Evidence map›Paper›PMID 36595688›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Hepatic SEL1L-HRD1 ER-associated degradation regulates systemic iron homeostasis via ceruloplasmin.

Pattaraporn Thepsuwan, Asmita Bhattacharya, Zhenfeng Song, Stephen Hippleheuser, Shaobin Feng, Xiaoqiong Wei, Nupur K Das, Mariana Sierra, Juncheng Wei, Deyu Fang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  5. SEL1L-HRD1-mediated ERAD in mammals.Nature cell biology · 2025
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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 3 institutions in 1 country.

Pattaraporn ThepsuwanCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.
Asmita BhattacharyaDepartment of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105.ORCID 0000-0002-5669-8036
Zhenfeng SongCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.
Stephen HippleheuserCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.
Shaobin FengCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.
Xiaoqiong WeiDepartment of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105.ORCID 0000-0001-7576-4820
Nupur K DasDepartment of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105.ORCID 0000-0002-5652-1134
Mariana SierraDepartment of Physics and Astronomy, Wayne State University, Detroit, MI 48201.
Juncheng WeiDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.
Deyu FangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.
Yu-Ming M HuangDepartment of Physics and Astronomy, Wayne State University, Detroit, MI 48201.
Kezhong ZhangCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.ORCID 0000-0002-6062-235X
Yatrik M ShahDepartment of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105.
Shengyi SunCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.ORCID 0000-0002-1734-3902
Wayne State University · USUniversity of Michigan · USNorthwestern University · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Control of iron absorption by intestinal HIF2 in iron and hematological disordersR01DK095201 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAH, YATRIK M · 2012 to 2025
$5.7M
The role of HIF2alpha in colon carcinogenesisR01CA148828 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAH, YATRIK M · 2010 to 2025
$5.2M
Regulation of Hepatic Steatosis by an ER Stress-Inducible Transcription Factor CRR01DK090313 · NIDDK · WAYNE STATE UNIVERSITY · PI Kezhong Zhang · 2011 to 2026
$5.0M
Novel Role of Hepatic SEL1L-HRD1 ERAD in FGF21 Gene TranscriptionR01DK120330 · NIDDK · UNIVERSITY OF VIRGINIA · PI Deyu Fang, Ling Qi · 2018 to 2026
$4.9M
A deubiquitination module controls Treg adaptation to tumor microenvironmentR01CA257520 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU, ZHANG, BIN · 2021 to 2025
$2.8M
Understanding the mechanisms of iron addiction in colon cancerR01CA245546 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAH, YATRIK M · 2020 to 2024
$2.3M
Regulation of Rhythmic m6A RNA Modification by ER‐associated DegradationR01DK126908 · NIDDK · WAYNE STATE UNIVERSITY · PI FANG, DEYU, ZHANG, KEZHONG · 2021 to 2024
$2.2M
Novel role of endoplasmic reticulum-associated degradation in iron metabolismR01DK128077 · NIDDK · WAYNE STATE UNIVERSITY · PI Shengyi Sun · 2022 to 2026
$1.9M
Targeting a Treg deubiquitinase in antitumor immune therapyR01CA232347 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU · 2018 to 2022
$1.7M
Mitochondrial NAD kinase: function and mechanism in metabolismR01DK132065 · NIDDK · WAYNE STATE UNIVERSITY · PI ZHANG, KEZHONG, ZHANG, REN · 2022 to 2025
$1.5M
NCI NIH HHS R01 CA148828NCI NIH HHS R01 CA232347NCI NIH HHS R01 CA245546NCI NIH HHS R01 CA257520NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK090313NIDDK NIH HHS R01 DK095201NIDDK NIH HHS R01 DK120330NIDDK NIH HHS R01 DK126908NIDDK NIH HHS R01 DK128077
6 · The paper itself

Abstract

Iron homeostasis is critical for cellular and organismal function and is tightly regulated to prevent toxicity or anemia due to iron excess or deficiency, respectively. However, subcellular regulatory mechanisms of iron remain largely unexplored. Here, we report that SEL1L-HRD1 protein complex of endoplasmic reticulum (ER)-associated degradation (ERAD) in hepatocytes controls systemic iron homeostasis in a ceruloplasmin (CP)-dependent, and ER stress-independent, manner. Mice with hepatocyte-specific

Indexed as

CeruloplasminEndoplasmic Reticulum-Associated DegradationAnimalsEndoplasmic ReticulumHomeostasisIronMiceProteinsUbiquitin-Protein LigasesCeruloplasminIronProteinsUbiquitin-Protein Ligasesceruloplasminhepatocytesiron metabolismSEL1L-HRD1 ERAD

Identifiers

PMID36595688
PMCPMC9926173
OpenAlexW4313527901

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.