Evidence map›Paper›PMID 22505650›Full record

ArticleCancer research2012

Cell-mediated autophagy promotes cancer cell survival.

William J Buchser, Thomas C Laskow, Philip J Pavlik, Hui-Min Lin, Michael T Lotze

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

82 citing papers in PubMed, 138 citations in OpenAlex.

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  16. Insight into autophagy in platinum resistance of cancer.International journal of clinical oncology · 2023
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22 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

5 authors at 1 institution in 1 country.

William J BuchserDepartment of Surgery, Graduate School of Public Health, University of Pittsburgh and Biostatistics Facility, University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania 15232, USA.
Thomas C Laskow
Philip J Pavlik
Hui-Min Lin
Michael T Lotze
UPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
PROTEOMICS COREP01CA101944 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LOTZE, MICHAEL T · 2005 to 2009
$8.5M
NCATS NIH HHS UL1 TR000005NCI NIH HHS 1 P01 CA 101944-04NCI NIH HHS 5P30 CA47904NCI NIH HHS P01 CA101944NCI NIH HHS P30 CA047904
6 · The paper itself

Abstract

Immune effector cells integrate signals that define the nature and magnitude of the subsequent response. Experimental measures for immune cell-mediated lysis of tumors or virally infected targets rely on average responses of permeability or apoptotic changes within a population of targets. Here, we examined individual target cells following interaction with lymphoid effectors. We found that human peripheral blood lymphocytes not only provide lytic signals but also promote autophagy in the remaining cells. At high effector-to-target ratios, autophagy was induced in several human tumors, as assessed by induction of LC3 puncta and diminished p62. Natural killer cells are a primary mediator of this process. In addition, target cell autophagy was enhanced by provision of interleukin (IL)-2, whereas IL-10 attenuated this effect, and cell-to-cell contact strongly enhanced lymphocyte-mediated autophagy. Although IFN-γ can induce autophagy in target cells, IFN-α acted directly on the targets or in concert with lymphocytes to diminish target autophagy in some cell types. Importantly, cell-mediated autophagy promoted resistance from treatment modalities designed to eradicate tumor cells. Our findings therefore show that the lymphocyte-induced cell-mediated autophagy promotes cancer cell survival and may represent an important target for development of novel therapies.

Indexed as

AutophagyCytotoxicity, ImmunologicAdaptor Proteins, Signal TransducingCell CommunicationCell Line, TumorCell SurvivalColonic NeoplasmsHumansInterferon-alphaInterferon-gammaInterleukin-10Interleukin-2Killer Cells, NaturalLeukocytes, MononuclearMicrotubule-Associated ProteinsPancreatic NeoplasmsAdaptor Proteins, Signal TransducingInterferon-alphaInterferon-gammaInterleukin-10Interleukin-2MAP1LC3A protein, humanMicrotubule-Associated ProteinsSequestosome-1 ProteinSQSTM1 protein, human

Identifiers

PMID22505650
PMCPMC3505669
OpenAlexW2157429299

What OpenQuestion holds

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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.