Evidence map›Paper›PMID 30389917›Full record

ArticleNature communications2018

Exosomes derived from HIV-1-infected cells promote growth and progression of cancer via HIV TAR RNA.

Lechuang Chen, Zhimin Feng, Hong Yue, Douglas Bazdar, Uri Mbonye, Chad Zender, Clifford V Harding, Leslie Bruggeman, Jonathan Karn, Scott F Sieg and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
4.1field-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

62 citing papers in PubMed, 92 citations in OpenAlex.

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2 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

12 authors at 3 institutions in 1 country.

Lechuang ChenDepartment of Biological Sciences, Case Western Reserve University School of Dental Medicine, Cleveland, OH, 44106, USA.
Zhimin FengDepartment of Biological Sciences, Case Western Reserve University School of Dental Medicine, Cleveland, OH, 44106, USA.
Hong YueDepartment of Biological Sciences, Case Western Reserve University School of Dental Medicine, Cleveland, OH, 44106, USA.
Douglas BazdarDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.
Uri MbonyeDepartment of Molecular Biology & Microbiology, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.
Chad ZenderDepartment of Otolaryngology/ENT Institute, Case Western Reserve University School of Medicine and University Hospitals Cleveland Medical Center, Cleveland, OH, 44106, USA.
Clifford V HardingCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, 44106, USA.ORCID http://orcid.org/0000-0002-6333-162X
Leslie BruggemanCenter for AIDS Research, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, OH, 44106, USA.ORCID http://orcid.org/0000-0001-5874-705X
Jonathan KarnDepartment of Molecular Biology & Microbiology, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.ORCID http://orcid.org/0000-0002-2900-094X
Scott F SiegDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.ORCID http://orcid.org/0000-0002-1769-8682
Bingcheng WangCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, 44106, USA.
Ge JinDepartment of Biological Sciences, Case Western Reserve University School of Dental Medicine, Cleveland, OH, 44106, USA. ge.jin@case.edu.ORCID http://orcid.org/0000-0002-9508-9698
University Hospitals of Cleveland · USUniversity School · USCase Western Reserve University · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
AIDS and Cancer Specimen Resource (ACSR)UM1CA181255 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jeffrey Michael Bethony, Anna Coghill · 2013 to 2026
$56.7M
WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Sharon L. Hillier, JONATHAN KARN · 1994 to 2026
$50.0M
Targeting EphA2 in GlioblastomaR01NS096956 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2016 to 2021
$2.6M
Head Neck Cancer, beta-defensins, and immune responsesR01DE025284 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI JIN, GE · 2015 to 2019
$2.0M
Oral immune plasticity, HIV-infected T cell extracellular vesicles, and oral cancerR01DE026925 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI JIN, GE · 2017 to 2021
$1.9M
EphA2 kinase in prostate cancerR01CA155676 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2011 to 2016
$1.6M
NCI NIH HHS P30 CA043703NCI NIH HHS R01 CA155676NCI NIH HHS UM1 CA181255NIAID NIH HHS P30 AI036219NIDCR NIH HHS R01 DE025284NIDCR NIH HHS R01 DE026925NINDS NIH HHS R01 NS096956
6 · The paper itself

Abstract

People living with HIV/AIDS on antiretroviral therapy have increased risk of non-AIDS-defining cancers (NADCs). However, the underlying mechanism for development and progression of certain NADCs remains obscure. Here we show that exosomes released from HIV-infected T cells and those purified from blood of HIV-positive patients stimulate proliferation, migration and invasion of oral/oropharyngeal and lung cancer cells. The HIV transactivation response (TAR) element RNA in HIV-infected T-cell exosomes is responsible for promoting cancer cell proliferation and inducing expression of proto-oncogenes and Toll-like receptor 3 (TLR3)-inducible genes. These effects depend on the loop/bulge region of the molecule. HIV-infected T-cell exosomes rapidly enter recipient cells through epidermal growth factor receptor (EGFR) and stimulate ERK1/2 phosphorylation via the EGFR/TLR3 axis. Thus, our findings indicate that TAR RNA-containing exosomes from HIV-infected T cells promote growth and progression of particular NADCs through activation of the ERK cascade in an EGFR/TLR3-dependent manner.

Indexed as

Disease ProgressionAnimalsCell Line, TumorCell MovementCell ProliferationErbB ReceptorsExosomesGene Expression RegulationHEK293 CellsHIV-1HIV InfectionsHIV Long Terminal RepeatHumansMAP Kinase Signaling SystemMice, NudeNeoplasmsErbB ReceptorsToll-Like Receptor 3

Identifiers

PMID30389917
PMCPMC6214989
OpenAlexW2899041727

What OpenQuestion holds

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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.