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在早期化学性肝癌发生过程中,与IkappaB降解模式相关的NF-κB持续激活。

Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis.

作者信息

García-Román Rebeca, Pérez-Carreón Julio Isael, Márquez-Quiñones Adriana, Salcido-Neyoy Martha Estela, Villa-Treviño Saúl

机构信息

Departamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN, México DF, México.

出版信息

J Carcinog. 2007 Apr 19;6:5. doi: 10.1186/1477-3163-6-5.

Abstract

BACKGROUND

To define the NF-kappaB activation in early stages of hepatocarcinogenesis and its IkappaB's degradation profiles in comparison to sole liver regeneration.

METHODS

Western-blot and EMSA analyses were performed for the NF-kappaB activation. The transcriptional activity of NF-kappaB was determined by RT-PCR of the IkappaB-alpha mRNA. The IkappaB's degradation proteins were determined by Western-blot assay.

RESULTS

We demonstrated the persistent activation of NF-kappaB during early stages of hepatocarcinogenesis, which reached maximal level 30 min after partial hepatectomy. The DNA binding and transcriptional activity of NF-kappaB, were sustained during early steps of hepatocarcinogenesis in comparison to only partial hepatectomy, which displayed a transitory NF-kappaB activation. In early stages of hepatocarcinogenesis, the IkappaB-alpha degradation turned out to be acute and transitory, but the low levels of IkappaB-beta persisted even 15 days after partial hepatectomy. Interestingly, IkappaB-beta degradation is not induced after sole partial hepatectomy.

CONCLUSION

We propose that during liver regeneration, the transitory stimulation of the transcription factor response, assures blockade of NF-kappaB until recovery of the total mass of the liver and the persistent NF-kappaB activation in early hepatocarcinogenesis may be due to IkappaB-beta and IkappaB-alpha degradation, mainly IkappaB-beta degradation, which contributes to gene transcription related to proliferation required for neoplastic progression.

摘要

背景

为了明确肝癌发生早期阶段核因子κB(NF-κB)的激活情况及其抑制蛋白κB(IkappaB)的降解情况,并与单纯肝脏再生进行比较。

方法

采用蛋白质免疫印迹法(Western-blot)和电泳迁移率变动分析(EMSA)检测NF-κB的激活情况。通过逆转录聚合酶链反应(RT-PCR)检测IkappaB-α信使核糖核酸(mRNA)来确定NF-κB的转录活性。采用Western-blot检测IkappaB的降解蛋白。

结果

我们证实在肝癌发生早期阶段NF-κB持续激活,在部分肝切除术后30分钟达到最高水平。与仅进行部分肝切除(显示短暂的NF-κB激活)相比,NF-κB的DNA结合及转录活性在肝癌发生早期阶段持续存在。在肝癌发生早期阶段,IkappaB-α降解是急性且短暂的,但即使在部分肝切除术后15天,IkappaB-β仍维持低水平。有趣的是,单纯部分肝切除术后不会诱导IkappaB-β降解。

结论

我们提出,在肝脏再生过程中,转录因子反应的短暂刺激确保了NF-κB的阻断,直至肝脏总质量恢复;而在肝癌发生早期阶段NF-κB的持续激活可能是由于IkappaB-β和IkappaB-α的降解,主要是IkappaB-β的降解,这有助于肿瘤进展所需的与增殖相关的基因转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ce/1865534/443d2debbb07/1477-3163-6-5-1.jpg

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