Evidence map›Paper›PMID 35775614›Full record

ArticleeLife2022

Response to immune checkpoint blockade improved in pre-clinical model of breast cancer after bariatric surgery.

Laura M Sipe, Mehdi Chaib, Emily B Korba, Heejoon Jo, Mary Camille Lovely, Brittany R Counts, Ubaid Tanveer, Jeremiah R Holt, Jared C Clements, Neena A John and 12 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Murine Models of Obesity-Related Cancer Risk.Cancer prevention research (Philadelphia, Pa.) · 2025
    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

22 authors at 3 institutions in 1 country.

Laura M SipeDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.ORCID 0000-0001-7848-3848
Mehdi ChaibDepartment of Pharmaceutical Sciences, College of Pharmacy, The University of Tennessee Health Science Center, Memphis, United States.
Emily B KorbaDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.ORCID 0000-0001-7422-9084
Heejoon JoDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Mary Camille LovelyDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Brittany R CountsIntegrative Muscle Biology Laboratory, Laboratory, Division of Rehabilitation Sciences, College of Health Professions, University of Tennessee Health Science Center, Memphis, United States.
Ubaid TanveerDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Jeremiah R HoltDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Jared C ClementsDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Neena A JohnDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Deidre DariaOffice of Vice Chancellor for Research, University of Tennessee Health Science Center, Memphis, United States.
Tony N MarionOffice of Vice Chancellor for Research, University of Tennessee Health Science Center, Memphis, United States.
Margaret S BohmDepartment of Microbiology, Immunology, and Biochemistry, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Radhika SekhriDepartment of Pathology, University of Tennessee Health Science Center, Memphis, United States.
Ajeeth K PingiliDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Bin TengDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
James A CarsonIntegrative Muscle Biology Laboratory, Laboratory, Division of Rehabilitation Sciences, College of Health Professions, University of Tennessee Health Science Center, Memphis, United States.
D Neil HayesDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Matthew J DavisDepartment of Surgery, Division of Bariatric Surgery, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.
Katherine L CookDepartment of Surgery, Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston Salem, United States.
Joseph F PierreDepartment of Microbiology, Immunology, and Biochemistry, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.ORCID 0000-0002-4248-1290
Liza MakowskiDepartment of Medicine, Division of Hematology and Oncology, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States.ORCID 0000-0002-5337-8037
University of Tennessee Health Science Center · USUniversity of Wisconsin–Madison · USWake Forest University · US

Funding

UNITS: The UNC / UT National Clinical Trials Network Group Integrated Translational Science Production and Consultation CenterUG1CA233333 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAYES, DAVID N, MERKER, JASON DEREK · 2019 to 2025
$4.8M
Role of microbial-modulated bile acid receptor signaling in breast cancerR01CA253329 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Katherine Loree Cook, Liza Makowski-Hayes · 2020 to 2026
$3.0M
Transdisciplinary Research in Energetics and Cancer (TREC) Training GrantR25CA203650 · NCI · YALE UNIVERSITY · PI IRWIN, MELINDA L · 2016 to 2025
$2.9M
Cachexia in ApcMin/+ mice: The role of IL-6R01CA121249 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CARSON, JAMES A · 2008 to 2018
$2.7M
Obesity-driven Metabolic and Molecular Biomarkers of Metformin Response in Endometrial CancerR37CA226969 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BAE-JUMP, VICTORIA LIN · 2018 to 2024
$2.5M
RNA sequencing analysis of CancerU24CA210988 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAYES, DAVID N, HOADLEY, KATHERINE A. · 2016 to 2020
$2.1M
Determining susceptibility loci in triple negative breast cancer using a novel pre-clinical modelR01CA262112 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Liza Makowski-Hayes · 2022 to 2026
$2.0M
Pan-cancer genomic characterization of human papillomavirus associated tumorsF30CA265224 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI HOLT, JEREMIAH R. · 2022 to 2025
$186k
The role of bile acids to ameliorate obesity driven triple negative breast cancerF32CA250192 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SIPE, LAURA MARIE · 2021 to 2022
$80k
NCI NIH HHS F30 CA265224NCI NIH HHS F32 CA250192NCI NIH HHS R01 CA121249NCI NIH HHS R01 CA253329NCI NIH HHS R01 CA262112NCI NIH HHS R25 CA203650NCI NIH HHS R37 CA226969NCI NIH HHS U24 CA210988NCI NIH HHS UG1 CA233333
6 · The paper itself

Abstract

Bariatric surgery is a sustainable weight loss approach, including vertical sleeve gastrectomy (VSG). Obesity exacerbates tumor growth, while diet-induced weight loss impairs progression. It remains unknown how bariatric surgery-induced weight loss impacts cancer progression or alters response to therapy. Using a pre-clinical model of obesity followed by VSG or diet-induced weight loss, breast cancer progression and immune checkpoint blockade therapy were investigated. Weight loss by VSG or weight-matched dietary intervention before tumor engraftment protected against obesity-exacerbated tumor progression. However, VSG was not as effective as diet in reducing tumor burden despite achieving similar weight and adiposity loss. Leptin did not associate with changes in tumor burden; however, circulating IL-6 was elevated in VSG mice. Uniquely, VSG tumors displayed elevated inflammation and immune checkpoint ligand PD-L1+ myeloid and non-immune cells. VSG tumors also had reduced T lymphocytes and markers of cytolysis, suggesting an ineffective anti-tumor microenvironment which prompted investigation of immune checkpoint blockade. While obese mice were resistant to immune checkpoint blockade, anti-PD-L1 potently impaired tumor progression after VSG through improved anti-tumor immunity. Thus, in formerly obese mice, surgical weight loss followed by immunotherapy reduced breast cancer burden. Finally, we compared transcriptomic changes in adipose tissue after bariatric surgery from patients and mouse models. A conserved

Indexed as

Bariatric SurgeryNeoplasmsAnimalsGastrectomyImmune Checkpoint InhibitorsMiceMice, ObeseObesityWeight LossImmune Checkpoint Inhibitorsbreast cancercancer biologyimmune checkpointimmunosuppressionimmunotherapymetabolic surgerymouseobesityPD-L1sleeve gastrectomy

Identifiers

PMID35775614
PMCPMC9342954
OpenAlexW4283745189

What OpenQuestion holds

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LicenceCC BY
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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.