Evidence map›Paper›PMID 42279400›Full record

ReviewCancers2026

Clinical Implications of Polyploid Giant Cancer Cells in Solid Tumors: Biology, Diagnosis, and Therapeutic Considerations.

Hiroshi Imaoka, Masafumi Ikeda, Masashi Wakabayashi, Kumiko Umemoto, Tomoyuki Satake, Yu Sunakawa, Hideki Ueno, Kazuo Hara, Fumio Nagashima, Shigeki Kataoka and 18 more

Abstract readReview
In one paragraph

Review in Cancers, 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

28 authors.

Hiroshi ImaokaDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0003-0584-0095
Masafumi IkedaDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0002-4050-2086
Masashi WakabayashiClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Kumiko UmemotoDepartment of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki 216-8511, Japan.
Tomoyuki SatakeDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Yu SunakawaDepartment of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki 216-8511, Japan.ORCID 0000-0002-0163-7543
Hideki UenoDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan.
Kazuo HaraDepartment of Gastroenterology, Aichi Cancer Center Hospital, Nagoya 464-8681, Japan.ORCID 0000-0002-4699-6136
Fumio NagashimaDepartment of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo 181-8611, Japan.
Shigeki KataokaDepartment of Medical Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
Terumasa HisanoDepartment of Hepato-Biliary-Pancreatology, National Hospital Organization Kyushu Cancer Center, Fukuoka 811-1347, Japan.
Yuko SuzukiDepartment of Gastroenterology, Saitama Cancer Center, Saitama 362-0806, Japan.
Akinori AsagiDepartment of Gastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama 791-0245, Japan.
Kazuhiko ShiojiDepartment of Internal Medicine, Niigata Cancer Center Hospital, Niigata 951-8566, Japan.ORCID 0000-0002-9916-208X
Kotoe OshimaDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan.
Kunihiro TsujiDepartment of Gastroenterology, Ishikawa Prefectural Central Hospital, Kanazawa 920-8530, Japan.
Kazuyoshi OhkawaDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka 541-8567, Japan.
Ikuya MikiDepartment of Gastroenterological Oncology, Hyogo Cancer Center, Akashi 673-8558, Japan.
Yasuyuki KawamotoDivision of Cancer Center, Hokkaido University Hospital, Sapporo 060-8648, Japan.ORCID 0000-0002-7706-0015
Taro YamashitaDepartment of Gastroenterology, Kanazawa University Hospital, Kanazawa 920-8641, Japan.
Makoto UenoDepartment of Gastroenterology, Kanagawa Cancer Center, Yokohama 241-8515, Japan.
Yujiro KawakamiDepartment of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine, Sapporo 060-8556, Japan.
Hiroaki NaganoDepartment of Gastroenterological, Breast and Endocrine Surgery, Yamaguchi University Graduate School of Medicine, Ube 755-8505, Japan.
Hiroyuki OkuyamaDepartment of Medical Oncology, Kagawa University Hospital, Miki 761-0793, Japan.
Atsushi NaganumaDepartment of Gastroenterology, National Hospital Organization Takasaki General Medical Center, Takasaki 370-0829, Japan.ORCID 0000-0003-0663-0102
Rei SuzukiDepartment of Gastroenterology, School of Medicine, Fukushima Medical University, Fukushima 960-1295, Japan.ORCID 0000-0002-4049-0484
Junji FuruseDepartment of Gastroenterology, Kanagawa Cancer Center, Yokohama 241-8515, Japan.ORCID 0000-0003-0663-6117
Japan Oncology Network in Hepatobiliary and Pancreas

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyploid giant cancer cells (PGCCs) are characterized by abnormal enlargement and considerable polyploidy. Though the presence of giant cancer cells has been documented for decades, they remain not fully understood, especially in clinical practice, due to diagnostic challenges, and confusion regarding synonyms for PGCCs still exists. Thus, understanding PGCCs may be a key clue to overcoming them. This review offers a comprehensive overview of PGCCs, integrating insights from basic research and clinical studies to enhance understanding of their complex biology and clinical implications. In basic research, PGCCs are known to emerge under various stressors, including chemotherapy exposure, radiation, viral infection, and hypoxic environments. These cells play crucial roles in tumor progression through multiple mechanisms: enhancing genetic diversity, and facilitating metastatic spread via asymmetrical cell division and genomic instability. In clinical studies, PGCC-containing tumors have been shown to exhibit marked treatment resistance and are associated with a poor prognosis across multiple solid tumor types, including prostate, lung, and pancreatic cancers. Despite these therapeutic challenges, taxane-based chemotherapy has shown promising results in PGCC-containing tumors, such as pleomorphic carcinoma and undifferentiated carcinoma. Furthermore, emerging targeted therapies directed at specific pathways in PGCCs, particularly those involving TP53, represent potential strategies to improve clinical outcomes of patients with PGCC-containing tumors.

Indexed as

cancer-associated macrophage-like celldormancymultinucleated giant cancer cellosteoclast-like giant cellpleomorphic cancer cellpolyaneuploid cancer cellpolyploid giant cancer cellpolyploidizationundifferentiated carcinoma

Identifiers

PMID42279400
PMCPMC13257396

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.