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组胺释放因子/翻译调控肿瘤蛋白在非霍奇金淋巴瘤的诱导细胞黏附、抗凋亡和化疗耐药中发挥作用。

Histamine-releasing factor/translationally controlled tumor protein plays a role in induced cell adhesion, apoptosis resistance and chemoresistance in non-Hodgkin lymphomas.

作者信息

He Song, Huang Yuejiao, Wang Yuchan, Tang Jie, Song Yan, Yu Xiafei, Ma Jing, Wang Shitao, Yin Haibing, Li Qiuyue, Ji Lili, Xu Xiaohong

机构信息

Department of Oncology, Affiliated Cancer Hospital of Nantong University, Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target , Nantong, Jiangsu , China.

出版信息

Leuk Lymphoma. 2015 Jul;56(7):2153-61. doi: 10.3109/10428194.2014.981173. Epub 2015 Jan 27.

Abstract

Mounting evidence has proved that cellular adhesion confers resistance to chemotherapy in multiple lymphomas. The molecular mechanism underlying cell adhesion-mediated drug resistance (CAM-DR) is, however, poorly understood. In this study, we investigated the expression and biologic function of histamine-releasing factor (HRF) in non-Hodgkin lymphomas (NHLs). Clinically, by immunohistochemistry analysis we observed obvious up-regulation of HRF in NHLs including diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL) and natural killer (NK)/T-cell lymphoma. Functionally, overexpression and knockdown of HRF demonstrated the antiapoptotic effect of HRF in NHL cells, which may be associated with activation of the p-CREB/BCL-2 signaling pathway. Moreover, cell adhesion assay demonstrated that adhesion to fibronectin (FN) or HS-5 up-regulated HRF expression, while knockdown of HRF resulted in decreased cell adhesion, which led to reversed CAM-DR. Our finding supports the role of HRF in NHL cell apoptosis, adhesion and drug resistance, and may provide a clinical therapeutic target for CAM-DR in NHL.

摘要

越来越多的证据表明,细胞黏附赋予多种淋巴瘤对化疗的抗性。然而,细胞黏附介导的耐药性(CAM-DR)背后的分子机制仍知之甚少。在本研究中,我们调查了组胺释放因子(HRF)在非霍奇金淋巴瘤(NHL)中的表达及生物学功能。临床上,通过免疫组织化学分析,我们观察到HRF在NHL中明显上调,包括弥漫性大B细胞淋巴瘤(DLBCL)、滤泡性淋巴瘤(FL)和自然杀伤(NK)/T细胞淋巴瘤。在功能上,HRF的过表达和敲低证明了HRF在NHL细胞中的抗凋亡作用,这可能与p-CREB/BCL-2信号通路的激活有关。此外,细胞黏附试验表明,与纤连蛋白(FN)或HS-5黏附会上调HRF表达,而敲低HRF会导致细胞黏附减少,从而逆转CAM-DR。我们的发现支持了HRF在NHL细胞凋亡、黏附和耐药中的作用,并可能为NHL中CAM-DR提供临床治疗靶点。

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