TY - JOUR
T1 - NK cells control tumor-promoting function of neutrophils in mice
AU - Ogura, Keisuke
AU - Sato-Matsushita, Marimo
AU - Yamamoto, Seiji
AU - Hori, Takashi
AU - Sasahara, Masakiyo
AU - Iwakura, Yoichiro
AU - Saiki, Ikuo
AU - Tahara, Hideaki
AU - Hayakawa, Yoshihiro
N1 - Publisher Copyright:
© 2018 American Association for Cancer Research.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Although natural killer (NK) cells are recognized as direct antitumor effectors, the ability of NK cells to control cancer-associated inflammation, which facilitates tumor progression, remains unknown. In this study, we demonstrate that NK cells control tumor-promoting inflammation through functional modificationofneutrophils.NKcellscontrolthetumor-promoting function of neutrophils through an IFNg-dependent mechanism. TumorprogressioninanNKcell–depletedhostisdiminishedwhen the IL17A–neutrophil axis is absent. In NK cell–depleted mice, neutrophils acquire a tumor-promoting phenotype, characterized by upregulation of VEGF-A expression, which promotes tumor growth and angiogenesis. A VEGFR inhibitor which preferentially suppressed tumor growth in NK cell–depleted mice was dependent on neutrophils. Furthermore, the systemic neutropenia caused by an antimetabolite treatment showed an anticancer effect only in mice lacking NK cells. Thus, NK cells likely control the tumor-promoting and angiogenic function of neutrophils.
AB - Although natural killer (NK) cells are recognized as direct antitumor effectors, the ability of NK cells to control cancer-associated inflammation, which facilitates tumor progression, remains unknown. In this study, we demonstrate that NK cells control tumor-promoting inflammation through functional modificationofneutrophils.NKcellscontrolthetumor-promoting function of neutrophils through an IFNg-dependent mechanism. TumorprogressioninanNKcell–depletedhostisdiminishedwhen the IL17A–neutrophil axis is absent. In NK cell–depleted mice, neutrophils acquire a tumor-promoting phenotype, characterized by upregulation of VEGF-A expression, which promotes tumor growth and angiogenesis. A VEGFR inhibitor which preferentially suppressed tumor growth in NK cell–depleted mice was dependent on neutrophils. Furthermore, the systemic neutropenia caused by an antimetabolite treatment showed an anticancer effect only in mice lacking NK cells. Thus, NK cells likely control the tumor-promoting and angiogenic function of neutrophils.
UR - http://www.scopus.com/inward/record.url?scp=85047781262&partnerID=8YFLogxK
U2 - 10.1158/2326-6066.CIR-17-0204
DO - 10.1158/2326-6066.CIR-17-0204
M3 - 学術論文
C2 - 29362222
AN - SCOPUS:85047781262
SN - 2326-6066
VL - 6
SP - 348
EP - 357
JO - Cancer Immunology Research
JF - Cancer Immunology Research
IS - 3
ER -