Evidence map›Paper›PMID 32466971›Full record

ReviewSeminars in cell & developmental biology2021

Cilia signaling and obesity.

Staci E Engle, Ruchi Bansal, Patrick J Antonellis, Nicolas F Berbari

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 69 citations in OpenAlex.

  1. Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies.Journal of cell communication and signaling · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Primary cilia dysfunction: A critical driver of metabolic diseases (Review).International journal of molecular medicine · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. TheInternational journal of molecular sciences · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. GPR45 modulates GαScience (New York, N.Y.) · 2025
    Article
  17. Review
  18. Article
  19. Follistatin like-1 (Adipocyte · 2024
    Article
  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

4 authors at 2 institutions in 1 country.

Staci E EngleDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA.
Ruchi BansalDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA.
Patrick J AntonellisDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA.
Nicolas F BerbariDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA; Stark Neurosciences Research Institute, Indiana University, Indianapolis, IN, USA; Center for Diabetes and Metabolic Diseases, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: nberbari@iupui.edu.
Indiana University – Purdue University Indianapolis · USUniversity of Indianapolis · US

Funding

How Hedgehog Contributes to Centrally Mediated Energy Homeostasis?R01DK114008 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Nicolas F Berbari, Jeremy F Reiter · 2018 to 2026
$3.3M
NIDDK NIH HHS R01 DK114008
6 · The paper itself

Abstract

An emerging number of rare genetic disorders termed ciliopathies are associated with pediatric obesity. It is becoming clear that the mechanisms associated with cilia dysfunction and obesity in these syndromes are complex. In addition to ciliopathic syndromic forms of obesity, several cilia-associated signaling gene mutations also lead to morbid obesity. While cilia have critical and diverse functions in energy homeostasis including their roles in centrally mediated food intake as well as in peripheral tissues, many questions remain. Here, we briefly discuss the syndromic ciliopathies and monoallelic cilia signaling gene mutations associated with obesity. We also describe potential ways cilia may be involved in common obesity. We discuss how neuronal cilia impact food intake potentially through leptin signaling and changes in ciliary G protein-coupled receptor (GPCR) signaling. We highlight several recent studies that have implicated the potential for cilia in peripheral tissues such as adipose and the pancreas to contribute to metabolic dysfunction. Then we discuss the potential for cilia to impact energy homeostasis through their roles in both development and adult tissue homeostasis. The studies discussed in this review highlight how a comprehensive understanding of the requirement of cilia for the regulation of diverse biological functions will contribute to our understanding of common forms of obesity.

Indexed as

Adaptor Proteins, Signal TransducingAdipose TissueAdultAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsChildCiliaCiliopathiesEatingGene Expression RegulationHumansHypothalamusLeptinNeuronsObesity, MorbidPancreasAdaptor Proteins, Signal TransducingAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanLEP protein, humanLeptinRPGRIP1L protein, humanAdiposeAlström syndromeBardet-Biedl syndromeCiliaCiliopathyFTOGPCRG protein-coupled receptorsHedgehogHypothalamusIntraflagellar transportLeptinNeuronsObesityPancreasRpgrip1lTransition zone

Identifiers

PMID32466971
PMCPMC8739279
OpenAlexW3029458106

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.