| Literature DB >> 27101149 |
Haibing Yin1, Xiaobing Miao1, Yaxun Wu1, Yingze Wei1, Guijuan Zong1, Shuyun Yang1, Xudong Chen1, Guihua Zheng1, Xinghua Zhu1, Yan Guo1, Chunsun Li1, Yali Chen1, Yuchan Wang2, Song He3.
Abstract
The chaperonin containing t-complex polypeptide 1 (CCT) is known to mediate folding of proteins. CCT, subunit 8 (CCT8), is the θ subunit of CCT complex chaperonin. CCT8 has been reported to be dysregulated in several tumor tissues. In this study, we investigated the role of CCT8 in B-cell non-Hodgkin's lymphoma (NHL). Clinically, the expression levels of CCT8 in reactive lymphoid hyperplasia (RLH) and B-cell NHL specimens were investigated using immunohistochemical analysis. We found that CCT8 was highly expressed in proliferating germinal center cells compared with the quiescent cells of the follicular mantle zone. Furthermore, CCT8 was highly expressed in progressive lymphomas than in indolent lymphomas. Kaplan-Meier curve showed that high expression of CCT8 was significantly associated with shorter overall survival in patients with diffuse large B-cell lymphoma. Moreover, we demonstrated that CCT8 could promote the proliferation of B-cell NHL cells. In addition, we found that CCT8 could accelerate the G1/S transition in B-cell NHL. Finally, we demonstrated that overexpression of CCT8 could reverse cell adhesion-mediated drug resistance (CAM-DR) phenotype. Our study may shed new insights into the important role of CCT8 in cancer development.Entities:
Keywords: B-cell non-Hodgkin's lymphoma; CCT8; Cell adhesion-mediated drug resistance (CAM-DR); Cell cycle; Proliferation
Mesh:
Substances:
Year: 2016 PMID: 27101149 DOI: 10.1016/j.leukres.2016.04.010
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156