Evidence map›Paper›PMID 27932791›Full record

ArticleExperimental & molecular medicine2016

Migration and invasion of drug-resistant lung adenocarcinoma cells are dependent on mitochondrial activity.

Ji Hoon Jeon, Dong Keon Kim, Youngmi Shin, Hee Yeon Kim, Bomin Song, Eun Young Lee, Jong Kwang Kim, Hye Jin You, Heesun Cheong, Dong Hoon Shin and 4 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 66 citations in OpenAlex.

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  16. Quantitative analysis of mitochondrial membrane potential heterogeneity in unsynchronized and synchronized cancer cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
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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

14 authors at 2 institutions in 1 country.

Ji Hoon JeonResearch Institute, National Cancer Center, Goyang, Korea.
Dong Keon KimResearch Institute, National Cancer Center, Goyang, Korea.
Youngmi ShinResearch Institute, National Cancer Center, Goyang, Korea.
Hee Yeon KimResearch Institute, National Cancer Center, Goyang, Korea.
Bomin SongResearch Institute, National Cancer Center, Goyang, Korea.
Eun Young LeeResearch Institute, National Cancer Center, Goyang, Korea.
Jong Kwang KimResearch Institute, National Cancer Center, Goyang, Korea.
Hye Jin YouResearch Institute, National Cancer Center, Goyang, Korea.
Heesun CheongResearch Institute, National Cancer Center, Goyang, Korea.
Dong Hoon ShinResearch Institute, National Cancer Center, Goyang, Korea.
Seong-Tae KimDepartment of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Korea.
Jae-Ho CheongDepartment of Surgery, Yonsei University College of Medicine, Seoul, Korea.
Soo Youl KimResearch Institute, National Cancer Center, Goyang, Korea.
Hyonchol JangResearch Institute, National Cancer Center, Goyang, Korea.ORCID 0000-0003-1436-457X
National Cancer Center · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A small proportion of cancer cells have stem-cell-like properties, are resistant to standard therapy and are associated with a poor prognosis. The metabolism of such drug-resistant cells differs from that of nearby non-resistant cells. In this study, the metabolism of drug-resistant lung adenocarcinoma cells was investigated. The expression of genes associated with oxidative phosphorylation in the mitochondrial membrane was negatively correlated with the prognosis of lung adenocarcinoma. Because the mitochondrial membrane potential (MMP) reflects the functional status of mitochondria and metastasis is the principal cause of death due to cancer, the relationship between MMP and metastasis was evaluated. Cells with a higher MMP exhibited greater migration and invasion than those with a lower MMP. Cells that survived treatment with cisplatin, a standard chemotherapeutic drug for lung adenocarcinoma, exhibited increased MMP and enhanced migration and invasion compared with parental cells. Consistent with these findings, inhibition of mitochondrial activity significantly impeded the migration and invasion of cisplatin-resistant cells. RNA-sequencing analysis indicated that the expression of mitochondrial complex genes was upregulated in cisplatin-resistant cells. These results suggested that drug-resistant cells have a greater MMP and that inhibition of mitochondrial activity could be used to prevent metastasis of drug-resistant lung adenocarcinoma cells.

Indexed as

Drug Resistance, NeoplasmAdenocarcinomaAdenocarcinoma of LungAntineoplastic AgentsCell Line, TumorCell MovementCisplatinGene Expression Regulation, NeoplasticHumansLung NeoplasmsMitochondriaNeoplasm InvasivenessPrognosisAntineoplastic AgentsCisplatin

Identifiers

PMID27932791
PMCPMC5192074
OpenAlexW2560535385

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.