Evidence map›Paper›PMID 25625930›Full record

ReviewHuman vaccines & immunotherapeutics2014

Mechanisms and pathways of innate immune activation and regulation in health and cancer.

Jun Cui, Yongjun Chen, Helen Y Wang, Rong-Fu Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 175 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

175 citing papers in PubMed, 1 synthesis or guideline pooled it, 310 citations in OpenAlex.

  1. Pooled it
  2. Article
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  6. Challenges and Perspectives in ncRNA Research.Experientia supplementum (2012) · 2026
    Review
  7. Article
  8. Article
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  16. Tumor microenvironment as a complex milieu driving cancer progression: a mini review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
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  19. Review
  20. Article

115 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 3 countries.

Jun Cuia Key Laboratory of Gene Engineering of the Ministry of Education; State Key Laboratory of Biocontrol; School of Life Sciences ; Sun Yat-sen University ; Guangzhou , P. R. China.
Yongjun Chen
Helen Y Wang
Rong-Fu Wang
Houston Methodist · USMinistry of Education of the People's Republic of China · CNSun Yat-sen University · CN

Funding

Novel Strategies for Intervention of Inflammatory Diseases and Cancer - Research Supplement to R01-CA101795R01CA101795 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WANG, RONGFU · 2004 to 2022
$4.6M
Development of Novel Vaccines for Cocaine AbuseR01DA030338 · NIDA · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ORSON, FRANK M, WANG, RONGFU · 2010 to 2014
$1.6M
NCI NIH HHS R01CA09327NCI NIH HHS R01CA101795NIDA NIH HHS DA030338
6 · The paper itself

Abstract

Research on innate immune signaling and regulation has recently focused on pathogen recognition receptors (PRRs) and their signaling pathways. Members of PRRs sense diverse microbial invasions or danger signals, and initiate innate immune signaling pathways, leading to proinflammatory cytokines production, which, in turn, instructs adaptive immune response development. Despite the diverse functions employed by innate immune signaling to respond to a variety of different pathogens, the innate immune response must be tightly regulated. Otherwise, aberrant, uncontrolled immune responses will lead to harmful, or even fatal, consequences. Therefore, it is essential to better discern innate immune signaling and many regulators, controlling various signaling pathways, have been identified. In this review, we focus on the recent advances in our understanding of the activation and regulation of innate immune signaling in the host response to pathogens and cancer.

Indexed as

DNA VirusesHumansImmunity, InnateInflammasomesInterferon Type INeoplasmsRNA VirusesSignal TransductionToll-Like ReceptorsInflammasomesInterferon Type IToll-Like ReceptorsAIM2, absent in melanoma 2ALRs, AIM2-like receptorsAMPK, AMP activated protein kinaseASC, apoptosis-associated speck-like protein containing a CARDAtg16L, autophagy related 16-likeBMM, bone marrow-derived macrophagecancerCARD, caspase recruitment domaincDC, conventional dendritic cellCDNs, cyclic dinucleotidescGAS, cyclic GMP-AMP synthasecIAP, cellular inhibitor of apoptosis proteinCLRs, C-type lectin receptorsCMV, cytomegalovirusCYLD, the familial cylindromatosis tumor suppressor geneDAMPs, danger-associated molecular patternsDCs, dendritic cellsDDX41, DEAD (Asp-Glu-Ala-Asp) box polypeptide 41ER, endoplasmic reticulumGBP5, guanylate-binding protein 5GSK3β, Glycogen synthase kinase 3βHCC, hepatocellular carcinomaiE-DAP, g-D-glutamyl-meso-diaminopimelic acidIFI16, interferon, gamma-inducible protein 16IFN, interferonIKKi, inducible IkB kinaseIKK, IkB kinaseinflammationinnate immunityIRAK, interleukin-1 receptor-associated kinaseIRF, interferon regulatory factorKSHV, Kaposi's sarcoma-associated herpesvirusLBP, LPS-binding proteinLGP 2, laboratory of genetics and physiology 2LPS, lipopolysaccharideLRR, leucine-rich repeatLT, lethal toxinLUBAC, linear ubiquitin assembly complexMAVS, mitochondrial antiviral signaling proteinMDA5, melanoma differentiation-associated protein 5MDP, muramyl dipeptideMIB, mind bombMyD88, myeloid differentiation factor 88NAIPs, neuronal apoptosis inhibitory proteinsNEMO, NF-kB essential modulatorNLRs, Nod- like receptorsNOD, nucleotide-binding oligomerization domainNrdp1, neuregulin receptor degradation protein 1PAMPs, pathogen-associated molecular patternspDC, plasmacytoid dendritic cellPKC-d, protein kinase C deltaPKR, dsRNA-dependent protein kinasePRRsPRRs, pathogen recognition receptorsRACK1, receptor for activated C kinase 1RAUL, RTA-associated E3 ligaseRIG-I, retinoic acid-inducible gene 1RIP, receptor-interacting proteinRLRs, RIG-I-like receptorsROS, reactive oxygen speciesSARM, sterile a- and armadillo motif-containing proteinSIGIRR, single Ig IL-1-related receptorSOCS, suppressor of cytokine signalingSTING, stimulator of interferon geneTAK1, TGF-b-activating kinase 1TANK, TRAF family-member-associated NF-kB activatorTBK1, TANK binding kinase 1TIRAP, TIR domain-containing adapter proteinTIR, Toll IL-1 receptorTLRs, Toll-like receptorsTRAF, TNFR-associated factorTRAILR, tumor-necrosis factor-related apoptosis-inducing ligand receptorTRAM, TRIF-related adaptor moleculeTRIF, TIR domain-containing adaptor inducing IFN-bTRIMs, tripartite motif containing proteinsTRIP, TRAF-interacting proteintype I interferonULK1, autophagy related serine threonine UNC-51- like kinase

Identifiers

PMID25625930
PMCPMC4514086
OpenAlexW1991982546

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.