Evidence map›Paper›PMID 40529216›Full record

ArticleEngineering in life sciences2025

Rapid Recovery and Short-Term Culture of Gastric Circulating Tumor Cells Using Microcavity Array.

Tomoko Yoshino, Tomohiro Takabayashi, Qian Bao, Tsuyoshi Tanaka, Ryo Negishi, Tatsu Shimoyama, Takeshi Sawada, Yusuke Kanemasa, Fumiaki Koizumi

Abstract read
In one paragraph

Article in Engineering in life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
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

9 authors.

Tomoko YoshinoDivision of Biotechnology and Life Science Institute of Engineering Tokyo University of Agriculture and Technology Koganei Tokyo Japan.ORCID https://orcid.org/0000-0002-4505-2774
Tomohiro TakabayashiDivision of Biotechnology and Life Science Institute of Engineering Tokyo University of Agriculture and Technology Koganei Tokyo Japan.
Qian BaoDivision of Biotechnology and Life Science Institute of Engineering Tokyo University of Agriculture and Technology Koganei Tokyo Japan.
Tsuyoshi TanakaDivision of Biotechnology and Life Science Institute of Engineering Tokyo University of Agriculture and Technology Koganei Tokyo Japan.
Ryo NegishiDivision of Biotechnology and Life Science Institute of Engineering Tokyo University of Agriculture and Technology Koganei Tokyo Japan.
Tatsu ShimoyamaDepartment of Medical Oncology Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan.
Takeshi SawadaDepartment of Medical Oncology Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan.
Yusuke KanemasaDepartment of Medical Oncology Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan.
Fumiaki KoizumiDepartment of Laboratory Medicine Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor cells (CTCs) hold significant promise for cancer diagnosis, prognosis, and treatment monitoring. We previously developed a technique for a single-cell filtering device known as the microcavity array (MCA), specifically designed for the efficient recovery of CTCs from whole blood samples. Efficient enrichment and release of cells from the MCA remains challenging because of cell adhesion that occurs on the MCA surface during the enrichment phase. This study investigated the effects of surface modification with 2-methacryloyloxyethyl phosphorylcholine (MPC) on the recovery efficiency of cancer cell lines from MCA. Scanning electron microscope (SEM) demonstrated reduced cell-substrate interactions, leading to improved recovery efficiency. Comparative analyses showed that the MCA method provided superior recovery efficiency and reduced processing time compared to traditional methods such as density gradient centrifugation (DGC), while maintaining cell viability and proliferative capacity. CTCs were successfully detected in patients with gastric cancer, and short-term cultures were achieved even when fewer than 20 CTCs per milliliter of blood were isolated. These findings emphasize the importance of surface modification for enhancing CTC isolation and the need for optimized culture conditions. The optimized MCA method offers a promising approach for rapid CTC recovery and potential integration with automated systems.

Indexed as

circulating tumor cellsCTC recoverygastric cancermicrocavity arrayshort‐term culture

Identifiers

PMID40529216
PMCPMC12167759

What OpenQuestion 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 OpenQuestion graph.