Evidence map›Paper›PMID 31843981›Full record

ArticleCancer research2020

Integrin β4-Targeted Cancer Immunotherapies Inhibit Tumor Growth and Decrease Metastasis.

Shasha Ruan, Ming Lin, Yong Zhu, Lawrence Lum, Archana Thakur, Runming Jin, Wenlong Shao, Yalei Zhang, Yangyang Hu, Shiang Huang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.2field-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

57 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Article
  3. Halofuginone is a Molecular Glue Degrader of Integrin β4.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. PD-L1 on Tumor-Derived Extracellular Vesicles Induces CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Breaking Immunosuppression to Enhance Cancer Stem Cell-Targeted Immunotherapy.International journal of biological sciences · 2025
    Review
  20. 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

14 authors at 8 institutions in 2 countries.

Shasha RuanRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Ming LinRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Yong ZhuGuangzhou Improve Medical Instruments Co., Ltd. Guangzhou, Guangdong, China.
Lawrence LumDivision of Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, Virginia.
Archana ThakurDivision of Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, Virginia.
Runming JinUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Wenlong ShaoThe First Affiliated Hospital of Guangzhou Medical University, Guangzhou Institute of Respiratory Health, Guangzhou, China.
Yalei ZhangThe First Affiliated Hospital of Guangzhou Medical University, Guangzhou Institute of Respiratory Health, Guangzhou, China.
Yangyang HuDepartment of Rheumatology and Immunology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Shiang HuangUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Elaine M HurtMedimmune LLC, Gaithersburg, Maryland.
Alfred E ChangRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Max S WichaRogel Cancer Center, University of Michigan, Ann Arbor, Michigan. mwicha@umich.edu qiaoli@umich.edu.
Qiao LiRogel Cancer Center, University of Michigan, Ann Arbor, Michigan. mwicha@umich.edu qiaoli@umich.edu.
Michigan Center for Translational Pathology · USFirst Affiliated Hospital of Guangzhou Medical University · CNHuazhong University of Science and Technology · CNUniversity of Virginia · USAltimmune (United States) · USGuangzhou Medical University · CNTongji Hospital · CNWuhan University · CN

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Targeting breast cancer stem cellsR35CA197585 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WICHA, MAX S. · 2016 to 2022
$6.4M
Breast Cancer Treatment with Antibody Targeted T CellsR01CA092344 · NCI · WAYNE STATE UNIVERSITY · PI LUM, LAWRENCE G · 2002 to 2012
$4.6M
Targeting Neuroblastoma with armed T cellsR01CA182526 · NCI · WAYNE STATE UNIVERSITY · PI CHEUNG, NAI-KONG V, LUM, LAWRENCE G · 2014 to 2019
$3.9M
Enhancing neoadjuvant chemotherpay responses with targeted T cellsR01CA140314 · NCI · WAYNE STATE UNIVERSITY · PI BEPLER, GEROLD · 2010 to 2015
$2.5M
Characterization of Human Oral Cancer Initiating Cell (CIC) AntigensR56DE024385 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, QIAO · 2014 to 2014
$287k
NCATS NIH HHS UL1 TR000433NCI NIH HHS P30 CA044579NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA092344NCI NIH HHS R01 CA140314NCI NIH HHS R01 CA182526NCI NIH HHS R35 CA197585NIDCR NIH HHS R56 DE024385
6 · The paper itself

Abstract

Integrin β4 (ITGB4) has been shown to play an important role in the regulation of cancer stem cells (CSC). Immune targeting of ITGB4 represents a novel approach to target this cell population, with potential clinical benefit. We developed two immunologic strategies to target ITGB4: ITGB4 protein-pulsed dendritic cells (ITGB4-DC) for vaccination and adoptive transfer of anti-CD3/anti-ITGB4 bispecific antibody (ITGB4 BiAb)-armed tumor-draining lymph node T cells. Two immunocompetent mouse models were utilized to assess the efficacy of these immunotherapies in targeting both CSCs and bulk tumor populations: 4T1 mammary tumors and SCC7 head and neck squamous carcinoma cell line. Immunologic targeting of ITGB4 utilizing either ITGB4-DC or ITGB4 BiAb-T cells significantly inhibited local tumor growth and metastases in both the 4T1 and SCC7 tumor models. Furthermore, the efficacy of both of these ITGB4-targeted immunotherapies was significantly enhanced by the addition of anti-PD-L1. Both ITGB4-targeted immunotherapies induced endogenous T-cell cytotoxicity directed at CSCs as well as non-CSCs, which expressed ITGB4, and immune plasma-mediated killing of CSCs. As a result, ITGB4-targeted immunotherapy reduced not only the number of ITGB4

Indexed as

AnimalsAntibodies, BispecificB7-H1 AntigenCancer VaccinesCarcinogenesisCD3 ComplexCell Line, TumorDendritic CellsDisease Models, AnimalFemaleGene Knockout TechniquesHumansImmunotherapy, AdoptiveIntegrin beta4Lymph NodesMiceAntibodies, BispecificB7-H1 AntigenCancer VaccinesCd274 protein, mouseCD3 ComplexIntegrin beta4Itgb4 protein, mouse

Identifiers

PMID31843981
PMCPMC7024642
OpenAlexW2995510656

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.