MYC and Twist1 cooperate to drive metastasis by eliciting crosstalk between cancer and innate immunity

被引:44
作者
Dhanasekaran, Renumathy [1 ]
Baylot, Virginie [2 ,3 ]
Kim, Minsoon [2 ,3 ]
Kuruvilla, Sibu [2 ,3 ]
Bellovin, David, I [2 ,3 ]
Adeniji, Nia [2 ,3 ]
Rajan, Anand [4 ]
Lai, Ian [2 ,3 ]
Gabay, Meital [2 ,3 ]
Tong, Ling [2 ,3 ]
Krishnan, Maya [2 ,3 ]
Park, Jangho [2 ,3 ]
Hu, Theodore [2 ,3 ]
Barbhuiya, Mustafa A. [5 ,6 ,7 ,8 ]
Gentles, Andrew J. [9 ,10 ]
Kannan, Kasthuri [11 ,12 ]
Tran, Phuoc T. [5 ,6 ,7 ,8 ]
Felsher, Dean W. [2 ,3 ]
机构
[1] Stanford Univ, Div Gastroenterol & Hepatol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Div Oncol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pathol, Div Oncol, Stanford, CA 94305 USA
[4] Univ Iowa Hosp & Clin, Dept Pathol, Iowa City, IA 52242 USA
[5] Johns Hopkins Univ, Radiat Oncol & Mol Radiat Sci, Baltimore, MD USA
[6] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[7] Johns Hopkins Univ, Sch Med, James Buchanan Brady Urol Inst, Baltimore, MD USA
[8] Johns Hopkins Univ, Sch Med, Dept Urol, Baltimore, MD 21205 USA
[9] Stanford Univ, Sch Med, Dept Med Biomed Informat, Stanford, CA USA
[10] Stanford Univ, Sch Med, Dept Biomed Data Sci, Stanford, CA USA
[11] NYU Langone Med Ctr, Dept Pathol, New York, NY USA
[12] NYU Langone Med Ctr, Genome Technol Ctr, New York, NY USA
来源
ELIFE | 2020年 / 9卷
关键词
GENE-EXPRESSION; TRANSCRIPTION FACTOR; MONOCLONAL-ANTIBODY; TUMOR PROGRESSION; MACROPHAGES; CELLS; DIFFERENTIATION; INITIATION; PLASTICITY; REGULATOR;
D O I
10.7554/eLife.50731
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metastasis is a major cause of cancer mortality. We generated an autochthonous transgenic mouse model whereby conditional expression of MYC and Twist1 enables hepatocellular carcinoma (HCC) to metastasize in >90% of mice. MYC and Twist1 cooperate and their sustained expression is required to elicit a transcriptional program associated with the activation of innate immunity, through secretion of a cytokinome that elicits recruitment and polarization of tumor associated macrophages (TAMs). Systemic treatment with Ccl2 and Il13 induced MYC-HCCs to metastasize; whereas, blockade of Ccl2 and Il13 abrogated MYC/Twist1-HCC metastasis. Further, in 33 human cancers (n = 9502) MYC and TWIST1 predict poor survival (p=4.3x10(-10)), CCL2/IL13 expression (p<10(-109)) and TAM infiltration (p<10(-96)). Finally, in the plasma of patients with HCC (n = 25) but not cirrhosis (n = 10), CCL2 and IL13 were increased and IL13 predicted invasive tumors. Therefore, MYC and TWIST1 generally appear to cooperate in human cancer to elicit a cytokinome that enables metastasis through crosstalk between cancer and immune microenvironment.
引用
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页数:28
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