Evidence map›Paper›PMID 30150136›Full record

ReviewTrends in endocrinology and metabolism: TEM2018

Salt-Inducible Kinases: Physiology, Regulation by cAMP, and Therapeutic Potential.

Marc N Wein, Marc Foretz, David E Fisher, Ramnik J Xavier, Henry M Kronenberg

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

92 citing papers in PubMed, 139 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Upregulation of Parathyroid Hormone Receptor 1 (International journal of molecular sciences · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Control of alveolar bone development, homeostasis, and socket healing by salt-inducible kinases.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article

32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Marc N WeinEndocrine Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: mnwein@partners.org.
Marc ForetzINSERM, U1016, Institut Cochin, Paris 75014, France; CNRS, UMR8104, Paris 75014, France; Université Paris Descartes, Sorbonne Paris Cité, Paris 75014, France.
David E FisherCutaneous Biology Research Center, Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Ramnik J XavierGastrointestinal Unit and Center for the Study of Inflammatory Bowel Disease, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Center for Microbiome Informatics and Therapeutics, MIT, Cambridge, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Henry M KronenbergEndocrine Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Harvard University · USDélégation Paris 5 · FRMassachusetts General Hospital · US

Funding

Tissue Phenotyping CoreP01DK011794 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MANNSTADT, MICHAEL · 1986 to 2023
$44.4M
Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
Genetic and Pathway Analysis CoreU19AI109725 · NIAID · WASHINGTON UNIVERSITY · PI ALLEN, PAUL M · 2014 to 2018
$32.7M
Autoimmunity Center of Excellence Clinical Research ProgramUM1AI110498 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WOFSY, DAVID · 2014 to 2019
$31.4M
Transcriptional mechanisms and melanomaP01CA163222 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Kai W Wucherpfennig · 2013 to 2026
$25.3M
The MITF transcriptional network: melanoma risk and carcinogenesisR01AR043369 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 1996 to 2026
$9.4M
Therapeutic strategies for treatment of giant congenital melanocytic neviR01AR072304 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 2017 to 2026
$3.9M
Skeletal Phenotyping CoreP30AR066261 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI KRONENBERG, HENRY M. · 2014 to 2018
$3.5M
A druggable dependency in low-MITF/high-AXL melanoma: preclinical efficacy and mechanism of action in a key treatment-resistant subclass.R01CA222871 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FISHER, DAVID E · 2018 to 2022
$1.8M
Dissecting the roles of class IIa HDACs in osteocyte biologyK08AR067285 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI WEIN, MARC NATHAN · 2015 to 2019
$698k
Skeletal effects of the small molecule SIK inhibitor YKL-05-099R03AR072150 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI WEIN, MARC NATHAN · 2017 to 2018
$171k
Reducing cartilage destruction in osteoarthritis with the small molecule SIK inhibitor YKL-05-099R03AR072903 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI WEIN, MARC NATHAN · 2018 to 2019
$167k
NCI NIH HHS P01 CA163222NCI NIH HHS R01 CA222871NIAID NIH HHS U19 AI109725NIAID NIH HHS UM1 AI110498NIAMS NIH HHS K08 AR067285NIAMS NIH HHS P30 AR066261NIAMS NIH HHS R01 AR043369NIAMS NIH HHS R01 AR072304NIAMS NIH HHS R03 AR072150NIAMS NIH HHS R03 AR072903NIDDK NIH HHS P01 DK011794NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

Salt-inducible kinases (SIKs) represent a subfamily of AMP-activated protein kinase (AMPK) family kinases. Initially named because SIK1 (the founding member of this kinase family) expression is regulated by dietary salt intake in the adrenal gland, it is now apparent that a major biological role of these kinases is to control gene expression in response to extracellular cues that increase intracellular levels of cAMP. Here, we review four physiologically relevant examples of how cAMP signaling impinges upon SIK cellular function. By focusing on examples of cAMP-mediated SIK regulation in gut myeloid cells, bone, liver, and skin, we highlight recent advances in G protein-coupled receptor (GPCR) signal transduction. New knowledge regarding the role of SIKs in GPCR signaling has led to therapeutic applications of novel small molecule SIK inhibitors.

Indexed as

AMP-Activated Protein KinasesHumansProtein Kinase InhibitorsProtein KinasesProtein Serine-Threonine KinasesReceptors, G-Protein-CoupledSignal TransductionAMP-Activated Protein KinasesProtein Kinase InhibitorsProtein KinasesProtein Serine-Threonine KinasesReceptors, G-Protein-Coupledsalt-inducible kinase-2, humanSIK1 protein, humanSIK3 protein, humanglucose metabolisminflammationkinaseosteoporosissecond messengersskin pigmentation

Identifiers

PMID30150136
PMCPMC6151151
OpenAlexW2888508916

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.