Evidence map›Paper›PMID 41929383›Full record

ArticleJournal of the Endocrine Society2026

Insulin receptor expression and its association with hyperinsulinemia in triple negative breast cancer.

Alexis J Engel, Krupa Samuel, Ilana R Bass, Sylvia Lin, Irini Markella Antoniou, Radhi Yagnik, Elisa Port, Sheldon M Feldman, Neil B Friedman, Susan K Boolbol and 9 more

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

19 authors.

Alexis J EngelDepartment of Medical Education, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID https://orcid.org/0000-0003-1708-0986
Krupa SamuelDepartment of Surgery, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Ilana R BassDivision of Endocrinology, Diabetes and Bone Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sylvia LinDepartment of Population Health Science and Policy, Center for Health Equity and Community Engaged Research, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Irini Markella AntoniouDivision of Endocrinology, Diabetes and Bone Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Radhi YagnikDepartment of Population Health Science and Policy, Center for Health Equity and Community Engaged Research, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Elisa PortDepartment of Surgery, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sheldon M FeldmanDepartment of Surgery, Montefiore Medical Center, Albert Einstein College of Medicine, New York, NY 10461, USA.
Neil B FriedmanDepartment of Surgery, Mercy Medical Center, Baltimore, MD 21202, USA.
Susan K BoolbolNuvance Health, Poughkeepsie, NY 12601, USA.
Brigid KilleleaDepartment of Surgery, Brigham and Women's Hospital, Boston, MA 02115, USA.
Melissa PilewskieDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Lydia ChoiDepartment of Surgery, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Christopher A GalifiDepartment of Pharmacology, Physiology and Neuroscience, Center for Cell Signaling and Cancer Institute of New Jersey, Rutgers Biomedical and Health Sciences, Newark, NJ 07039, USA.
Teresa L WoodDepartment of Pharmacology, Physiology and Neuroscience, Center for Cell Signaling and Cancer Institute of New Jersey, Rutgers Biomedical and Health Sciences, Newark, NJ 07039, USA.
Nathan G KaseDepartment of Obstetrics, Gynecology, and Reproductive Science, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Derek LeRoithDivision of Endocrinology, Diabetes and Bone Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Nina A BickellDepartment of Population Health Science and Policy, Center for Health Equity and Community Engaged Research, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Emily J GallagherDivision of Endocrinology, Diabetes and Bone Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID https://orcid.org/0000-0002-7920-8474

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Mechanisms for the pro-metastatic effects of hyperinsulinemia on breast cancerR01CA128799 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LEROITH, DEREK · 2008 to 2018
$3.7M
Insulin Resistance and Breast Cancer Prognosis in Black & White WomenR01CA171558 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BICKELL, NINA A., LEROITH, DEREK · 2012 to 2017
$3.1M
Understanding how elevated triglycerides contribute to triple negative breast cancer growth and metastasisR37CA266853 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Emily Jane Gallagher · 2022 to 2026
$2.5M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA128799NCI NIH HHS R01 CA171558NCI NIH HHS R37 CA266853
6 · The paper itself

Abstract

Purpose: Hyperinsulinemia and tumor insulin receptor (IR) expression have been associated with triple negative breast cancer (TNBC) progression in preclinical models. We aimed to evaluate the expression of the IR, IGF-1 receptor (IGF-1R), and associated signaling protein expression in TNBC and their correlations with demographic and metabolic parameters in a population of women with TNBC. Methods: We identified cases of TNBC from our multi-institutional, cross-sectional study of self-identified Black and White women with newly diagnosed breast cancer. Survey, anthropometric, screening behavior, laboratory, and tumor pathology reports were collected, along with formalin-fixed paraffin embedded tumor samples. We performed immunohistochemistry (IHC) analysis and quantified the expression of IR, IGF-1R, phosphorylated Erk1/2 (pErk1/2), and FOXO3a. Clinical information was correlated with IHC scoring. Results: There were 93 TNBC cases. IHC staining and quantification found that 63% of TNBC cases stained positive for IR, 73% for IGF-1R, 67% for FOXO3a, and 43% for pErk1/2. Positive IR staining was more prevalent in Black women than White women ( Conclusion: Tumor IR expression was associated with higher fasting insulin, and higher fasting insulin was more prevalent among Black women. Further studies are needed to determine the importance of hyperinsulinemia and tumor IR expression in the development of TNBC.

Indexed as

hyperinsulinemiainsulin receptortriple negative breast cancer

Identifiers

PMID41929383
PMCPMC13043147

What OpenQuestion holds

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Registered trials

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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.