Evidence map›Paper›PMID 41381844›Full record

ArticleBritish journal of cancer2026

Urothelium marker UPK2 identifies aggressive colorectal cancers with distinct molecular and histological features.

Ville K Äijälä, Jouni Härkönen, Päivi Sirniö, Tuomo Mantere, Hanna Elomaa, Onni Sirkiä, Akseli Kehusmaa, Henna Karjalainen, Meeri Kastinen, Vilja V Tapiainen and 13 more

Abstract read
In one paragraph

Article in British journal of cancer, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

23 authors.

Ville K ÄijäläTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Jouni HärkönenDepartment of Pathology, Hospital Nova of Central Finland, Well Being Services County of Central Finland, Jyväskylä, Finland.
Päivi SirniöTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Tuomo MantereLaboratory of Cancer Genetics and Tumor Biology, Translational Medicine Research Unit, Medical Research Center Oulu and Biocenter Oulu, University of Oulu, Oulu, Finland.ORCID http://orcid.org/0000-0003-3284-4403
Hanna ElomaaResearch Program in Systems Oncology, University of Helsinki, Helsinki, Finland.
Onni SirkiäDepartment of Environmental and Biological Sciences, University of Eastern Finland, Kuopio, Finland.
Akseli KehusmaaTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Henna KarjalainenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Meeri KastinenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Vilja V TapiainenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Maarit AhtiainenCentral Finland Biobank, Hospital Nova of Central Finland, Well Being Services County of Central Finland, Jyväskylä, Finland.
Olli HelminenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Erkki-Ville WirtaDepartment of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, Tampere, Finland.
Jukka RintalaTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Sanna MeriläinenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Juha SaarnioTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Tero RautioTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.
Toni T SeppäläDepartment of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, Tampere, Finland.
Jan BöhmDepartment of Pathology, Hospital Nova of Central Finland, Well Being Services County of Central Finland, Jyväskylä, Finland.
Jukka-Pekka MecklinDepartment of Education and Research, Well Being Services County of Central Finland, Jyväskylä, Finland.
Anne TuomistoTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.ORCID http://orcid.org/0000-0002-9949-1887
Markus J MäkinenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.ORCID http://orcid.org/0000-0002-9200-4118
Juha P VäyrynenTranslational Medicine Research Unit, University of Oulu, and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland. juha.vayrynen@oulu.fi.ORCID http://orcid.org/0000-0002-8683-2996

Funding

Academy of Finland (Suomen Akatemia) 338657Jane ja Aatos Erkon Säätiö (Jane and Aatos Erkko Foundation) 21002Sigrid Juséliuksen Säätiö (Sigrid Jusélius Foundation) 240194Sigrid Juséliuksen Säätiö (Sigrid Jusélius Foundation) 240241Sigrid Juséliuksen Säätiö (Sigrid Jusélius Foundation) 250264Suomen Lääketieteen Säätiö (Finnish Medical Foundation) 6021Syöpäsäätiö (Cancer Foundation Finland) 59-5619Syöpäsäätiö (Cancer Foundation Finland) 69-7354
6 · The paper itself

Abstract

backgroundUroplakin-2 (UPK2) is a relatively specific marker for urothelial cancer, often used in the differential diagnosis of tumors of unknown origin. UPK2 expression has been observed in colorectal cancers (CRCs), prompting further investigation.

methodsUPK2 expression was analyzed in two independent CRC cohorts (N = 1851) and The Cancer Genome Atlas (N = 467). We investigated the histopathological, immunological, molecular, and clinical characteristics of UPK2-positive CRCs.

resultsUPK2 was expressed in 12% of CRCs and associated with adverse features including advanced stage, lymphovascular invasion, tumor budding, and micropapillary growth (p < 0.01). UPK2 positivity correlated with higher CRC-specific mortality in both cohorts (Cohort 1: HR 1.97, 95% CI 1.00-3.88; Cohort 2: HR 3.33, 95% CI 2.15-5.16). In the larger cohort, this association remained independent of other prognostic parameters (HR 2.31, 95% CI 1.46-3.65). UPK2-positive tumors showed reduced infiltration of CD3 + T cells, B cells, plasma cells, and M2-like macrophages. Molecularly, these tumors were associated with TP53 mutation, CMS4 subtype, and upregulation of genes linked to keratinization and squamous differentiation, such as KRT17 and DSG3 (p < 0.01).

conclusionsUPK2 marks a distinct subset of CRCs with poor prognosis, epithelial-mesenchymal transition, micropapillary growth, and squamous differentiation. These findings may affect the development of targeted therapies in precision medicine.

Indexed as

Biomarkers, TumorColorectal NeoplasmsUroplakin IIUrotheliumAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisBiomarkers, TumorUroplakin II

Identifiers

PMID41381844
PMCPMC12858874

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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.