Evidence map›Paper›PMID 33264641›Full record

ReviewCancer letters2021

FGF21 in obesity and cancer: New insights.

Weiqin Lu, Xiaokun Li, Yongde Luo

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

54 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Cross-Species Upregulation ofCurrent issues in molecular biology · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Circulating Inflammation Biomarkers and the Risk of Esophageal Adenocarcinoma: A Nested Case-Control Study in the Department of Defense Serum Repository.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Article
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

3 authors at 2 institutions in 2 countries.

Weiqin LuDivision of Gastroenterology and Hepatology, Department of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA. Electronic address: weiqin.lu@stonybrookmedicine.edu.
Xiaokun LiSchool of Pharmaceutical Science, Wenzhou Medical University, China; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China. Electronic address: xiaokunli@wmu.edu.cn.
Yongde LuoDivision of Gastroenterology and Hepatology, Department of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA; School of Pharmaceutical Science, Wenzhou Medical University, China; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China; Centeer BioTherapeutics Ltd Co, Houston, TX, 77030, USA. Electronic address: yluo99@centeerbiotherapeutics.com.
Wenzhou Medical University · CNStony Brook Medicine · US

Funding

Targeting NADPH Oxidase for Pancreatic Cancer Prevention and TherapyR01CA240818 · NCI · UNIVERSITY OF TEXAS EL PASO · PI LU, WEIQIN · 2020 to 2024
$1.7M
Unraveling the Role of NADPH Oxidase in Inflammation-associated Pancreatic DiseasesR01DK123079 · NIDDK · UNIVERSITY OF TEXAS EL PASO · PI LU, WEIQIN · 2020 to 2024
$1.4M
Unraveling the Role of NADPH Oxidase in Inflammation-associated Pancreatic DiseasesR56DK123079 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI LU, WEIQIN · 2019 to 2019
$336k
NCI NIH HHS R01 CA240818NIDDK NIH HHS R01 DK123079NIDDK NIH HHS R56 DK123079
6 · The paper itself

Abstract

The endocrine FGF21 was discovered as a novel metabolic regulator in 2005 with new functions bifurcating from the canonic heparin-binding FGFs that directly promote cell proliferation and growth independent of a co-receptor. Early studies have demonstrated that FGF21 is a stress sensor in the liver and possibly, several other endocrine and metabolic tissues. Hepatic FGF21 signals via endocrine routes to quench episodes of metabolic derangements, promoting metabolic homeostasis. The convergence of mouse and human studies shows that FGF21 promotes lipid catabolism, including lipolysis, fatty acid oxidation, mitochondrial oxidative activity, and thermogenic energy dissipation, rather than directly regulating insulin and appetite. The white and brown adipose tissues and, to some extent, the hypothalamus, all of which host a transmembrane receptor binary complex of FGFR1 and co-receptor KLB, are considered the essential tissue and molecular targets of hepatic or pharmacological FGF21. On the other hand, a growing body of work has revealed that pancreatic acinar cells form a constitutive high-production site for FGF21, which then acts in an autocrine or paracrine mode. Beyond regulation of macronutrient metabolism and physiological energy expenditure, FGF21 appears to function in forestalling the development of fatty pancreas, steato-pancreatitis, fatty liver, and steato-hepatitis, thereby preventing the development of advanced pathologies such as pancreatic ductal adenocarcinoma or hepatocellular carcinoma. This review is intended to provide updates on these new discoveries that illuminate the protective roles of FGF21-FGFR1-KLB signal pathway in metabolic anomalies-associated severe tissue damage and malignancy, and to inform potential new preventive or therapeutic strategies for obesity-inflicted cancer patients via reducing metabolic risks and inflammation.

Indexed as

Adipose TissueAnimalsAutocrine CommunicationCarcinoma, HepatocellularCarcinoma, Pancreatic DuctalCell ProliferationDisease Models, AnimalEnergy MetabolismFatty LiverFibroblast Growth FactorsHumansHypothalamusKlotho ProteinsLipid MetabolismLiverLiver Neoplasmsfibroblast growth factor 21Fibroblast Growth FactorsKLB protein, humanKlb protein, mouseKlotho ProteinsMembrane ProteinsReceptor, Fibroblast Growth Factor, Type 1Hepatocellular carcinomaInflammationObesityOncogenic KRASPancreatic cancer

Identifiers

PMID33264641
PMCPMC7779663
OpenAlexW3107852906

What OpenQuestion holds

Textmetadata
LicenceTDM
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.