Evidence map›Paper›PMID 36103091›Full record

ArticleCellular and molecular life sciences : CMLS2022

Metabolic reprogramming in the OPA1-deficient cells.

Wenting Dai, Zhichao Wang, Qiong A Wang, David Chan, Lei Jiang

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Wenting DaiDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, City of Hope National Medical Center, Duarte, CA, USA.
Zhichao WangDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, City of Hope National Medical Center, Duarte, CA, USA.
Qiong A WangDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, City of Hope National Medical Center, Duarte, CA, USA.
David ChanDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Lei JiangDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, City of Hope National Medical Center, Duarte, CA, USA. ljiang@coh.org.ORCID http://orcid.org/0000-0002-8596-556X
City Of Hope National Medical Center · USCalifornia Institute of Technology · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Homeostatic Mechanisms Regulating Mitochondrial Health EQUIPMENT SUPPLEMENTR35GM127147 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI David C Chan · 2018 to 2026
$6.0M
Characterization and functional assessment of a novel population of Wnt/beta-catenin driven adopocytes.R01DK128907 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, YIPING, WANG, QIONG ANNABEL · 2021 to 2024
$2.0M
Mammary Adipocyte Remodeling in Health and DiseaseR01HD096152 · NICHD · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WANG, QIONG ANNABEL · 2020 to 2024
$1.8M
Defining the Role of Adipogenesis in Age-Associated AdiposityR01AG063854 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WANG, QIONG ANNABEL · 2020 to 2024
$1.8M
American Diabetes Association Research Foundation 1-19-JDF-023City of Hope P30CA033572Foundation for the National Institutes of Health R01AG063854Foundation for the National Institutes of Health R01HD096152NCI NIH HHS P30 CA033572NIA NIH HHS R01 AG063854NICHD NIH HHS R01 HD096152NIDDK NIH HHS R01 DK128907NIGMS NIH HHS R35 GM127147NIH HHS R01DK128907
6 · The paper itself

Abstract

OPA1, a dynamin-related GTPase mutated in autosomal dominant optic atrophy, is essential for the fusion of the inner mitochondrial membrane. Although OPA1 deficiency leads to impaired mitochondrial morphology, the role of OPA1 in central carbon metabolism remains unclear. Here, we aim to explore the functional role and metabolic mechanism of OPA1 in cell fitness beyond the control of mitochondrial fusion. We applied [U-

Indexed as

GlutamineGTP PhosphohydrolasesAnimalsCitratesFibroblastsGlucoseMiceCitratesGlucoseGlutamineGTP PhosphohydrolasesOpa1 protein, mouseCell growthCitrateDe novo lipogenesisOPA1 dysfunctionOxidative metabolismReductive carboxylation

Identifiers

PMID36103091
PMCPMC11803027
OpenAlexW4295669235

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.