Evidence map›Paper›PMID 40988573›Full record

ReviewHistology and histopathology2026

Crumbs3: Expression and biological significance in normal and neoplastic tissues.

Hidekazu Iioka, Akane Kitta-Kunihiro, Chiemi Ikude, Eisaku Kondo

Abstract readReview
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In one paragraph

Review in Histology and histopathology, 2026. 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

4 authors.

Hidekazu IiokaDivision of Tumor Biology, Faculty of Medical Technology, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, Japan. hiioka@nupals.ac.jp.
Akane Kitta-KunihiroDivision of Tumor Pathology, NIR-PIT Research Institute, Kansai Medical University, Osaka, Japan.
Chiemi IkudeDivision of Tumor Pathology, NIR-PIT Research Institute, Kansai Medical University, Osaka, Japan.
Eisaku KondoDivision of Tumor Pathology, NIR-PIT Research Institute, Kansai Medical University, Osaka, Japan. kondo.eis@kmu.ac.jp.

Funding

Japan Society for the Promotion of Science (JSPS) 17K08737Japan Society for the Promotion of Science (JSPS) 20K07368Japan Society for the Promotion of Science (JSPS) 26870692
6 · The paper itself

Abstract

Cellular polarity plays a fundamental role in tissue organization and homeostasis, and its disruption is closely linked to tumorigenesis. Crumbs3 (CRB3), a conserved polarity protein, is essential for epithelial morphogenesis, tight-junction formation, and barrier function. This review summarizes current knowledge regarding CRB3 expression in normal and malignant human tissues and its dual roles in cancer progression. Systematic immunohistochemical analyses revealed strong CRB3 expression in non-neoplastic glandular epithelia of the gastrointestinal, hepato-pancreato-biliary, renal, and respiratory tracts, as well as in fetal tissues, suggesting its importance in organ development and maintenance. In neoplastic tissues-represented by colorectal adenocarcinoma and oral squamous cell carcinoma-CRB3 expression is preserved or even enhanced compared with normal tissues, which promotes tumor cell migration, triggering invasion/metastasis as well as cellular proliferation through signaling pathways involving FGFR and RhoA activation. Conversely, previous studies reported that CRB3 functions as a tumor suppressor, based on findings that CRB3 expression induces loss of epithelial-mesenchymal transition, whereas loss of CRB3 expression attenuates the integrity of tight junctions, resulting in significantly poorer prognosis in certain cancers. Current data thus suggest that the biological role of CRB3 in tumors is complex. Whether CRB3 acts as a tumor accelerator or suppressor may depend on the individual-specific, unique characteristics of tumor cells. Understanding these dual functions may contribute to the development of novel polarity-targeted therapeutic strategies for cancers of differing origin.

Indexed as

Membrane ProteinsNeoplasmsAnimalsCell PolarityEpithelial-Mesenchymal TransitionHumansMembrane GlycoproteinsCRB3 protein, humanMembrane GlycoproteinsMembrane Proteins

Identifiers

PMID40988573

What Socratic holds

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Registered trials

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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 Socratic graph.