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Heme oxygenase‐1 attenuates the inhibitory effect of bortezomib against the APRIL‐NF‐κB‐CCL3 signaling pathways in multiple myeloma cells: Corelated with bortezomib tolerance in multiple myeloma
Author(s) -
He Zheng C.,
Li Xin Y.,
Guo Yong L.,
Ma Dan,
Fang Qin,
Ren Ling L.,
Zhang Zhao Y.,
Wang Weili,
Yu Zheng Y.,
Zhao Peng,
Wang Ji S.
Publication year - 2019
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.27879
Subject(s) - bortezomib , ccl3 , heme oxygenase , chemistry , cancer research , multiple myeloma , hemin , cytokine , nfkb1 , chemokine , heme , microbiology and biotechnology , immunology , biology , receptor , transcription factor , ccl2 , biochemistry , enzyme , gene
Osteoclasts (OCs) play an essential role in bone destruction in patients with multiple myeloma (MM). Bortezomib can ameliorate bone destruction in patients with MM, but advanced MM often resists bortezomib. We studied the molecular mechanisms of bortezomib tolerance in MM. The expression of the MM‐related genes in newly diagnosed patients with MM and normal donors were studied. C‐C motif chemokine ligand 3 (CCL3) is a cytokine involved in the differentiation of OCs, and its expression is closely related to APRIL (a proliferation‐inducing ligand). We found that bortezomib treatment inhibited APRIL and CCL3. But the heme oxygenase‐1 (HO‐1) activator hemin attenuated the inhibitory effects of bortezomib on APRIL and CCL3. We induced mononuclear cells to differentiate into OCs, and the enzyme‐linked immunosorbent assay showed that the more OCs differentiated, the higher the levels CCL3 secretions detected. Animal experiments showed that hemin promoted MM cell infiltration in mice. The weight and survival rate of tumor mice were associated with HO‐1 expression. Immunohistochemical staining showed that HO‐1, APRIL, and CCL3 staining were positively stained in the tumor infiltrating sites. Then, MM cells were transfected with L‐HO‐1/si‐HO‐1 expression vectors and cultured with an nuclear factor (NF)‐kappa B (κB) pathway inhibitor, QNZ. The results showed that HO‐1 was the upstream gene of APRIL, NF‐κB, and CCL3. We showed that HO‐1 could attenuate the inhibitory effect of bortezomib against the APRIL‐NF‐κB‐CCL3 signaling pathways in MM cells, and the tolerance of MM cells to bortezomib and the promotion of bone destruction are related to HO‐1.