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Wilms' tumor 1-associating protein plays an aggressive role in diffuse large B-cell lymphoma and forms a complex with BCL6 via Hsp90.

Authors :
Kuai Y
Gong X
Ding L
Li F
Lei L
Gong Y
Liu Q
Tan H
Zhang X
Liu D
Ren G
Pan H
Shi Y
Berberich-Siebelt F
Mao Z
Zhou R
Source :
Cell communication and signaling : CCS [Cell Commun Signal] 2018 Aug 24; Vol. 16 (1), pp. 50. Date of Electronic Publication: 2018 Aug 24.
Publication Year :
2018

Abstract

Background: Wilms' tumor 1-associating protein (WTAP) is a nuclear protein, which is ubiquitously expressed in many tissues. Furthermore, in various types of malignancies WTAP is overexpressed and plays a role as an oncogene. The function of WTAP in diffuse large B-cell lymphoma (DLBCL), however, remains unclear.<br />Methods: Immunohistochemistry was applied to evaluate the levels of WTAP expression in DLBCL tissues and normal lymphoid tissues. Overexpression and knock-down of WTAP in DLBCL cell lines, verified on mRNA and protein level served to analyze cell proliferation and apoptosis in DLBCL cell lines by flow cytometry. Finally, co-immunoprecipitation (Co-IP), IP, and GST-pull down assessed the interaction of WTAP with Heat shock protein 90 (Hsp90) and B-cell lymphoma 6 (BCL6) as well as determined the extend of its ubiquitinylation.<br />Results: WTAP protein levels were consistently upregulated in DLBCL tissues. WTAP promoted DLBCL cell proliferation and improved the ability to confront apoptosis, while knockdown of WTAP in DLBCL cell lines allowed a significant higher apoptosis rate after treatment with Etoposide, an anti-tumor drug. The stable expression of WTAP was depended on Hsp90. In line, we demonstrated that WTAP could form a complex with BCL6 via Hsp90 in vivo and in vitro.<br />Conclusion: WTAP is highly expressed in DLBCL, promoting growth and anti-apoptosis in DLBCL cell lines. WTAP is a client protein of Hsp90 and can appear in a complex with BCL6 and Hsp90 in DLBCL. Down-regulation of WTAP could improve the chemotherapeutic treatments in DLBCL.

Details

Language :
English
ISSN :
1478-811X
Volume :
16
Issue :
1
Database :
MEDLINE
Journal :
Cell communication and signaling : CCS
Publication Type :
Academic Journal
Accession number :
30143009
Full Text :
https://doi.org/10.1186/s12964-018-0258-6