Evidence map›Paper›PMID 32851774›Full record

ArticleEMBO reports2020

MicroRNA-195 controls MICU1 expression and tumor growth in ovarian cancer.

Geeta Rao, Shailendra Kumar Dhar Dwivedi, Yushan Zhang, Anindya Dey, Khader Shameer, Ramachandran Karthik, Subramanya Srikantan, Md Nazir Hossen, Jonathan D Wren, Muniswamy Madesh and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Mitochondrial CaJournal of cellular physiology · 2025
    Review
  2. Article
  3. Review
  4. Article
  5. MICU1's calcium sensing beyond mitochondrial calcium uptake.Biochimica et biophysica acta. Molecular cell research · 2024
    Review
  6. Review
  7. Article
  8. Article
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  11. Review
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  15. IGF-1 boosts mitochondrial function by a CaFrontiers in physiology · 2023
    Article
  16. Annals of translational medicine · 2022
    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

13 authors at 4 institutions in 1 country.

Geeta Rao *Department of Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Shailendra Kumar Dhar Dwivedi *Department of Obstetrics and Gynecology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Yushan ZhangDepartment of Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Anindya DeyDepartment of Obstetrics and Gynecology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Khader ShameerInstitute of Next Generation Healthcare (INGH), Icahn Institute for Data Science and Genomic Technology, Department of Genetics and Genomic Sciences, Mount Sinai Health System, New York, NY, USA.
Ramachandran KarthikDepartment of Medicine, Cardiology Division, University of Texas Health San Antonio, San Antonio, TX, USA.
Subramanya SrikantanDepartment of Medicine, Cardiology Division, University of Texas Health San Antonio, San Antonio, TX, USA.
Md Nazir HossenDepartment of Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Jonathan D WrenGenes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.ORCID 0000-0003-2776-3545
Muniswamy MadeshDepartment of Medicine, Cardiology Division, University of Texas Health San Antonio, San Antonio, TX, USA.
Joel T DudleyInstitute of Next Generation Healthcare (INGH), Icahn Institute for Data Science and Genomic Technology, Department of Genetics and Genomic Sciences, Mount Sinai Health System, New York, NY, USA.
Resham BhattacharyaDepartment of Obstetrics and Gynecology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Priyabrata MukherjeeDepartment of Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.ORCID 0000-0002-0557-0833
University of Oklahoma Health Sciences Center · USThe University of Texas Health Science Center at San Antonio · USMount Sinai Health System · USOklahoma Medical Research Foundation · US

Funding

Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TIMOTHY M VANWAGONER · 2013 to 2026
$68.2M
Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Wade Williams · 2018 to 2026
$27.1M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
Mount Sinai Institutes for Clinical and Translational SciencesUL1TR000067 · NCATS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SAMPSON, HUGH A · 2012 to 2014
$16.5M
Molecular Mechanism of Antiangiogenic Properties of Gold NanoparticleR01CA136494 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI MUKHERJEE, PRIYABRATA · 2009 to 2020
$2.9M
Reprogramming Tumor Microenvironment by NanoparticleR01CA213278 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI MUKHERJEE, PRIYABRATA · 2017 to 2021
$1.7M
Exploiting gold nanoparticle as a probe to identify therapeutic targetsR01CA260449 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Resham Bhattacharya, Priyabrata Mukherjee · 2022 to 2026
$1.6M
Role of miR-195 in Chemo-Resistant Ovarian CancerR21CA280507 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DWIVEDI, SHAILENDRA KUMAR DHAR · 2023 to 2023
$169k
NCATS NIH HHS UL1 TR000067NCI NIH HHS P30 CA225520NCI NIH HHS R01 CA136494NCI NIH HHS R01 CA213278NCI NIH HHS R01 CA260449NCI NIH HHS R21 CA280507NIGMS NIH HHS P20 GM103639NIGMS NIH HHS U54 GM104938
6 · The paper itself

Abstract

MICU1 is a mitochondrial inner membrane protein that inhibits mitochondrial calcium entry; elevated MICU1 expression is characteristic of many cancers, including ovarian cancer. MICU1 induces both glycolysis and chemoresistance and is associated with poor clinical outcomes. However, there are currently no available interventions to normalize aberrant MICU1 expression. Here, we demonstrate that microRNA-195-5p (miR-195) directly targets the 3' UTR of the MICU1 mRNA and represses MICU1 expression. Additionally, miR-195 is under-expressed in ovarian cancer cell lines, and restoring miR-195 expression reestablishes native MICU1 levels and the associated phenotypes. Stable expression of miR-195 in a human xenograft model of ovarian cancer significantly reduces tumor growth, increases tumor doubling times, and enhances overall survival. In conclusion, miR-195 controls MICU1 levels in ovarian cancer and could be exploited to normalize aberrant MICU1 expression, thus reversing both glycolysis and chemoresistance and consequently improving patient outcomes.

Indexed as

Cation Transport ProteinsMicroRNAsOvarian NeoplasmsCalcium-Binding ProteinsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGlycolysisHumansMitochondrial Membrane Transport ProteinsCalcium-Binding ProteinsCation Transport ProteinsMicroRNAsMICU1 protein, humanMIRN195 microRNA, humanMitochondrial Membrane Transport ProteinschemoresistanceglycolysisMICU1/CBARA1miR-195Ovarian cancer

Identifiers

PMID32851774
PMCPMC7534609
OpenAlexW3081304973

What OpenQuestion holds

Textmetadata
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.