Evidence map›Paper›PMID 35540548›Full record

ArticleRSC advances2018

LC-MS based cell metabolic profiling of tumor cells: a new predictive method for research on the mechanism of action of anticancer candidates.

Hua Wang, Jia-Hui Hu, Cui-Chai Liu, Min Liu, Zheng Liu, Li-Xin Sun

Abstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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

6 authors.

Hua WangDepartment of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University Shenyang 110016 China sunlixin67@yahoo.com +86 02443520600.
Jia-Hui HuDepartment of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University Shenyang 110016 China sunlixin67@yahoo.com +86 02443520600.ORCID https://orcid.org/0000-0001-8488-8278
Cui-Chai LiuDepartment of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University Shenyang 110016 China sunlixin67@yahoo.com +86 02443520600.
Min LiuDepartment of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University Shenyang 110016 China sunlixin67@yahoo.com +86 02443520600.
Zheng LiuGLP Center, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University Shenyang China.
Li-Xin SunDepartment of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University Shenyang 110016 China sunlixin67@yahoo.com +86 02443520600.ORCID https://orcid.org/0000-0001-6197-259X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the process of anticancer drug development, research on the mechanism of action remains a major obstacle. In the present study, a cell metabolic profiling based discriminatory model was designed to give general direction on anticancer candidate mechanisms. Firstly, ultra-performance liquid chromatography in tandem with high-definition mass spectrometry was applied to obtain a comprehensive metabolic view of 12 human tumor cells. Secondly, multivariate data analysis was used to assess the metabolites' variations, and 42 metabolites were identified as the main contributors to the discrimination of different groups. Then a metabolite-based prediction model was constructed for the first time and verified by cross validation (

Identifiers

PMID35540548
PMCPMC9080298

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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.