋白,通过RT-... 旨在探讨牦牛TNFAIP6基因的序列特征,比较分析其在牦牛不同组织以及发情周期卵巢中的时序表达差异性。采集健康雌性牦牛的心脏、肺脏、脾脏、肾脏、肝脏、子宫、小肠、胃、肌肉和不同发情期的卵巢组织,提取各组织总RNA和总蛋白,通过RT-PCR技术克隆获得牦牛TNFAIP6基因序列并对其进行生物信息学分析,用半定量PCR检测其在牦牛不同组织中的表达水平,Western blot和qRT-PCR法分别检测其在不同发情期牦牛卵巢中的蛋白和mRNA表达水平,并进行统计学分析。克隆获得牦牛TNFAIP6基因CDS区全长830 bp,共编码279个氨基酸。蛋白质分析显示,TNFAIP6蛋白为亲水酸性稳定蛋白,无跨膜结构但有信号肽,其中包含Link和CUB两个结构域,其二级结构和三级结构主要由无规卷曲和α-螺旋组成。通过同源性比对分析,发现牦牛TNFAIP6基因与野牦牛和黄牛的同源性较高。半定量PCR结果显示,TNFAIP6基因在牦牛各组织中均有表达,其中在卵巢、子宫、脾脏和肌肉组织中表达显著高于其他组织。qRT-PCR结果显示,TNFAIP6基因在卵泡期卵巢中的表达水平极显著高于其他两个时期(P<0.01),而红体期与黄体期的表达水平差异不显著(P>0.05)。Western blot结果与qRT-PCR结果基本一致。提示TNFAIP6基因可能参与牦牛卵巢活动调控,为进一步探讨TNFAIP6基因在牦牛卵巢活动中的作用机制提供基础资料。 展开更多
关键词 牦牛 卵巢 tnfaip6 时序表达
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儿童系统性红斑狼疮关键生物标志物的鉴定
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作者 王晓楠 杜玮 +1 位作者 郁春艳 邓为民 《天津医科大学学报》 2025年第1期10-18,共9页
目的:基于生物信息数据库进行数据挖掘,探究儿童系统性红斑狼疮(cSLE)发生的关键基因并构建风险评分模型。方法:从基因数据库中提取cSLE数据,通过多种机器学习识别与cSLE发病相关的基因并构建风险评分模型。通过ELISA验证基因表达,并利... 目的:基于生物信息数据库进行数据挖掘,探究儿童系统性红斑狼疮(cSLE)发生的关键基因并构建风险评分模型。方法:从基因数据库中提取cSLE数据,通过多种机器学习识别与cSLE发病相关的基因并构建风险评分模型。通过ELISA验证基因表达,并利用流式细胞术分析TNFAIP6对细胞凋亡和周期的影响。结果:TNFAIP6、B4GALT5、HLX、ANXA3和DYSF与cSLE发病相关,且对cSLE具有较强的诊断价值,其曲线下面积分别为:TNFAIP6:0.866、B4GALT5:0.891、HLX:0.914、ANXA3:0.878、DYSF:0.929。利用TNFAIP6和DYSF构建的风险评分模型能够有效诊断cSLE(曲线下面积:0.969)。与低风险组相比,中性粒细胞在高风险组中显著增加(t=268.5,P=0.009)。实验结果表明TNFAIP6在cSLE患者血清中高表达,且沉默其表达能够促进THP-1细胞凋亡和阻滞细胞周期。结论:利用TNFAIP6和DYSF构建的cSLE风险评分模型可有效识别cSLE;TNFAIP6可能是cSLE潜在的生物标志物。 展开更多
关键词 儿童系统性红斑狼疮 风险评分模型 tnfaip6 细胞凋亡 细胞周期
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补肾法对控制性超促排小鼠卵丘扩展分级及相关因子HAS2、TNFAIP6的影响 被引量:4
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作者 梁潇 佟雪 +1 位作者 杜惠兰 段彦苍 《北京中医药大学学报》 CAS CSCD 北大核心 2020年第1期35-42,共8页
目的研究补肾调经Ⅱ号方、Ⅲ号方序贯给药对小鼠卵丘卵母细胞复合物(COCs)卵丘扩展分级情况及卵丘扩展相关因子透明质酸合成酶2(HAS2)、肿瘤坏死因子α刺激因子-6(TNFAIP6)表达的影响。方法将120小鼠随机分为正常组、模型组、补肾组。... 目的研究补肾调经Ⅱ号方、Ⅲ号方序贯给药对小鼠卵丘卵母细胞复合物(COCs)卵丘扩展分级情况及卵丘扩展相关因子透明质酸合成酶2(HAS2)、肿瘤坏死因子α刺激因子-6(TNFAIP6)表达的影响。方法将120小鼠随机分为正常组、模型组、补肾组。模型组、补肾组第1~9天腹腔注射醋酸丙氨瑞林(GnRHa),第9天同时注射血清促性腺激素(PMSG),48 h后注射绒毛膜促性腺激素(hCG),正常组注射等体积生理盐水;补肾组第1~9天灌胃补肾调经Ⅱ号方,第10~11天灌胃补肾调经Ⅲ号方,正常组与模型组灌胃等体积蒸馏水。注射生理盐水或hCG 6、9、12 h后在体式显微镜下取出卵丘卵母细胞复合物(COCs),观察卵丘扩展分级并计数,收集COCs,免疫荧光染色、实时荧光定量PCR检测卵丘扩展相关因子蛋白及mRNA的表达。结果与正常组相比,模型组的卵丘扩展分级情况及卵丘扩展相关因子的mRNA表达水平差异无统计学意义(P>0.05);与正常组和模型组相比,补肾组的卵丘扩展分级呈现低级别扩展率降低、高级别扩展率升高的特点(P<0.05);注射生理盐水或hCG 6 h,正常组、模型组和补肾组3组间HAS2 mRNA的表达水平差异无统计学意义(P>0.05);注射生理盐水或hCG 9、12 h,与正常组和模型组相比,补肾组HAS2 mRNA的表达水平升高(P<0.05);注射生理盐水或hCG6、9、12 h,补肾组TNFAIP6 mRNA的表达水平升高(P<0.05)。结论补肾调经Ⅱ号方、Ⅲ号方序贯给药可促进小鼠COCs的卵丘扩展,推测其可能的机制与上调卵丘扩展相关因子HAS2、TNFAIP6 mRNA的表达有关。 展开更多
关键词 补肾调经方Ⅱ号方 补肾调经Ⅲ号方 卵丘卵母细胞复合物 卵丘扩展 透明质酸合成酶2 肿瘤坏死因子α刺激因子-6 小鼠
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