Evidence map›Paper›PMID 36556357›Full record

ReviewLife (Basel, Switzerland)2022

The Insulin-like Growth Factor Signaling Pathway in Breast Cancer: An Elusive Therapeutic Target.

Ji-Sun Lee, Claire E Tocheny, Leslie M Shaw

Open access · goldAbstract readReview
In one paragraph

Review in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
7.1field-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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Bladder cancer risk factors: a comprehensive umbrella review of meta-analyses.International journal of surgery (London, England) · 2026
    Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Therapeutic delivery of albumin-binding siRNA targeting IRS2 to diverse cell types reduces mammary tumor growth.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. In silico approach andContemporary oncology (Poznan, Poland) · 2026
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
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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 1 institution in 1 country.

Ji-Sun LeeDepartment of Molecular, Cell & Cancer Biology, University of Massachusetts Chan Medical School, 364 Plantation St., Worcester, MA 01605, USA.
Claire E TochenyDepartment of Molecular, Cell & Cancer Biology, University of Massachusetts Chan Medical School, 364 Plantation St., Worcester, MA 01605, USA.ORCID 0000-0002-5791-7560
Leslie M ShawDepartment of Molecular, Cell & Cancer Biology, University of Massachusetts Chan Medical School, 364 Plantation St., Worcester, MA 01605, USA.
University of Massachusetts Chan Medical School · US

Funding

Adaptor protein function in breast cancerR01CA229910 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SHAW, LESLIE M · 2019 to 2023
$1.9M
IRS function in breast cancer progressionR01CA227993 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SHAW, LESLIE M · 2019 to 2023
$1.9M
NCI NIH HHS R01 CA227993NCI NIH HHS R01 CA229910NIH HHS CA227993NIH HHS CA229910
6 · The paper itself

Abstract

In this review, we provide an overview of the role of the insulin-like growth factor (IGF) signaling pathway in breast cancer and discuss its potential as a therapeutic target. The IGF pathway ligands, IGF-1 and IGF-2, and their receptors, primarily IGF-1R, are important for normal mammary gland biology, and dysregulation of their expression and function drives breast cancer risk and progression through activation of downstream signaling effectors, often in a subtype-dependent manner. The IGF signaling pathway has also been implicated in resistance to current therapeutic strategies, including ER and HER2 targeting drugs. Unfortunately, efforts to target IGF signaling for the treatment of breast cancer have been unsuccessful, due to a number of factors, most significantly the adverse effects of disrupting IGF signaling on normal glucose metabolism. We highlight here the recent discoveries that provide enthusiasm for continuing efforts to target IGF signaling for the treatment of breast cancer patients.

Indexed as

breast cancerIGF-1 receptor (IGF-1R)insulin-like growth factor (IGF)insulin receptor substrate (IRS) proteinssignal transductiontherapy

Identifiers

PMID36556357
PMCPMC9782138
OpenAlexW4310191279

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.