Evidence map›Paper›PMID 27177220›Full record

ArticleOncotarget2016

Intralesional rose bengal in melanoma elicits tumor immunity via activation of dendritic cells by the release of high mobility group box 1.

Hao Liu, Pasquale Patrick Innamarato, Krithika Kodumudi, Amy Weber, Satoshi Nemoto, John L Robinson, Georgina Crago, Timothy McCardle, Erica Royster, Amod A Sarnaik and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 75 citations in OpenAlex.

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  16. Suppression of the malignancy of mammary tumor in mice model by inactivated preparation ofVeterinary research forum : an international quarterly journal · 2022
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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

11 authors at 1 institution in 1 country.

Hao LiuDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Pasquale Patrick InnamaratoDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Krithika KodumudiDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Amy WeberDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Satoshi NemotoDepartment of Translational Science, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
John L RobinsonFlow Cytometry Core Facility, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Georgina CragoDepartment of Cutaneous Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Timothy McCardleDepartment of Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Erica RoysterDepartment of Cutaneous Data Management, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Amod A SarnaikDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Shari Pilon-ThomasDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Moffitt Cancer Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Co-Stimulation to Enhance Adoptive Cell Therapy for Metastatic MelanomaK23CA178083 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI SARNAIK, AMOD · 2013 to 2017
$826k
NCI NIH HHS K23 CA178083NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

Intralesional (IL) therapy is under investigation to treat dermal and subcutaneous metastatic cancer. Rose bengal (RB) is a staining agent that was originally used by ophthalmologists and in liver function studies. IL injection of RB has been shown to induce regression of injected and uninjected tumors in murine models and clinical trials. In this study, we have shown a mechanism of tumor-specific immune response induced by IL RB. In melanoma-bearing mice, IL RB induced regression of injected tumor and inhibited the growth of bystander lesions mediated by CD8+ T cells. IL RB resulted in necrosis of tumor cells and the release of High Mobility Group Box 1 (HMGB1), with increased dendritic cell (DC) infiltration into draining lymph nodes and the activation of tumor-specific T cells. Treatment of DC with tumor supernatants increased the ability of DCs to stimulate T cell proliferation, and blockade of HMGB1 in the supernatants suppressed DC activity. Additionally, increased HMGB1 levels were measured in the sera of melanoma patients treated with IL RB. These results support the role of IL RB to activate dendritic cells at the site of tumor necrosis for the induction of a systemic anti-tumor immune response.

Indexed as

AdultAgedAnimalsAntineoplastic AgentsCD8-Positive T-LymphocytesCell Line, TumorCell ProliferationDendritic CellsFemaleHEK293 CellsHMGA1a ProteinHumansLeukocytes, MononuclearMaleMelanomaMelanoma, ExperimentalAntineoplastic AgentsHMGA1a ProteinRose Bengaldendritic cellshigh mobility group box 1intralesional therapymelanomarose bengal

Identifiers

PMID27177220
PMCPMC5122358
OpenAlexW2347143110

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.