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细胞内透明质酸结合蛋白4(HABP4):结直肠癌中的一种候选肿瘤抑制因子。

Intracellular hyaluronic acid-binding protein 4 (HABP4): a candidate tumor suppressor in colorectal cancer.

作者信息

Melo-Hanchuk Talita Diniz, Colleti Carolina, Saito Ângela, Mendes Maria Carolina Santos, Carvalheira José Barreto Campello, Vassallo Jose, Kobarg Jörg

机构信息

Department of Biochemistry and Tissue Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, SP, Brazil.

These authors contributed equally to this work.

出版信息

Oncotarget. 2020 Nov 17;11(46):4325-4337. doi: 10.18632/oncotarget.27804.

Abstract

Hyaluronic Acid-binding protein 4 (HABP4) is a regulatory protein of 57 kDa that is functionally involved in transcription regulation and RNA metabolism and shows several characteristics common to oncoproteins or tumor suppressors, including altered expression in cancer tissues, nucleus/cytoplasm shuttling, intrinsic lack of protein structure, complex interactomes and post translational modifications. Its gene has been found in a region on chromosome 9q22.3-31, which contains SNP haplotypes occurring in individuals with a high risk for familial colon cancer. To test a possible role of HABP4 in tumorigenesis we generated knockout mice by the CRISPR/Cas9 method and treated the animals with azoxymethane (AOM)/dextran sodium sulfate (DSS) for induction of colon tumors. -/- , compared to wild type mice, had more and larger tumors, and expressed more of the proliferation marker proteins Cyclin-D1, CDK4 and PCNA. Furthermore, the cells of the bottom of the colon crypts in the -/- divided more rapidly. Next, we generated also HABP4/- HCT 116 cells, in cell culture and found again an increased proliferation in clonogenic assays in comparison to wild-type cells. Our study of the protein expression levels of HABP4 in human colon cancer samples, through immunohistochemistry assays, showed, that 30% of the tumors analyzed had low expression of HABP4. Our data suggest that HABP4 is involved in proliferation regulation of colon cells and and that it is a promising new candidate for a tumor suppressor protein that can be explored both in the diagnosis and possibly therapy of colon cancer.

摘要

透明质酸结合蛋白4(HABP4)是一种57 kDa的调节蛋白,在转录调控和RNA代谢中发挥功能作用,具有一些癌蛋白或肿瘤抑制因子共有的特征,包括在癌组织中的表达改变、细胞核/细胞质穿梭、蛋白质结构内在缺失、复杂的相互作用组和翻译后修饰。其基因位于9号染色体9q22.3 - 31区域,该区域包含在家族性结肠癌高危个体中出现的单核苷酸多态性单倍型。为了测试HABP4在肿瘤发生中的可能作用,我们通过CRISPR/Cas9方法生成了基因敲除小鼠,并用氧化偶氮甲烷(AOM)/葡聚糖硫酸钠(DSS)处理这些动物以诱导结肠肿瘤。与野生型小鼠相比,基因敲除小鼠有更多更大的肿瘤,并且增殖标志物蛋白细胞周期蛋白D1、细胞周期蛋白依赖性激酶4(CDK4)和增殖细胞核抗原(PCNA)的表达更多。此外,基因敲除小鼠结肠隐窝底部的细胞分裂更快。接下来,我们在细胞培养中也生成了HABP4基因敲除的HCT 116细胞,并且再次发现与野生型细胞相比,在克隆形成试验中其增殖增加。我们通过免疫组织化学分析对人类结肠癌样本中HABP4蛋白表达水平的研究表明,所分析的肿瘤中有30%的HABP4表达较低。我们的数据表明,HABP4参与结肠细胞的增殖调控,并且它是一种有前景的肿瘤抑制蛋白新候选物,可用于结肠癌的诊断和可能的治疗探索。

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