Down-regulated miR-148b increases resistance to CHOP in diffuse large B-cell lymphoma cells by rescuing Ezrin

Biomed Pharmacother. 2018 Oct:106:267-274. doi: 10.1016/j.biopha.2018.06.093. Epub 2018 Jun 28.

Abstract

Background: Aberrant microRNA (miRNAs) have recently been proposed as important regulators in acquiring resistance to cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) in diffuse large B-cell lymphoma (DLBCL). The purpose of this study was to establish the role of miR-148b in the development of CHOP resistance in DLBCL.

Methods: The expression patterns of miR-148b, HDAC6, and Ezrin were detected in CHOP-resistant clinical specimens and a DLBCL cell line. miR-148b, HDAC6, and Ezrin in DLBCL cells were manipulated by cell transfection to explore the functional correlation between them. Cell viability was determined using a CCK-8 assay.

Results: We found that miR-148b levels were markedly reduced and that the protein expressions of HDAC6 and Ezrin were increased in DLBCL CHOP-resistant clinical specimens and the cell line CRL2631/CHOP. Indeed, HDAC6 decreased the acetylation of histones H3 and H4 in the miR-148b promoter to inhibit miR-148b expression in DLBCL. Moreover, down-regulated miR-148b encouraged CHOP resistance in CRL2631 cells and miR-148b sensitized CRL2631 cells. We further revealed that Ezrin was negatively regulated by miR-148b and that the knockdown of Ezrin significantly attenuated CHOP resistance in CRL2631 cells induced by miR-148b silencing. MiR-148b also sensitized CRL2631/CHOP cell xenografts to CHOP in mice.

Conclusion: Our data indicated that the high level of HDAC6 inhibited miR-148b via maintaining the low acetylation of histones H3 and H4 in the miR-148b promoter, thus rescuing Ezrin expression and promoting CHOP resistance in DLBCL.

Keywords: CHOP resistance; DLBCL; Ezrin; HDAC6; MiR-148b.

MeSH terms

  • Acetylation
  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cyclophosphamide / adverse effects
  • Cyclophosphamide / therapeutic use
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Down-Regulation
  • Doxorubicin / adverse effects
  • Doxorubicin / therapeutic use
  • Drug Resistance, Neoplasm* / genetics
  • Female
  • Gene Expression Regulation, Neoplastic
  • Histone Deacetylase 6 / metabolism
  • Histones / metabolism
  • Humans
  • Lymphoma, Large B-Cell, Diffuse / drug therapy*
  • Lymphoma, Large B-Cell, Diffuse / genetics
  • Lymphoma, Large B-Cell, Diffuse / metabolism
  • Lymphoma, Large B-Cell, Diffuse / pathology
  • Male
  • Mice, Inbred BALB C
  • Mice, Nude
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Middle Aged
  • Prednisone / adverse effects
  • Prednisone / therapeutic use
  • Signal Transduction / drug effects
  • Time Factors
  • Treatment Outcome
  • Tumor Burden / drug effects
  • Vincristine / adverse effects
  • Vincristine / therapeutic use
  • Xenograft Model Antitumor Assays

Substances

  • Cytoskeletal Proteins
  • Histones
  • MIRN148 microRNA, human
  • MicroRNAs
  • ezrin
  • Vincristine
  • Doxorubicin
  • Cyclophosphamide
  • HDAC6 protein, human
  • Histone Deacetylase 6
  • Prednisone

Supplementary concepts

  • CHOP protocol