Evidence map›Paper›PMID 40952339›Full record

ArticleThe Journal of pathology2025

Chromosomal instability and genomic alterations in cholangiocarcinoma from Northeastern Thailand.

Raksawan Deenonpoe, Molly A Guscott, Sasithorn Watcharadetwittaya, Isabel L McNeill, Daniela Moralli, Nadeem Shaikh, Sarah E McClelland

Abstract read
In one paragraph

Article in The Journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Raksawan Deenonpoe *Barts Cancer Institute, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0002-8387-6061
Molly A Guscott *Barts Cancer Institute, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0003-1307-5450
Sasithorn WatcharadetwittayaDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0000-0001-7952-0583
Isabel L McNeillBarts Cancer Institute, Queen Mary University of London, London, UK.ORCID https://orcid.org/0009-0009-8778-965X
Daniela MoralliNuffield Department of Medicine, Oxford, UK.ORCID https://orcid.org/0000-0001-7977-8496
Nadeem ShaikhBarts Cancer Institute, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0003-1797-2271
Sarah E McClellandBarts Cancer Institute, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0002-9987-4511

Funding

Cancer Research UK C355/A25137Khon Kaen University, Thailand IN68046Mark FoundationMedical Research CouncilNational Science Research and Innovation FundNational Science Research and Innovation Fund (NSRF), ThailandUKRI
6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) is a lethal cancer of the bile duct and is a major health concern in several parts of the world, including northeastern Thailand, where CCA incidence is the highest due to the endemic liver fluke Opisthorchis viverrini. Multiple studies have characterised genomic alterations in CCA tumours, and specific chromosomal alterations can predict prognosis. However, it is not known whether chromosomal instability (CIN), ongoing genomic alteration characteristic of most cancer types, is present in CCA tumours. In this study we leveraged a panel of cancer cell lines derived from fluke-positive CCA patients, as well as a matched normal cholangiocyte line as a control, to characterise CIN in CCA. We observed elevated rates of chromosome segregation errors compared to normal cells, although overall CIN rates were lower than those for highly genomically unstable cancers, such as colorectal or ovarian cancer. Chromosome segregation errors in CCA cell lines were potentially driven by elevated DNA replication stress and centrosome duplication. Single-cell genome sequencing and karyotyping of the cell lines showed extensive structural and numerical chromosomal aberrations, as well as copy number alterations that were heterogeneous between individual cells, supporting the presence of ongoing CIN in these cell line models. Low-pass whole-genome sequencing of 33 CCA tumour samples with matched normal tissue from northeastern Thailand, a liver fluke-endemic region showed increased whole and subchromosomal level alterations, with a higher extent of genomic alterations in intrahepatic tumours compared to extrahepatic. Eight tumours carried focal amplifications and/or deletions involving known cancer genes, as well as potential chromosomal instability-associated genes, including CCNE1 amplifications and a rare amplification of BRCA1. This study provides increased understanding of the rate and potential mechanisms of CIN in CCA that may inform new therapeutic strategies that synergise with specific ongoing CIN mechanisms. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaChromosomal InstabilityAgedCell Line, TumorChromosome AberrationsDNA Copy Number VariationsFemaleHumansMaleMiddle AgedThailandcholangiocarcinomachromosomal instabilitycopy number alterationsheterogeneityliver flukeNorthern Thailand.single‐cell sequencing

Identifiers

PMID40952339
PMCPMC12531121

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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.