Evidence map›Paper›PMID 41362097›Full record

ReviewFEBS letters2026

Integration of circadian and hypoxia signaling via non-canonical heterodimerization.

Sicong Wang, Katja A Lamia

Abstract readReview
In one paragraph

Review in FEBS letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

2 authors.

Sicong WangDepartment of Molecular and Cellular Biology, Scripps Research, 10550 N Torrey Pines Road, MB-21, La Jolla, CA, 92037, USA.
Katja A LamiaDepartment of Molecular and Cellular Biology, Scripps Research, 10550 N Torrey Pines Road, MB-21, La Jolla, CA, 92037, USA.ORCID 0000-0001-9533-0499

Funding

Impacting Cell Growth through altered circadian proteolysisR01CA211187 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI Katja A Lamia · 2017 to 2026
$4.6M
Establishing a mechanistic basis for enhanced tumorigenesis under chronic circadian disruptionR01CA271500 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI Katja A Lamia · 2023 to 2026
$2.4M
NCI NIH HHS R01 CA211187NCI NIH HHS R01 CA271500
6 · The paper itself

Abstract

CLOCK, BMAL1, and HIFs are basic helix-loop-helix and Per-Arnt-Sim domain (bHLH-PAS) proteins, which function as transcription factors. bHLH-PAS proteins are designated in two classes. Many class I proteins are regulated by environmental signals via their PAS domains, but such signals have not been identified for all. Class II (ARNTs and BMALs) are partners for Class I and can be regulated by synthetic PAS ligands. Previous studies suggested restricted dimerization for bHLH-PAS proteins. BMAL1 and BMAL2 were believed to dimerize only with CLOCK and NPAS2, while ARNT was thought to dimerize with most Class I proteins except for CLOCK and NPAS2. The logic underlying these assumptions was flawed, and evidence supports dimerization of both HIF1α and HIF2α with BMAL1.

Indexed as

Circadian RhythmHypoxiaProtein MultimerizationSignal TransductionAnimalsARNTL Transcription FactorsAryl Hydrocarbon Receptor Nuclear TranslocatorBasic Helix-Loop-Helix ProteinsCLOCK ProteinsHumansHypoxia-Inducible Factor 1, alpha SubunitARNTL Transcription FactorsAryl Hydrocarbon Receptor Nuclear TranslocatorBasic Helix-Loop-Helix ProteinsCLOCK ProteinsHypoxia-Inducible Factor 1, alpha Subunit

Identifiers

PMID41362097
PMCPMC13022751

What OpenQuestion holds

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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.