Evidence map›Paper›PMID 34189138›Full record

ArticleBioMed research international2021

MCU That Is Transcriptionally Regulated by Nrf2 Augments Malignant Biological Behaviors in Oral Squamous Cell Carcinoma Cells.

Ran Wu, Weiwen Zuo, Xiaoliang Xu, Lei Bi, Chunguang Zhang, Hui Chen, Hui Liu

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  6. The mitochondrial CabioRxiv : the preprint server for biology · 2023
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  7. The mitochondrial CaFrontiers in cell and developmental biology · 2023
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  8. Review
  9. Review
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Ran WuDepartment of Stomatology, North China University of Science and Technology Affiliated Hospital, Tangshan, 063000 Hebei, China.ORCID https://orcid.org/0000-0003-4048-5551
Weiwen ZuoDepartment of Stomatology, Tangshan Vocational and Technical College, Tangshan, 063000 Hebei, China.
Xiaoliang XuDepartment of Stomatology, The Second Hospital of Tangshan, Tangshan, 063000 Hebei, China.
Lei BiDepartment of Stomatology, North China University of Science and Technology Affiliated Hospital, Tangshan, 063000 Hebei, China.
Chunguang ZhangDepartment of Stomatology, North China University of Science and Technology Affiliated Hospital, Tangshan, 063000 Hebei, China.
Hui ChenDepartment of Stomatology, North China University of Science and Technology Affiliated Hospital, Tangshan, 063000 Hebei, China.
Hui LiuDepartment of Stomatology, North China University of Science and Technology Affiliated Hospital, Tangshan, 063000 Hebei, China.ORCID https://orcid.org/0000-0002-8876-7622
North China University of Science and Technology Affiliated Hospital · CNSecond Hospital of Tangshan · CNTangshan College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo clarify the role and molecular mechanism of mitochondrial calcium uniporter (MCU) in the malignant biological behaviors of oral squamous cell carcinoma (OSCC) cells through clinical and cellular experiments.

methodsImmunohistochemistry and qRT-PCR techniques were used to observe the expression of MCU, nuclear factor erythroid 2-related factor 2 (Nrf2), mitochondrial calcium uptake 1 (MICU1), and MICU2 in OSCC and normal tissues. After treatment with si-MCU, spermine, and/or sh-Nrf2, malignant biological behaviors of OSCC cells including proliferation, migration, and apoptosis were detected by clone formation, migration, and mitochondrial membrane potential (MMP) assays. Furthermore, MCU, MICU1, MICU2, Nrf2, and other proteins related to malignant biological behaviors were examined using western blot, immunohistochemistry, and immunofluorescence assays.

resultsMCU, Nrf2, and MICU1 were strongly expressed in OSCC as compared to normal tissues, while MICU2 was relatively weakly expressed in OSCC tissues. Knockdown of MCU distinctly weakened proliferation and migration and lowered MMP level in CAL 27 cells. Conversely, its activation reinforced migrated capacity and increased MMP level in CAL 27 cells, which was reversed after cotransfection with sh-Nrf2. After treatment with si-MCU or spermine, Nrf2 expression was not affected in CAL 27 cells. However, MCU expression was distinctly suppressed in CAL 27 cells transfected with sh-Nrf2. Furthermore, knockdown of Nrf2 significantly reversed the increase in expression of MICU1 and MICU2 induced by MCU activation in CAL 27 cells.

conclusionMCU, as a novel oncogene of OSCC, augments malignant biological behaviors of OSCC cells, which could be transcriptionally regulated by Nrf2.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisCalcium ChannelsCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationHumansMembrane Potential, MitochondrialMitochondrial Membrane Transport ProteinsMouth NeoplasmsNF-E2-Related Factor 2PhenotypeSpermineSquamous Cell Carcinoma of Head and NeckCalcium Channelsmitochondrial calcium uniporterMitochondrial Membrane Transport ProteinsNFE2L2 protein, humanNF-E2-Related Factor 2Spermine

Identifiers

PMID34189138
PMCPMC8195654
OpenAlexW3167752044

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.