Evidence map›Paper›PMID 31413529›Full record

ArticleWorld journal of gastroenterology2019

Honokiol-enhanced cytotoxic T lymphocyte activity against cholangiocarcinoma cells mediated by dendritic cells pulsed with damage-associated molecular patterns.

Arunya Jiraviriyakul, Worawat Songjang, Pongsathorn Kaewthet, Phachsita Tanawatkitichai, Punyapat Bayan, Sutatip Pongcharoen

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  8. Forkhead box M1 recruits FoxP3Immunity, inflammation and disease · 2022
    Article
  9. Review
  10. The role of tumor-infiltrating lymphocytes in cholangiocarcinoma.Journal of experimental & clinical cancer research : CR · 2022
    Review
  11. Review
  12. Review
  13. Article
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  16. Cholangiocarcinoma: novel therapeutic targets.Expert opinion on therapeutic targets · 2020
    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

6 authors at 1 institution in 1 country.

Arunya JiraviriyakulBiomedical Science Graduate School, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok 65000, Thailand.
Worawat SongjangBiomedical Science Graduate School, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok 65000, Thailand.
Pongsathorn KaewthetDepartment of Medical technology, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok 65000, Thailand.
Phachsita TanawatkitichaiDepartment of Medical technology, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok 65000, Thailand.
Punyapat BayanDepartment of Medical technology, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok 65000, Thailand.
Sutatip PongcharoenBiomedical Science Graduate School, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok 65000, Thailand. sutatipp@nu.ac.th.
Naresuan University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCholangiocarcinoma or biliary tract cancer has a high mortality rate resulting from late presentation and ineffective treatment strategy. Since immunotherapy by dendritic cells (DC) may be beneficial for cholangiocarcinoma treatment but their efficacy against cholangiocarcinoma was low. We suggest how such anti-tumor activity can be increased using cell lysates derived from an honokiol-treated cholangiocarcinoma cell line (KKU-213L5).

aimTo increase antitumour activity of DCs pulsed with cell lysates derived from honokiol-treated cholangiocarcinoma cell line (KKU-213L5).

methodsThe effect of honokiol, a phenolic compound isolated from

resultsHonokiol can effectively activate cholangiocarcinoma apoptosis and increase the release of damage-associated molecular patterns. DCs loaded with cell lysates derived from honokiol-treated tumour cells enhanced priming and stimulated T lymphocyte proliferation and type I cytokine production. T lymphocytes stimulated with DCs pulsed with cell lysates of honokiol-treated tumour cells significantly increased specific killing of human cholangiocarcinoma cells compared to those associated with DCs pulsed with cell lysates of untreated cholangiocarcinoma cells.

conclusionThe present findings suggested that honokiol was able to enhance the immunogenicity of cholangiocarcinoma cells associated with increased effectiveness of DC-based vaccine formulation. Treatment of tumour cells with honokiol offers a promising approach as an

Indexed as

Allyl CompoundsBile Duct NeoplasmsBiphenyl CompoundsCancer VaccinesCell Line, TumorCell ProliferationCholangiocarcinomaDendritic CellsHealthy VolunteersHumansImmunogenicity, VaccineImmunotherapyLignansLymphocyte ActivationPhenolsT-Lymphocytes, CytotoxicAllyl CompoundsBiphenyl CompoundsCancer VaccineshonokiolLignansPhenolsCholangiocarcinomaDamage-associated molecular patternsDendritic cellsHonokiolTumor cell lysates

Identifiers

PMID31413529
PMCPMC6689815
OpenAlexW2964654029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.