Evidence map›Paper›PMID 42244655›Full record

ArticlebioRxiv : the preprint server for biology2026

Cyclin D1 regulates the hepatic response to feeding: Evidence for non-cell cycle roles in the liver.

Heng Wu, Jonathan I Hauser, Na Yang, Nikolai Timchenko, Maggie Klaers, Rahagir Salekeen, Juan C Manivel, Juan E Abrahante, Linshan Laux, Matthew J Yousefzadeh and 9 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

19 authors.

Heng WuDivision of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, Minneapolis, MN 55455.
Jonathan I HauserMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.
Na YangLaboratory of Genetics and Genomics, National Institute on Aging, NIH, Baltimore, MD 21224.
Nikolai TimchenkoDepartment of Surgery, University of Cincinnati College of Medicine, Cincinnati, OH 45229.
Maggie KlaersMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.
Rahagir SalekeenMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.
Juan C ManivelDepartment of Pathology, Minneapolis VA Health Care System, Minneapolis, MN 55417.
Juan E AbrahanteMinnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN 55455.
Linshan LauxMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.
Matthew J YousefzadehMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.
Michael P SchonfeldDepartment of Internal Medicine, University of Kansas Medical Center, Kansas City, KS 66160.
Irina TikhanovichDepartment of Internal Medicine, University of Kansas Medical Center, Kansas City, KS 66160.
Sayeed IkramuddinDepartment of Surgery, University of Minnesota, Minneapolis, Minnesota, USA 55455.
Satdarshan S MongaOrgan Pathobiology and Therapeutics Institute and Pittsburgh Liver Research Center, University of Pittsburgh, Pittsburgh, PA 15261.
Oyedele A AdeyiDepartment of Pathology, Heersink School of Medicine, University of Alabama at Birmingham.
Laura J NiedernhoferMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.ORCID 0000-0002-1074-1385
Payel SenLaboratory of Genetics and Genomics, National Institute on Aging, NIH, Baltimore, MD 21224.
Matthew S GillMasonic Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455.
Jeffrey H AlbrechtDivision of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, Minneapolis, MN 55455.ORCID 0009-0002-6268-0315

Funding

Role of Wnt/Beta-Catenin Signaling in Liver DevelopmentR01DK062277 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Satdarshan Singh Monga · 2004 to 2026
$9.0M
The Cyclin D1/CDK4 Complex in Hepatocyte ProliferationR01DK054921 · NIDDK · UNIVERSITY OF MINNESOTA · PI ALBRECHT, JEFFREY H · 1998 to 2017
$4.5M
The role of DNAJB1-PKAc-β-catenin axis in fibrolamellar HCCR01CA278834 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI Soona Shin · 2023 to 2026
$2.5M
The role of H3K4 demethylases in alcohol-associated liver disease development and resolutionR01AA031270 · NIAAA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Irina Tikhanovich · 2024 to 2026
$1.5M
Vertical Sleeve Gastrectomy for Treatment of NASH: a pilot randomized controlR01DK128325 · NIDDK · UNIVERSITY OF MINNESOTA · PI HAMEED, BILAL, IKRAMUDDIN, SAYEED · 2021 to 2023
$947k
Hepatic Energy Fluxes, NASH, and Vertical Sleeve GastrectomyR21DK122832 · NIDDK · UNIVERSITY OF MINNESOTA · PI CRAWFORD, PETER A, IKRAMUDDIN, SAYEED · 2019 to 2020
$424k
NCI NIH HHS R01 CA278834NIAAA NIH HHS R01 AA031270NIDDK NIH HHS R01 DK054921NIDDK NIH HHS R01 DK062277NIDDK NIH HHS R01 DK128325NIDDK NIH HHS R21 DK122832
6 · The paper itself

Abstract

Objectives: Prior studies have shown that cyclin D1 regulates diverse aspects of liver metabolism during cell cycle progression. Interestingly, this protein is induced in hepatocytes by feeding, but its function in modulating hepatic postprandial physiology is poorly characterized. The aim of this study was to evaluate the contribution of cyclin D1 to the hepatic response to feeding and to gain insight into its potential non-proliferative roles in other conditions. Methods: Mice with or without hepatocyte cyclin D1 (D1 Results: Cyclin D1 regulated hepatic gene networks involved in glucose and lipid metabolism, protein synthesis, immune response, and other pathways after feeding. Induction of acute phase response proteins was markedly inhibited in D1 Conclusions: Cyclin D1 regulates nutrient-mediated physiology in the liver and

Indexed as

Acute-Phase ProteinsCEBPBChREBPLcn2NHR-49PAI-1Senescence-Associated Secretory Phenotype (SASP)

Identifiers

PMID42244655
PMCPMC13232279

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.