TY - JOUR
T1 - A major component of vitamin E, α-tocopherol inhibits the anti-tumor activity of crizotinib against cells transformed by EML4-ALK
AU - Uchihara, Yuki
AU - Kidokoro, Takayuki
AU - Tago, Kenji
AU - Mashino, Tadahiko
AU - Tamura, Hiroomi
AU - Funakoshi-Tago, Megumi
N1 - Funding Information:
We thank Pfizer for the gifted crizotinib (PF-02341066; Xalkori). We thank Dr. H Mano (Graduate School of Medicine, The University of Tokyo) for the gifted pMX-ires-CD8-EML4-ALK. This work was supported in part by grants from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan ( 17K08286 ) and the NOVARTIS Foundation (Japan) for the promotion of Science.
Funding Information:
We thank Pfizer for the gifted crizotinib (PF-02341066; Xalkori). We thank Dr. H Mano (Graduate School of Medicine, The University of Tokyo) for the gifted pMX-ires-CD8-EML4-ALK. This work was supported in part by grants from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan (17K08286) and the NOVARTIS Foundation (Japan) for the promotion of Science.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/4/15
Y1 - 2018/4/15
N2 - Crizotinib is an inhibitor of anaplastic lymphoma kinase (ALK) and is of significant therapeutic benefit to patients with non-small cell lung cancer (NSCLC) harboring the EML4-ALK fusion gene. In the present study, we demonstrated that α-tocopherol, a major component of vitamin E, attenuated the effects of crizotinib independently of its anti-oxidant properties. α-Tocopherol significantly inhibited crizotinib-induced apoptosis in cells transformed by EML4-ALK. It also effectively attenuated the crizotinib-induced inhibition of EML4-ALK and its downstream molecules, STAT3 and ERK, and suppressed the inhibitory effects of crizotinib on EML4-ALK-mediated transformation in the focus formation assay. On the other hand, other members of the vitamin E family, namely, β-tocopherol, γ-tocopherol, δ-tocopherol, and α-tocotrienol, and a water-soluble analog of vitamin E, Trolox had no effects on the anti-tumor activity of crizotinib in cells transformed by EML4-ALK. Collectively, these results revealed the risk of the anti-tumor activity of crizotinib being attenuated when it is administrated in combination with vitamin E supplements containing α-tocopherol as a major component.
AB - Crizotinib is an inhibitor of anaplastic lymphoma kinase (ALK) and is of significant therapeutic benefit to patients with non-small cell lung cancer (NSCLC) harboring the EML4-ALK fusion gene. In the present study, we demonstrated that α-tocopherol, a major component of vitamin E, attenuated the effects of crizotinib independently of its anti-oxidant properties. α-Tocopherol significantly inhibited crizotinib-induced apoptosis in cells transformed by EML4-ALK. It also effectively attenuated the crizotinib-induced inhibition of EML4-ALK and its downstream molecules, STAT3 and ERK, and suppressed the inhibitory effects of crizotinib on EML4-ALK-mediated transformation in the focus formation assay. On the other hand, other members of the vitamin E family, namely, β-tocopherol, γ-tocopherol, δ-tocopherol, and α-tocotrienol, and a water-soluble analog of vitamin E, Trolox had no effects on the anti-tumor activity of crizotinib in cells transformed by EML4-ALK. Collectively, these results revealed the risk of the anti-tumor activity of crizotinib being attenuated when it is administrated in combination with vitamin E supplements containing α-tocopherol as a major component.
KW - Crizotinib
KW - EML4-ALK
KW - NSCLC
KW - Vitamin E
KW - α-tocopherol
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U2 - 10.1016/j.ejphar.2018.02.012
DO - 10.1016/j.ejphar.2018.02.012
M3 - Article
C2 - 29444468
AN - SCOPUS:85042113499
SN - 0014-2999
VL - 825
SP - 1
EP - 9
JO - European journal of pharmacology
JF - European journal of pharmacology
ER -