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自闭症与癌症共享风险基因、信号通路和药物靶点。

Autism and Cancer Share Risk Genes, Pathways, and Drug Targets.

作者信息

Crawley Jacqueline N, Heyer Wolf-Dietrich, LaSalle Janine M

机构信息

MIND Institute, School of Medicine, University of California Davis, Sacramento, CA 95817, USA; Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California Davis, Sacramento, CA 95817, USA.

Department of Microbiology and Molecular Genetics, University of California Davis, Davis, CA 95616, USA; Comprehensive Cancer Center, University of California Davis, Sacramento, CA, 95817, USA.

出版信息

Trends Genet. 2016 Mar;32(3):139-146. doi: 10.1016/j.tig.2016.01.001. Epub 2016 Jan 29.

DOI:10.1016/j.tig.2016.01.001
PMID:26830258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4769654/
Abstract

Autism is a neurodevelopmental disorder, diagnosed behaviorally by social and communication deficits, repetitive behaviors, and restricted interests. Recent genome-wide exome sequencing has revealed extensive overlap in risk genes for autism and for cancer. Understanding the genetic commonalities of autism(s) and cancer(s), with a focus on mechanistic pathways, could lead to repurposed therapeutics.

摘要

自闭症是一种神经发育障碍,通过社交和沟通缺陷、重复行为以及受限兴趣进行行为学诊断。最近的全基因组外显子测序揭示了自闭症和癌症的风险基因存在广泛重叠。了解自闭症和癌症的遗传共性,重点关注机制途径,可能会带来重新利用的疗法。

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本文引用的文献

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Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.泛素蛋白连接酶E3A的表观遗传调控及其在人类神经发育障碍中的作用。
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Risk of cancer in children, adolescents, and young adults with autistic disorder.患有自闭症谱系障碍的儿童、青少年和青年患癌症的风险。
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The contribution of de novo coding mutations to autism spectrum disorder.新生编码突变对自闭症谱系障碍的影响。
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Synaptic, transcriptional and chromatin genes disrupted in autism.在自闭症中受到破坏的突触、转录和染色质基因。
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