Evidence map›Paper›PMID 36658417›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2023

Circulating tumour cell isolation, analysis and clinical application.

XiaoLi Zhang, PeiPei Xie, KaiTai Zhang, Wen Zhang

Abstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Liquid Biopsy in the Clinical Management of Cancers.International journal of molecular sciences · 2024
    Review
  11. Article
  12. 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

4 authors.

XiaoLi Zhang *State Key Laboratory of Molecular Oncology, Department of Etiology and Carcinogenesis, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
PeiPei Xie *State Key Laboratory of Molecular Oncology, Department of Etiology and Carcinogenesis, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
KaiTai ZhangState Key Laboratory of Molecular Oncology, Department of Etiology and Carcinogenesis, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China. zhangkt@cicams.ac.cn.
Wen ZhangDepartment of Immunology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China. zhangwen@cicams.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCirculating tumour cells (CTCs) are cancer cells that circulate in the bloodstream after being shed from solid tumours. They can lead to tumour recurrence and metastasis. CTCs play a significant role as biomarkers for early diagnosis, therapy response monitoring, and prognostication. However, CTCs are rare and heterogeneous, with usually only a single-digit number in one millilitre of blood. Additionally, a circadian rhythm is involved in the release of CTCs into the peripheral circulation. Due to these biological properties, higher demands are placed on the isolation of CTCs, and current capture methods struggle to enrich all CTCs present in blood. As yet, these limitations have hampered the clinical application of CTCs.

conclusionsIn this review, we focus on the biological properties and clinical applications of CTCs and current CTC enrichment and isolation methods. Combined enrichment methods based on physical and biological properties are considered instrumental for the development of highly specific and sensitive CTC capture methods. The utilization of CTCs in conjunction with other liquid biopsy components (such as ctDNA) may yield more clinically useful information and the circadian rhythmicity of CTC release may change the way to evaluate and treat patients.

Indexed as

Neoplastic Cells, CirculatingCell SeparationHumansLiquid BiopsyBiological propertiesCirculating tumour cellsClinical applicationsIsolation

Identifiers

PMID36658417
PMCPMC12974714

What OpenQuestion holds

Textmetadata
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.