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

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.
AuthorsSong He, Yuejiao Huang, Yuchan Wang, Jie Tang, Yan Song, Xiafei Yu, Jing Ma, Shitao Wang, Haibing Yin, Qiuyue Li, Lili Ji, Xiaohong Xu
JournalLeukemia & lymphoma (Leuk Lymphoma) Vol. 56 Issue 7 Pg. 2153-61 (Jul 2015) ISSN: 1029-2403 [Electronic] United States
PMID25363345 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers, Tumor
  • RNA, Small Interfering
  • Tumor Protein, Translationally-Controlled 1
Topics
  • Apoptosis
  • Biomarkers, Tumor (antagonists & inhibitors, genetics, metabolism)
  • Blotting, Western
  • Cell Adhesion
  • Cell Proliferation
  • Drug Resistance, Neoplasm
  • Flow Cytometry
  • Humans
  • Immunoenzyme Techniques
  • Lymphoma, Non-Hodgkin (drug therapy, metabolism, pathology)
  • RNA, Small Interfering (genetics)
  • Signal Transduction
  • Tumor Cells, Cultured
  • Tumor Protein, Translationally-Controlled 1

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