Targeting nucleotide metabolism as the nexus of viral infections, cancer, and the immune response

被引:52
|
作者
Ariav, Yarden [1 ]
Ch'ng, James H. [2 ]
Christofk, Heather R. [3 ]
Ron-Harel, Noga [4 ]
Erez, Ayelet [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Regulat, Rehovot, Israel
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Hematol Oncol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
[4] Technion Israel Inst Technol, Dept Biol, Haifa, Israel
关键词
ANTIVIRAL ACTIVITY; DNA-SYNTHESIS; HUMAN-CELLS; CAD GENE; VIRUS; MECHANISM; MYC; MODE; ACTIVATION; RIBAVIRIN;
D O I
10.1126/sciadv.abg6165
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Virus-infected cells and cancers share metabolic commonalities that stem from their insatiable need to replicate while evading the host immune system. These similarities include hijacking signaling mechanisms that induce metabolic rewiring in the host to up-regulate nucleotide metabolism and, in parallel, suppress the immune response. In both cancer and viral infections, the host immune cells and, specifically, lymphocytes augment nucleotide synthesis to support their own proliferation and effector functions. Consequently, established treatment modalities targeting nucleotide metabolism against cancers and virally infected cells may result in restricted immune response. Encouragingly, following the introduction of immunotherapy against cancers, multiple studies improved our understanding for improving antigen presentation to the immune system. We propose here that understanding the immune consequences of targeting nucleotide metabolism against cancers may be harnessed to optimize therapy against viral infections.
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页数:8
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