Evidence map›Paper›PMID 40686460›Full record

ArticleScience progress

Higher expression of high-mobility group box 1 in cholangiocarcinoma and association with cell growth, in vitro migration and invasion, and chemo-drug sensitivity.

Arunya Jiraviriyakul, Samitanan Promchai, Chatchai Nensat, Suphakit Khutanthong, Nun Singpan, Worawat Songjang

Abstract read
In one paragraph

Article in Science progress. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Arunya JiraviriyakulIntegrative Biomedical Research Unit (IBRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, Thailand.
Samitanan PromchaiBiomedical Sciences Program, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, Thailand.
Chatchai NensatIntegrative Biomedical Research Unit (IBRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, Thailand.
Suphakit KhutanthongDepartment of Pathology, Faculty of Medicine, Naresuan University, Phitsanulok, Thailand.
Nun SingpanDepartment of Pathology, Faculty of Medicine, Naresuan University, Phitsanulok, Thailand.
Worawat SongjangIntegrative Biomedical Research Unit (IBRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, Thailand.ORCID 0000-0002-7799-2947

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveCholangiocarcinoma is a lethal malignancy with an increasing incidence and mortality worldwide. Numerous studies have indicated that high-mobility group box 1 is associated with cancer progression. The modulation of subcellular high-mobility group box 1 expression is a major cause of chemotherapeutic drug resistance. This study aimed to demonstrate the role of high-mobility group box 1 in cholangiocarcinoma, including proving the concept of high-mobility group box 1 expression in patients with cholangiocarcinoma, cancer cell growth, migration, invasion, and the modulation of chemotherapeutic drug sensitivity in cholangiocarcinoma cells.MethodsTwenty paraffin-embedded tissue samples were analyzed for high-mobility group box 1 expression using immunohistochemistry. High-mobility group box 1 expression was silenced in KKU-213AL5 cells through siRNA transfection, followed by in vitro assays to assess cell proliferation, migration, invasion, and drug sensitivity. Furthermore, the role of high-mobility group box 1 in regulating growth and metastasis-related signaling pathways was investigated using immunoblotting and protein-protein interaction analysis.ResultsThe results showed that high-mobility group box 1 was highly expressed in cholangiocarcinoma tissues compared to adjacent tissues (

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaHMGB1 ProteinAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationCisplatinDeoxycytidineDrug Resistance, NeoplasmFemaleGemcitabineGene Expression Regulation, NeoplasticHumansMaleNeoplasm InvasivenessAntineoplastic AgentsCisplatinDeoxycytidineGemcitabineHMGB1 ProteinHMGB1 protein, humanantimetastaticcholangiocarcinomacisplatingemcitabineHMGB1oxaliplatin

Identifiers

PMID40686460
PMCPMC12280535

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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.