Evidence map›Paper›PMID 41573204›Full record

ArticleFrontiers in endocrinology2025

Stc2a inhibits IGF-stimulated somatic growth in favor of organismal survival under hypoxic stress.

Zhengyi Wang, Jinay Shah, Shuang Li, Shriya Jaggi, Hui Xu, Cunming Duan

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Zhengyi Wang *Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
Jinay Shah *Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
Shuang LiDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
Shriya JaggiDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
Hui XuDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
Cunming DuanDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In response to hypoxia, animals reduce somatic growth to shift energy resources toward the maintenance of vital functions and organismal survival. Although this phenomenon is widespread, the systemic factors and mechanisms involved remain poorly understood. Here we report that hypoxia causes major changes in zebrafish transcriptomic landscapes with hormonal activity or hormonal signaling identified as most prominently up-regulated GO term and KEGG pathway. Among the top in this group is Stanniocalcin 2a (Stc2a), a secreted glycoprotein that inhibits insulin-like growth factor (IGF) signaling by binding to pappalysin metalloproteinases and inhibiting their activities. The hypoxic induction of

Indexed as

GlycoproteinsHypoxiaInsulin-Like PeptidesIntercellular Signaling Peptides and ProteinsSomatomedinsStress, PhysiologicalZebrafishZebrafish ProteinsAnimalsSignal TransductionGlycoproteinsInsulin-Like PeptidesIntercellular Signaling Peptides and ProteinsSomatomedinsteleocalcinZebrafish Proteinshypoxia-inducible factorIGF1 receptorinsulin-like growth factorPAPP-Astanniocalcin 2zebrafish

Identifiers

PMID41573204
PMCPMC12819173

What OpenQuestion holds

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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.