Role of myeloma-derived MIF in myeloma cell adhesion to bone marrow and chemotherapy response

Zheng Yuhuan, Wang Qiang, Tianshu Li, Jianfei Qian, Yong Lu, Yi Li, Enguang Bi, Frederic Reu, Yu Qin, Judy Drazba, Eric Hsi, Yang Jing, Zhen Cai, Qing Yi

Research output: Contribution to journalArticle

15 Scopus citations

Abstract

Background: Multiple myeloma (MM) remains an incurable cancer characterized by accumulation of malignant plasma cells in the bone marrow (BM). The mechanism underlying MM homing to BM is poorly elucidated. Methods: The clinical significance of migration inhibitory factor (MIF) expression was examined by analyzing six independent gene expression profile databases of primary MM cells using the Student's t test and Kaplan-Meier test. Enzymelinked immunosorbent assay was used to examine MIF expression. In vivo bioluminescent imaging was used to determine MM cell localization and treatment efficacy in human MM xenograft mouse models, with three to four mice per group. MM cell attachment to BM stromal cells (BMSCs) was monitored by cell adhesion assay. MIF regulation of the expression of adhesion molecules was determined by chromatin immunoprecipitation (ChIP) assay. Statistical tests were two-sided. Results: High levels of MIF were detected inMMBM(MIF level in BM plasma: healthy = 10.72 6 5.788 ng/mL, n=5; MM=1811 6 248.7ng/mL, n=10; P < .001) and associated with poor survival of patients (Kaplan-Meier test for MM OS: 87 MIFhigh patients, 86 MIFlow patients, P = .02). Knocking down MIF impairedMMcell adhesion to BMSCs in vitro and led to formation of extramedullary tumors in SCID mice. MIF acted through surface receptor CXCR4 and adaptor COPS5 to regulate the expression of adhesion molecules ALCAM, ITGAV, and ITGB5 onMMcells.More importantly, MIF-deficient MM cells were sensitive to chemotherapy in vitro when cocultured with BMSCs and in vivo. MIF inhibitor 4-IPP sensitized MMcells to chemotherapy. Conclusions: MIF is an important player and a novel therapeutic target in MM. Inhibiting MIF activity will sensitize MM cells to chemotherapy.

Original languageEnglish (US)
JournalJournal of the National Cancer Institute
Volume108
Issue number11
DOIs
StatePublished - Nov 2016

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint Dive into the research topics of 'Role of myeloma-derived MIF in myeloma cell adhesion to bone marrow and chemotherapy response'. Together they form a unique fingerprint.

Cite this