Cancer cell-autonomous contribution of type I interferon signaling to the efficacy of chemotherapy

被引:910
作者
Sistigu, Antonella [1 ,2 ,3 ,4 ,33 ]
Yamazaki, Takahiro [1 ,2 ,3 ,33 ]
Vacchelli, Erika [1 ,3 ,5 ,33 ]
Chaba, Kariman [5 ,6 ,7 ]
Enot, David P. [5 ,6 ,7 ]
Adam, Julien [1 ,8 ,9 ]
Vitale, Ilio [10 ]
Goubar, Aicha [1 ,11 ]
Baracco, Elisa E. [1 ,3 ,5 ]
Remedios, Catarina [1 ,2 ,3 ]
Fend, Laetitia [1 ,2 ,12 ]
Hannani, Dalil [1 ,2 ,3 ]
Aymeric, Laetitia [1 ,2 ,3 ]
Ma, Yuting [1 ,3 ,5 ]
Niso-Santano, Mireia [1 ,3 ,5 ]
Kepp, Oliver [1 ,3 ,5 ]
Schultze, Joachim L. [13 ]
Tueting, Thomas [14 ]
Belardelli, Filippo [4 ]
Bracci, Laura [4 ]
La Sorsa, Valentina [4 ]
Ziccheddu, Giovanna [4 ]
Sestili, Paola [4 ]
Urbani, Francesca [4 ]
Delorenzi, Mauro [15 ,16 ,17 ]
Lacroix-Triki, Magali [18 ]
Quidville, Virginie [1 ]
Conforti, Rosa [1 ,2 ,19 ,20 ]
Spano, Jean-Philippe [20 ]
Pusztai, Lajos [21 ]
Poirier-Colame, Vichnou [1 ,2 ,19 ]
Delaloge, Suzette [1 ,8 ]
Penault-Llorca, Frederique [22 ]
Ladoire, Sylvain [23 ,24 ,25 ]
Arnould, Laurent [23 ,24 ,25 ]
Cyrta, Joanna [1 ]
Dessoliers, Marie-Charlotte [1 ,11 ]
Eggermont, Alexander [3 ]
Bianchi, Marco E. [26 ]
Pittet, Mikael [27 ,28 ]
Engblom, Camilla [27 ,28 ]
Pfirschke, Christina [27 ,28 ]
Preville, Xavier [12 ]
Uze, Gilles [29 ]
Schreiber, Robert D. [30 ]
Chow, Melvyn T. [31 ]
Smyth, Mark J. [31 ,32 ]
Proietti, Enrico
Andre, Fabrice [1 ,3 ,8 ,9 ,11 ]
Kroemer, Guido [1 ,5 ,6 ,7 ,33 ,34 ]
机构
[1] Gustave Roussy Canc Campus, Villejuif, France
[2] INSERM, U1015, Villejuif, France
[3] Univ Paris Saclay, Fac Med, Le Kremlin Bicetre, France
[4] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[5] INSERM, U848, Villejuif, France
[6] Ctr Rech Cordeliers, Equipe Labellisee Ligue Nationale Canc 11, Paris, France
[7] Univ Paris 05, Sorbonne Paris Cite, Paris, France
[8] Gustave Roussy Canc Campus, Dept Biol & Pathol, Villejuif, France
[9] Gustave Roussy Canc Campus, Dept Med Oncol, Villejuif, France
[10] Regina Elena Inst Canc Res, Rome, Italy
[11] INSERM, U981, Villejuif, France
[12] Transgene SA, Illkirch Graffenstaden, France
[13] Univ Bonn, Lab Genom & Immunoregulat Life & Med Sci LIMES, Bonn, Germany
[14] Univ Hosp Bonn, Dept Dermatol, Lab Expt Dermatol, Bonn, Germany
[15] SIB, Lausanne, Switzerland
[16] Ecole Polytech Fed Lausanne, Sch Life Sci, ISREC, Natl Ctr Competence Res NCCR Mol Oncol, Lausanne, Switzerland
[17] CHU Vaudois, Dept Format & Rech, Lausanne, Switzerland
[18] Ctr Claudius Regaud, Dept Pathol, Toulouse, France
[19] Ctr Clin Invest Biotherapies Canc CICBT 507, Villejuif, France
[20] Hop La Pitie Salpetriere, Dept Med Oncol, Paris, France
[21] Yale Univ, Sch Med, New Haven, CT USA
[22] Univ Auvergne, EA ERTICa 4677, Dept Pathol, Jean Perrin Ctr, Clermont Ferrand, France
[23] Ctr Georges Francois Leclerc, Dept Med Oncol, Dijon, France
[24] INSERM, Fac Med CRI 866, Dijon, France
[25] Univ Burgundy, Dijon, France
[26] San Raffaele Univ & Sci Inst, Milan, Italy
[27] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[28] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
[29] Univ Montpellier 2, CNRS, UMR5235, Montpellier, France
[30] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[31] Queensland Inst Med Res, Herston, Qld 4006, Australia
[32] Univ Queensland, Sch Med, Herston, Qld, Australia
[33] Gustave Roussy Canc Campus, Metabol Platform, Villejuif, France
[34] Hop Europeen Georges, AP HP, Paris, France
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; BREAST-CANCER; IMMUNE-RESPONSES; ANTICANCER CHEMOTHERAPY; DENDRITIC CELLS; RIG-I; INNATE; TUMORS; GENE;
D O I
10.1038/nm.3708
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Some of the anti-neoplastic effects of anthracyclines in mice originate from the induction of innate and T cell-mediated anticancer immune responses. Here we demonstrate that anthracyclines stimulate the rapid production of type I interferons (IFNs) by malignant cells after activation of the endosomal pattern recognition receptor Toll-like receptor 3 (TLR3). By binding to IFN-alpha and IFN-beta receptors (IFNARs) on neoplastic cells, type I IFNs trigger autocrine and paracrine circuitries that result in the release of chemokine (C-X-C motif) ligand 10 (CXCL10). Tumors lacking TIr3 or Ifnar failed to respond to chemotherapy unless type I IFN or Cxcl10, respectively, was artificially supplied. Moreover, a type I IFN-related signature predicted clinical responses to anthracycline-based chemotherapy in several independent cohorts of patients with breast carcinoma characterized by poor prognosis. Our data suggest that anthracycline-mediated immune responses mimic those induced by viral pathogens. We surmise that such 'viral mimicry' constitutes a hallmark of successful chemotherapy.
引用
收藏
页码:1301 / 1309
页数:9
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