Evidence map›Paper›PMID 40354349›Full record

ArticlePloS one2025

Distinct chromosome abnormality patterns for differential diagnosis of hepatocellular carcinoma and cholangiocarcinoma.

Wantakan Ngamsangiam, Sutheemon Techa-Ay, Prakasit Sa-Ngiamwibool, Sasithorn Watcharadetwittaya, Raksawan Deenonpoe, Anchalee Techasen, Natruja Sridakhun, Sureerat Padthaisong, Malinee Thanee

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

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5 · Who and what money

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9 authors.

Wantakan NgamsangiamDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Sutheemon Techa-AyDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Prakasit Sa-NgiamwiboolDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Sasithorn WatcharadetwittayaDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Raksawan DeenonpoeDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Anchalee TechasenCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0000-0002-4230-5641
Natruja SridakhunDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Sureerat PadthaisongFaculty of Allied Health Sciences, Burapha University, Chonburi, Thailand.
Malinee ThaneeDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0009-0007-6163-3740

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) are primary liver cancers with overlapping histopathological features, making accurate diagnosis challenging. This study aimed to identify chromosomal abnormalities that could aid in differentiating these cancers using chromosome microarray analysis (CMA). We analyzed ten frozen tumor tissues each of HCC and CCA, identifying distinct patterns of chromosomal gains and losses. HCC exhibited gains in regions 1p36.32, 1q23.3-q24.1, 3q21.3, 4p16.1, 5q31.1, and 11p15.5, and losses in 2p15, 3p11.1-q11.1, 4q12, 5p12-q11.1, 7q11.23, 14q23.2, 17p11.2, 17p13.3, 22q12.1, 22q12.2-q12.3, and 22q13.2. In contrast, CCA showed gains in 5p13.2, 5p14.1, 8p12-p11.23, 8p22, and 19p13.2, and losses in 1q31.1, 1q42.13, 3p25.3, 6p12.1, 6p25.3, and 17q21.33. Heatmap analysis revealed 17 distinct chromosomal regions between the two groups including 2q14.2, 4p16.3, 5q32, 7p14.3, 7p22.1, 7q11.21, 7q11.23, 7q21.3, 7q22.1, 10q21.3, 18q23, 19p13.2, 19q13.2, 21q21.3, 21q22.13, 22q11.21, and 22q12.2. Among these 1p36.32, 19p13.2, and 19q13.2 emerged as potential biomarkers for differential diagnosis. These findings may aid in confirming cases with overlapping histopathological features contribute to the development of diagnostic tools and improved targeted therapies for HCC and CCA.

Indexed as

Bile Duct NeoplasmsCarcinoma, HepatocellularCholangiocarcinomaChromosome AberrationsLiver NeoplasmsAdultAgedDiagnosis, DifferentialFemaleHumansMaleMiddle Aged

Identifiers

PMID40354349
PMCPMC12068623

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