Evidence map›Paper›PMID 28283188›Full record

ArticleMutation research2017

Targeted cytoplasmic irradiation and autophagy.

Jinhua Wu, Bo Zhang, Yen-Ruh Wuu, Mercy M Davidson, Tom K Hei

Open access · greenAbstract read
In one paragraph

Article in Mutation research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Low-Dose Non-Targeted Effects and Mitochondrial Control.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Medicinal Thiols: Current Status and New Perspectives.Mini reviews in medicinal chemistry · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Focus small to find big - the microbeam story.International journal of radiation biology · 2018
    Review
  13. Article
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 2 countries.

Jinhua WuCenter for Radiological Research, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, VC 11-205, New York, N.Y., United States; Institute of Plasma Physics, Chinese Academy of Sciences, Hefei, Anhui, 230031, China.
Bo ZhangCenter for Radiological Research, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, VC 11-205, New York, N.Y., United States.
Yen-Ruh WuuCenter for Radiological Research, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, VC 11-205, New York, N.Y., United States.
Mercy M DavidsonDepartment of Radiation Oncology, Columbia University, 630 West 168th Street, P&S 11-451, New York, N.Y., 10032, United States.
Tom K HeiCenter for Radiological Research, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, VC 11-205, New York, N.Y., United States. Electronic address: tkh1@cumc.columbia.edu.
Columbia University · US

Funding

THE FUNCTIONAL GENOMICS OF BYSTANDER RESPONSESP01CA049062 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HEI, TOM K. · 1990 to 2014
$21.9M
TR&D 3P41EB002033 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BRENNER, DAVID JONATHAN · 2003 to 2018
$17.0M
Cytoplasmic Damage and GenotoxicityR01ES012888 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HEI, TOM K. · 2004 to 2016
$3.9M
NCI NIH HHS P01 CA049062NIBIB NIH HHS P41 EB002033NIEHS NIH HHS R01 ES012888
6 · The paper itself

Abstract

The effect of ionizing irradiation on cytoplasmic organelles is often underestimated because the general dogma considers direct DNA damage in the nuclei to be the primary cause of radiation induced toxicity. Using a precision microbeam irradiator, we examined the changes in mitochondrial dynamics and functions triggered by targeted cytoplasmic irradiation with α-particles. Mitochondrial dysfunction induced by targeted cytoplasmic irradiation led to activation of autophagy, which degraded dysfunctional mitochondria in order to maintain cellular energy homeostasis. The activation of autophagy was cytoplasmic irradiation-specific and was not detected in nuclear irradiated cells. This autophagic process was oxyradical-dependent and required the activity of the mitochondrial fission protein dynamin related protein 1 (DRP1). The resultant mitochondrial fission induced phosphorylation of AMP activated protein kinase (AMPK) which leads to further activation of the extracellular signal-related kinase (ERK) 1/2 with concomitant inhibition of the mammalian target of rapamycin (mTOR) to initiate autophagy. Inhibition of autophagy resulted in delayed DNA damage repair and decreased cell viability, which supports the cytoprotective function of autophagy. Our results reveal a novel mechanism in which dysfunctional mitochondria are degraded by autophagy in an attempt to protect cells from toxic effects of targeted cytoplasmic radiation.

Indexed as

Alpha ParticlesApoptosisAutophagyCells, CulturedCytoplasmEpithelial CellsHumansMitochondrial DynamicsReactive Oxygen SpeciesRespiratory SystemTOR Serine-Threonine KinasesMTOR protein, humanReactive Oxygen SpeciesTOR Serine-Threonine KinasesAMPKAutophagyCytoplasmic irradiationDRP1Mitochondria dysfunctionMitophagy

Identifiers

PMID28283188
PMCPMC5581273
OpenAlexW2592745032

What OpenQuestion holds

Textmetadata
LicenceTDM
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.