Evidence map›Paper›PMID 27520877›Full record

ArticleJournal of hepatology2017

Successful chemoimmunotherapy against hepatocellular cancer in a novel murine model.

Guangfu Li, Dai Liu, Timothy K Cooper, Eric T Kimchi, Xiaoqiang Qi, Diego M Avella, Ningfei Li, Qing X Yang, Mark Kester, C Bart Rountree and 5 more

Abstract read
In one paragraph

Article in Journal of hepatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. ModulatingJournal for immunotherapy of cancer · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Nanoliposome C6-Ceramide in combination with anti-CTLA4 antibody improves anti-tumor immunity in hepatocellular cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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

15 authors at 4 institutions in 1 country.

Guangfu Li *Department of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Dai Liu *Department of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Timothy K CooperComparative Medicine, Pennsylvania State University College of Medicine, Hershey, PA 17033.
Eric T KimchiDepartment of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Xiaoqiang QiDepartment of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Diego M AvellaRadiology and Neurosurgery, Pennsylvania State University College of Medicine, Hershey, PA 17033.
Ningfei LiDepartment of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Qing X YangRadiology and Neurosurgery, Pennsylvania State University College of Medicine, Hershey, PA 17033.
Mark KesterDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908.
C Bart RountreeBon Secours Children's Services, Richmond, VA 23226.
Jussuf T KaifiDepartment of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
David J ColeDepartment of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Don C RockeyDepartment of Medicine, Medical University of South Carolina, Charleston, SC 29425.
Todd D SchellDepartment of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey, PA 17033.
Kevin F Staveley-O'CarrollDepartment of Surgery, Division of Surgical Oncology, Medical University of South Carolina, Charleston, SC 29425.
Medical University of South Carolina · USMUSC Hollings Cancer Center · USPennsylvania State University · USUniversity of Virginia · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
CD8+ T Cell-Mediated Immunotherapy of Autochthonous SV40 T Antigen-Induced TumorsR01CA025000 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SCHELL, TODD D · 1985 to 2014
$5.0M
NO AND THE CELLULAR PATHOGENESIS OF PORTAL HYPERTENSIONR01DK057830 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ROCKEY, DON C. · 2000 to 2012
$2.6M
An Orthotopic Murine Model of HCC: Immunotolerance and PreventionR01CA164335 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI STAVELEY-O'CARROLL, KEVIN FINNBAR · 2012 to 2016
$1.5M
NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA025000NCI NIH HHS R01 CA164335NIDDK NIH HHS R01 DK057830
6 · The paper itself

Abstract

BACKGROUND &

aimsWe have established a clinically relevant animal model of hepatocellular cancer (HCC) in immune competent mice to elucidate the complex dialog between host immunity and tumors during HCC initiation and progression. Mechanistic findings have been leveraged to develop a clinically feasible anti-tumor chemoimmunotherapeutic strategy.

methodsIntraperitoneal injection of carbon tetrachloride and intrasplenic inoculation of oncogenic hepatocytes were combined to induce progressive HCCs in fibrotic livers of immunocompetent mice. Immunization and adoptive cell transfer (ACT) were used to dissect the tumor antigen-specific immune response. The ability of the tyrosine kinase inhibitor sunitinib to enhance immunotherapy in the setting of HCC was evaluated.

resultsThis new mouse model mimics human HCC and reflects its typical features. Tumor-antigen-specific CD8

conclusionTreg accumulation and upregulation of PD-1 provide two independent mechanisms to induce profound immune tolerance in HCC. Chemoimmunotherapy using Food and Drug Administration-approved sunitinib with anti-PD-1 antibodies achieved significant tumor control, supporting translation of this approach for the treatment of HCC patients. LAY SUMMARY: In the current study, we have established a clinically relevant mouse model which mimics human liver cancer. Using this unique model, we studied the response of the immune system to this aggressive cancer. Findings from this trial have led to the development of an innovative and clinically feasible chemoimmunotherapeutic strategy.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAdoptive TransferAnimalsCD8-Positive T-LymphocytesCytotoxicity, ImmunologicDisease Models, AnimalEnzyme InhibitorsHistocompatibility Antigens Class IIImmune ToleranceImmunotherapyIndolesMiceNeoplasm StagingProgrammed Cell Death 1 ReceptorPyrrolesEnzyme InhibitorsHistocompatibility Antigens Class IIIndolesProgrammed Cell Death 1 ReceptorPyrrolesSunitinibCancerChemoimmunotherapyCirculating tumor cell (CTC)Hepatocellular cancer (HCC)Immune checkpointProgrammed cell death protein 1 (PD-1)Regulatory T cells (Tregs)Sunitinib

Identifiers

PMID27520877
PMCPMC5167655
OpenAlexW2494328932

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.