Evidence map›Paper›PMID 38036052›Full record

ArticleExperimental cell research2024

Insulin promotes growth in breast cancer cells through the type I IGF receptor in insulin receptor deficient cells.

Marvis Monteiro, Xihong Zhang, Douglas Yee

Open access · hybridAbstract read
In one paragraph

Article in Experimental cell research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Breast Cancer and Metabolic Dysfunction-Associated Steatotic Liver Disease.International journal of molecular sciences · 2026
    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 3 institutions in 1 country.

Marvis MonteiroMasonic Cancer Center, University of Minnesota, Minneapolis, MN, 55455, USA; Purdue University, Heine Pharmacy Building, 575 Stadium Mall Drive, West Lafayette, IN, 47907-2091, USA.
Xihong ZhangMasonic Cancer Center, University of Minnesota, Minneapolis, MN, 55455, USA.
Douglas YeeMasonic Cancer Center, University of Minnesota, Minneapolis, MN, 55455, USA. Electronic address: yeexx006@umn.edu.
Purdue University West Lafayette · USUniversity of Minnesota, Duluth · USUniversity of Minnesota Medical Center · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller · 1998 to 2026
$100.4M
Disrupting insulin receptor function in breast cancerR01CA251600 · NCI · UNIVERSITY OF MINNESOTA · PI YEE, DOUGLAS · 2020 to 2024
$1.7M
NCI NIH HHS P30 CA077598NCI NIH HHS R01 CA251600
6 · The paper itself

Abstract

Breast cancer is the most common cancer in women. The upregulation of insulin-like growth factor (IGF) system observed in certain types of breast cancers was linked to growth, metastasis, and survival resulting in multiple strategies designed to target the type I IGF receptor (IGF-1R) in breast cancer. These attempts failed to prove beneficial and it has been suggested that insulin receptor (IR) could also play an important role in breast cancer biology. To better understand the IR's role in breast cancer cells, the receptor was deleted from MCF-7L cells using CRISPR technology, and fluorescence-assisted cell sorting was used to obtain clone 35 (CL35). It was found that CL35 activated signaling pathways upon insulin stimulation despite the absence of IR expression. We hypothesized that CL35 used a surrogate receptor for sustained growth and development. IGF-1R was able to activate insulin signaling and growth in CL35. Thus, insulin may play a central role in regulating breast cancer growth due to its ability to activate all the receptors of the IGF family. These findings argue that dual targeting of IR and IGF-IR may be required to inhibit breast cancer growth.

Indexed as

Breast NeoplasmsReceptor, InsulinCell Line, TumorFemaleHumansInsulinInsulin-Like Growth Factor IReceptor, IGF Type 1Receptors, SomatomedinIGF1R protein, humanInsulinInsulin-Like Growth Factor IReceptor, IGF Type 1Receptor, InsulinReceptors, SomatomedinBreast cancerCell-signalingCRISPRIGF systemInsulin receptorType I IGF receptor

Identifiers

PMID38036052
PMCPMC10842809
OpenAlexW4389081177

What OpenQuestion holds

Textmetadata
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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.