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BAX/BAK 样蛋白 BOK 是结直肠癌的预后标志物。

The BAX/BAK-like protein BOK is a prognostic marker in colorectal cancer.

机构信息

Department of Physiology and Medical Physics, Centre for Systems Medicine, Royal College of Surgeons in Ireland, Dublin 2, Ireland.

Department of Biomedical Sciences, University of Padova, Padova, Italy.

出版信息

Cell Death Dis. 2018 Jan 26;9(2):125. doi: 10.1038/s41419-017-0140-2.

Abstract

The intrinsic or mitochondrial apoptosis pathway is controlled by the interaction of antiapoptotic and pro-apoptotic members of the BCL-2 protein family. Activation of this death pathway plays a crucial role in cancer progression and chemotherapy responses. The BCL-2-related ovarian killer (BOK) possesses three BCL-2 homology domains and has been proposed to act in a similar pro-apoptotic pathway as the pro-apoptotic proteins BAX and BAK. In this study, we showed that stage II and III colorectal cancer patients possessed decreased levels of BOK protein in their tumours compared to matched normal tissue. BOK protein levels in tumours were also prognostic of clinical outcome but increased BOK protein levels surprisingly associated with earlier disease recurrence and reduced overall survival. We found no significant association of BOK protein tumour levels with ER stress markers GRP78 or GRP94 or with cleaved caspase-3. In contrast, BOK protein levels correlated with Calreticulin. These data indicate BOK as a prognostic marker in colorectal cancer and suggest that different activities of BOK may contribute to cancer progression and prognosis.

摘要

内在的或线粒体凋亡途径受 BCL-2 蛋白家族的抗凋亡和促凋亡成员的相互作用控制。这种死亡途径的激活在癌症进展和化疗反应中起着至关重要的作用。BCL-2 相关卵巢杀手 (BOK) 具有三个 BCL-2 同源结构域,被提议在与促凋亡蛋白 BAX 和 BAK 相似的促凋亡途径中发挥作用。在这项研究中,我们表明,与匹配的正常组织相比,II 期和 III 期结直肠癌患者的肿瘤中 BOK 蛋白水平降低。肿瘤中 BOK 蛋白水平也与临床结局相关,但令人惊讶的是,增加的 BOK 蛋白水平与疾病早期复发和总生存期降低相关。我们没有发现 BOK 蛋白肿瘤水平与 ER 应激标志物 GRP78 或 GRP94 或 cleaved caspase-3 之间有显著关联。相比之下,BOK 蛋白水平与钙网蛋白相关。这些数据表明 BOK 是结直肠癌的预后标志物,并表明 BOK 的不同活性可能有助于癌症的进展和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62c8/5833733/ed61b825cad3/41419_2017_140_Fig1_HTML.jpg

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