Evidence map›Paper›PMID 35646680›Full record

ArticleFrontiers in oncology2022

A Novel Karyoplasmic Ratio-Based Automatic Recognition Method for Identifying Glioma Circulating Tumor Cells.

Xinyi Zhu, Shen Wen, Shuhang Deng, Gao Wu, Ruyong Tian, Ping Hu, Liguo Ye, Qian Sun, Yang Xu, Gang Deng and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

14 authors at 4 institutions in 1 country.

Xinyi ZhuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Shen WenSchool of Physics and Technology, Wuhan University, Wuhan, China.
Shuhang DengDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Gao WuDepartment of Circulating Tumor Cells, YZY (Youzhiyou) Medical Technological Company, Wuhan, China.
Ruyong TianDepartment of Reagent Antibody, Genscript Biotech Corporation, Nanjing, China.
Ping HuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Liguo YeDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Qian SunDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Yang XuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Gang DengDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Dong ZhangSchool of Physics and Technology, Wuhan University, Wuhan, China.
Shuang YangSchool of Physics and Technology, Wuhan University, Wuhan, China.
Yangzhi QiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Qianxue ChenDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Wuhan University · CNRenmin Hospital of Wuhan University · CNGuilin University of Aerospace Technology · CNWuhan YZY Biopharma (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Detection of circulating tumor cells (CTCs) is a promising technology in tumor management; however, the slow development of CTC identification methods hinders their clinical utility. Moreover, CTC detection is currently challenging owing to major issues such as isolation and correct identification. To improve the identification efficiency of glioma CTCs, we developed a karyoplasmic ratio (KR)-based identification method and constructed an automatic recognition algorithm. We also intended to determine the correlation between high-KR CTC and patients' clinical characteristics. Methods: CTCs were isolated from the peripheral blood samples of 68 glioma patients and analyzed using DNA-seq and immunofluorescence staining. Subsequently, the clinical information of both glioma patients and matched individuals was collected for analyses. ROC curve was performed to evaluate the efficiency of the KR-based identification method. Finally, CTC images were captured and used for developing a CTC recognition algorithm. Results: KR was a better parameter than cell size for identifying glioma CTCs. We demonstrated that low CTC counts were independently associated with isocitrate dehydrogenase (IDH) mutations ( Conclusion: Our findings remarkably increased the efficiency of detecting glioma CTCs and revealed a correlation between CTC counts and patients' clinical characteristics. This will allow researchers to further investigate the clinical utility of CTCs. Moreover, our automatic recognition algorithm can maintain high precision in the CTC identification process, shorten the time and cost, and significantly reduce the burden on clinicians.

Indexed as

automatic recognition algorithmcirculating tumor cellsclinical imagegliomakaryoplasmic ratio

Identifiers

PMID35646680
PMCPMC9137408
OpenAlexW4280643169

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LicenceCC BY
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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.