Evidence map›Paper›PMID 31156630›Full record

ReviewFrontiers in immunology2019

Role of C5b-9 and RGC-32 in Cancer.

Sonia I Vlaicu, Alexandru Tatomir, Violeta Rus, Horea Rus

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Inside-Out of Complement in Cancer.Frontiers in immunology · 2022
    Review
  16. Article
  17. Targeting the Complement Pathway in Malignant Glioma Microenvironments.Frontiers in cell and developmental biology · 2021
    Review
  18. Review
  19. Article
  20. Review
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 2 institutions in 2 countries.

Sonia I VlaicuDepartment of Internal Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Alexandru TatomirDepartment of Neurology, School of Medicine, University of Maryland, Baltimore, MD, United States.
Violeta RusDivision of Rheumatology and Immunology, Department of Medicine, School of Medicine, University of Maryland, Baltimore, MD, United States.
Horea RusDepartment of Neurology, School of Medicine, University of Maryland, Baltimore, MD, United States.
University of Maryland, Baltimore · USIuliu Hațieganu University of Medicine and Pharmacy · RO

Funding

Regulation of Oligodendrocyte SurvivalR01NS042011 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI RUS, HOREA · 2002 to 2006
$1.2M
Role of RGC-32 in gliosisI01BX001458 · VA · BALTIMORE VA MEDICAL CENTER · PI RUS, HOREA · 2014 to 2019
–
BLRD VA I01 BX001458NINDS NIH HHS R01 NS042011
6 · The paper itself

Abstract

The complement system represents an effective arsenal of innate immunity as well as an interface between innate and adaptive immunity. Activation of the complement system culminates with the assembly of the C5b-9 terminal complement complex on cell membranes, inducing target cell lysis. Translation of this sequence of events into a malignant setting has traditionally afforded C5b-9 a strict antitumoral role, in synergy with antibody-dependent tumor cytolysis. However, in recent decades, a plethora of evidence has revised this view, highlighting the tumor-promoting properties of C5b-9. Sublytic C5b-9 induces cell cycle progression by activating signal transduction pathways (e.g., Gi protein/ phosphatidylinositol 3-kinase (PI3K)/Akt kinase and Ras/Raf1/ERK1) and modulating the activation of cancer-related transcription factors, while shielding malignant cells from apoptosis. C5b-9 also induces Response Gene to Complement (RGC)-32, a gene that contributes to cell cycle regulation by activating the Akt and CDC2 kinases. RGC-32 is expressed by tumor cells and plays a dual role in cancer, functioning as either a tumor promoter by endorsing malignancy initiation, progression, invasion, metastasis, and angiogenesis, or as a tumor suppressor. In this review, we present recent data describing the versatile, multifaceted roles of C5b-9 and its effector, RGC-32, in cancer.

Indexed as

Disease SusceptibilityApoptosisCell Cycle ProteinsCell ProliferationComplement ActivationComplement Membrane Attack ComplexCytotoxicity, ImmunologicGene Expression Regulation, NeoplasticHumansMuscle ProteinsNeoplasmsNeovascularization, PathologicNerve Tissue ProteinsSignal TransductionTranscription, GeneticCell Cycle ProteinsComplement Membrane Attack ComplexMuscle ProteinsNerve Tissue ProteinsRGCC protein, humanapoptosisC5b-9cancercell proliferationRGC-32

Identifiers

PMID31156630
PMCPMC6530392
OpenAlexW2944792900

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.