Evidence mapPaperPMID 35657145Full record

ArticleJournal of clinical laboratory analysis2022

Optimal whole blood dilution protocol for preprocessing samples prior to circulating tumor cell capture by size-based isolation.

Tianhao Fu, Sheng Li, Liang Wei, Shaoyi Huang, Yan Xue, Kai Cui

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. 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. 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

6 authors.

Tianhao FuDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID https://orcid.org/0000-0001-5191-2841
Sheng LiDepartment of Hepatobiliary Surgery, Shandong Cancer Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Liang WeiWuhan YZY Medical Science & Technology Co., Ltd, Wuhan, China.
Shaoyi HuangWuhan YZY Medical Science & Technology Co., Ltd, Wuhan, China.
Yan XueJinan Children's Hospital, Jinan, China.
Kai CuiDepartment of Hepatobiliary Surgery, Shandong Cancer Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.

Funding

2019 Jinan "University 20" Project 2019GXRC020Shandong First Medical University Academic Upgrading Scheme 2019QL004Start-up fund of Shandong Cancer Hospital 2020-PYB19Tarzan Scholar Special Project
6 · The paper itself

Abstract

backgroundThis study compared whole blood dilution versus density gradient centrifugation for pre-processing blood samples prior to circulating tumor cell (CTC) capture on the efficiency of CTC separation by size-based isolation. MATERIALS AND

methodsWhole blood from a healthy volunteer spiked with SKBR3 cells was used to optimize the whole blood dilution protocol for sample volume, dilution ratio, and paraformaldehyde (PFA) concentration. Whole blood from healthy volunteers spiked with SKBR3, A549, or PC3 cells, and whole blood from patients with advanced gastric, esophageal, or liver cancer, was used to compare pre-processing by the optimal whole blood dilution protocol with density-gradient centrifugation. All statistical evaluations were performed using Student t test of the Statistical Package for Social Sciences (SPSS version 17.0).

resultsIn blood samples from healthy volunteers, spiked SKBR3 cell recovery rates were highest in 5 ml of whole blood, diluted with 2.5 ml buffer, and fixed with 0.2% PFA, and spiked SKBR3, A549, and PC3 cell recovery rates from 5 ml whole blood were significantly greater when using the optimized whole blood dilution protocol (87.67% ± 1.76%, 79.50% ± 0.50% and 71.83% ± 1.04%, respectively) compared to density-gradient centrifugation (46.83 ± 1.76%, 37.00 ± 1.50% and 41.00 ± 1.50%, respectively).

Indexed as

Neoplastic Cells, CirculatingCell Line, TumorCell SeparationHumansblood dilutioncirculating tumor cellcirculating tumor microembolisize-based isolation

Identifiers

PMID35657145
PMCPMC9279958

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.