Evidence map›Paper›PMID 26867977›Full record

ArticleScientific reports2016

Hypoxia-mediated autophagic flux inhibits silver nanoparticle-triggered apoptosis in human lung cancer cells.

Jae-Kyo Jeong, Sangiliyandi Gurunathan, Min-Hee Kang, Jae Woong Han, Joydeep Das, Yun-Jung Choi, Deug-Nam Kwon, Ssang-Goo Cho, Chankyu Park, Han Geuk Seo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 103 citations in OpenAlex.

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  12. Sirtuins and Hypoxia in EMT Control.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  13. Review
  14. Review
  15. Facile In-Situ Fabrication of a Ternary ZnO/TiOAntibiotics (Basel, Switzerland) · 2021
    Article
  16. Article
  17. Review
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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 1 institution in 1 country.

Jae-Kyo JeongDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Sangiliyandi GurunathanDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Min-Hee KangDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Jae Woong HanDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Joydeep DasDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Yun-Jung ChoiDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Deug-Nam KwonDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Ssang-Goo ChoDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Chankyu ParkDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Han Geuk SeoDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Hyuk SongDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Jin-Hoi KimDepartment of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Konkuk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid tumors are frequently associated with resistance to chemotherapy because the fraction of hypoxic tumor cells is substantial. To understand the underlying mechanism of hypoxia on silver nanoparticle (AgNPs)-induced apoptosis, the expression of hypoxia-inducible factor (HIF)-1α, a hallmark of hypoxia, was measured in the presence and absence of AgNPs. The results showed that HIF-1α expression was upregulated after AgNPs treatment under both hypoxic and normoxic conditions. Cell viability assays showed that AgNPs promoted cell death in cancer cells but not in non-cancer cells, as cancer cells are slightly more acidic than normal cells. However, reactive oxygen species generation induced by AgNPs in lung cancer cells caused high susceptibility to oxidative stress, whereas pre-exposure to hypoxia blocked AgNPs-induced oxidative stress. Notably, HIF-1α inhibited AgNPs-induced mitochondria-mediated apoptosis by regulating autophagic flux through the regulation of ATG5, LC3-II, and p62. Further, cell viability after treatment of cancer cells with AgNPs under hypoxic conditions was lower in HIF-1α siRNA-transfected cells than in control siRNA-transfected cells, indicating that HIF-1α knockdown enhances hypoxia induced decrease in cell viability. Our results suggest that hypoxia-mediated autophagy may be a mechanism for the resistance of AgNPs-induced apoptosis and that strategies targeting HIF-1α may be used for cancer therapy.

Indexed as

ApoptosisAutophagyCell HypoxiaAntineoplastic AgentsCell Line, TumorCell SurvivalDrug ResistanceGene Expression ProfilingHumansHypoxia-Inducible Factor 1, alpha SubunitLung NeoplasmsNanoparticlesSilverAntineoplastic AgentsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitSilver

Identifiers

PMID26867977
PMCPMC4751501
OpenAlexW2411099800

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.