Evidence map›Paper›PMID 28151483›Full record

ArticleCell death & disease2017

Colon cancer cell treatment with rose bengal generates a protective immune response via immunogenic cell death.

Jianzhong Qin, Nicholas Kunda, Guilin Qiao, Jed F Calata, Krunal Pardiwala, Bellur S Prabhakar, Ajay V Maker

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

45 citing papers in PubMed, 78 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Rose Bengal-Chitosan Nanocomposites for Oral Administration.Nanomaterials (Basel, Switzerland) · 2025
    Article
  10. Article
  11. Article
  12. High Efficacy of Rose Bengal in Reducing the Pathogenicity ofInternational journal of microbiology · 2025
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

7 authors at 2 institutions in 1 country.

Jianzhong QinDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL, USA.
Nicholas KundaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL, USA.
Guilin QiaoDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL, USA.
Jed F CalataDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL, USA.
Krunal PardiwalaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL, USA.
Bellur S PrabhakarDepartment of Microbiology and Immunology, University of Illinois at Chicago, Chicago, IL, USA.
Ajay V MakerDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL, USA.
Advocate Illinois Masonic Medical Center · USUniversity of Illinois Chicago · US

Funding

Enhancing anti-tumor immune responses in colon cancer metastasesK08CA190855 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MAKER, AJAY V. · 2014 to 2018
$909k
NCI NIH HHS K08 CA190855
6 · The paper itself

Abstract

Immunotherapeutic approaches to manage patients with advanced gastrointestinal malignancies are desired; however, mechanisms to incite tumor-specific immune responses remain to be elucidated. Rose bengal (RB) is toxic at low concentrations to malignant cells and may induce damage-associated molecular patterns; therefore, we investigated its potential as an immunomodulator in colon cancer. Murine and human colon cancer lines were treated with RB (10% in saline/PV-10) for cell cycle, cell death, and apoptosis assays. Damage-associated molecular patterns were assessed with western blot, ELISA, and flow cytometry. In an immunocompetent murine model of colon cancer, we demonstrate that tumors regress upon RB treatment, and that RB induces cell death in colon cancer cells through G2/M growth arrest and predominantly necrosis. RB-treated colon cancer cells expressed distinct hallmarks of immunogenic cell death (ICD), including enhanced expression of calreticulin and heat-shock protein 90 on the cell surface, a decrease in intracellular ATP, and the release of HMGB1. To confirm the ICD phenotype, we vaccinated immunocompetent animals with syngeneic colon cancer cells treated with RB. RB-treated tumors served as a vaccine against subsequent challenge with the same CT26 colon cancer tumor cells, and vaccination with in vitro RB-treated cells resulted in slower tumor growth following inoculation with colon cancer cells, but not with syngeneic non-CT26 cancer cells, suggesting a specific antitumor immune response. In conclusion, RB serves as an inducer of ICD that contributes to enhanced specific antitumor immunity in colorectal cancer.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCalreticulinCell DeathCell Line, TumorColonic NeoplasmsHCT116 CellsHMGB1 ProteinHSP90 Heat-Shock ProteinsHT29 CellsHumansMiceMice, Inbred BALB CNecrosisRose BengalAntineoplastic AgentsCalreticulinHMGB1 ProteinHSP90 Heat-Shock ProteinsRose Bengal

Identifiers

PMID28151483
PMCPMC5386459
OpenAlexW2585458561

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.