Evidence map›Paper›PMID 40883446›Full record

ArticleScientific reports2025

Choline transporter-like protein 1 in tongue squamous cell carcinoma: implications for cell proliferation and differentiation.

Nao Hashimoto, Kei Nakajima, Yoshihiko Akashi, Katsutoshi Kokubun, Keisuke Sugahara, Akira Katakura, Kenichi Matsuzaka

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Nao HashimotoDepartment of Oral Pathobiological Science and Surgery, Tokyo Dental College, Tokyo, Japan. hashimotonao@tdc.ac.jp.
Kei NakajimaDepartment of Pathology, Tokyo Dental College, Tokyo, Japan. nakajimakei@tdc.ac.jp.ORCID http://orcid.org/0000-0003-4092-3208
Yoshihiko AkashiDepartment of Pathology, Tokyo Dental College, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2262-5610
Katsutoshi KokubunDepartment of Pathology, Tokyo Dental College, Tokyo, Japan.ORCID http://orcid.org/0000-0002-0613-6481
Keisuke SugaharaDepartment of Oral Pathobiological Science and Surgery, Tokyo Dental College, Tokyo, Japan.ORCID http://orcid.org/0000-0002-0260-396X
Akira KatakuraDepartment of Oral Pathobiological Science and Surgery, Tokyo Dental College, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9761-1267
Kenichi MatsuzakaDepartment of Pathology, Tokyo Dental College, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have indicated moderate to high choline transporter-like protein 1 (CTL1) expression in colon, pancreatic, breast, lung, and glioma cancers. However, studies on CTL1 in oral squamous cell carcinoma (OSCC), a highly invasive cancer, remain limited. We aimed to investigate the expression and localization of CTL1 in OSCC and its association with cell proliferation. Using in vitro experiments, we evaluated CTL1 expression and localization in the OSCC cell lines HSC-3 and HSC-4 by immunocytochemistry and western blotting. A cell proliferation assay was performed using hemicolinium-3, a choline uptake inhibitor. Using in vivo and ex vivo experiments, we assessed CTL1 expression in rat and human tongue cancer tissues by immunohistochemical and immunofluorescent staining. Here, we show that CTL1 is strongly expressed intracellularly and localized in organelles of HSC-3 and HSC-4 cells. CTL1 significantly accumulated around the nucleus in Ki67-positive cells with proliferative potential, suggesting increased production and transport of CTL1. Conversely, the number of cells in the HC-3 treated group in both HSC-3 and HSC-4 cells decreased. These results suggest that intracellular production of CTL1 is further increased in Ki67-positive cells, and choline uptake may lead to cell proliferation. In vivo and ex vivo experiments revealed high CTL1 expression in tongue cancer, with stronger expression in well-differentiated tumors than that in poorly-differentiated ones. Our study demonstrates that CTL1 is associated with OSCC proliferation and tumor differentiation. These findings suggest that CTL1 may function as a potential marker for tumor differentiation and progression of OSCC.

Indexed as

Carcinoma, Squamous CellCell DifferentiationOrganic Cation Transport ProteinsTongue NeoplasmsAnimalsAntigens, CDCell Line, TumorCell ProliferationCholineGene Expression Regulation, NeoplasticHemicholinium 3HumansMaleRatsAntigens, CDCholineHemicholinium 3Organic Cation Transport ProteinsSLC44A1 protein, human

Identifiers

PMID40883446
PMCPMC12397295

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