Evidence map›Paper›PMID 37758874›Full record

ArticleCommunications biology2023

PC3T: a signature-driven predictor of chemical compounds for cellular transition.

Lu Han, Bin Song, Peilin Zhang, Zhi Zhong, Yongxiang Zhang, Xiaochen Bo, Hongyang Wang, Yong Zhang, Xiuliang Cui, Wenxia Zhou

Abstract read
In one paragraph

Article in Communications biology, 2023. 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

10 authors.

Lu Han *Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
Bin Song *Department of Pancreatic Surgery, Changhai Hospital, Second Military Medical University, 200438, Shanghai, China.
Peilin Zhang *National Center for Liver Cancer, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, 200438, Shanghai, China.
Zhi ZhongFudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, 200032, Shanghai, China.
Yongxiang ZhangBeijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
Xiaochen BoDepartment of Bioinformatics, Institute of Health Service and Transfusion Medicine, 100850, Beijing, China.ORCID http://orcid.org/0000-0003-1911-7922
Hongyang WangNational Center for Liver Cancer, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, 200438, Shanghai, China.ORCID http://orcid.org/0000-0002-4709-3334
Yong ZhangInstitute for Regenerative Medicine, Shanghai East Hospital, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China. yzhang@tongji.edu.cn.ORCID http://orcid.org/0000-0001-6316-2734
Xiuliang CuiNational Center for Liver Cancer, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, 200438, Shanghai, China. wafyai@163.com.ORCID http://orcid.org/0000-0002-0165-5020
Wenxia ZhouBeijing Institute of Pharmacology and Toxicology, 100850, Beijing, China. zhouwx@bmi.ac.cn.ORCID http://orcid.org/0000-0002-6175-4821

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular transitions hold great promise in translational medicine research. However, therapeutic applications are limited by the low efficiency and safety concerns of using transcription factors. Small molecules provide a temporal and highly tunable approach to overcome these issues. Here, we present PC3T, a computational framework to enrich molecules that induce desired cellular transitions, and PC3T was able to consistently enrich small molecules that had been experimentally validated in both bulk and single-cell datasets. We then predicted small molecule reprogramming of fibroblasts into hepatic progenitor-like cells (HPLCs). The converted cells exhibited epithelial cell-like morphology and HPLC-like gene expression pattern. Hepatic functions were also observed, such as glycogen storage and lipid accumulation. Finally, we collected and manually curated a cell state transition resource containing 224 time-course gene expression datasets and 153 cell types. Our framework, together with the data resource, is freely available at http://pc3t.idrug.net.cn/ . We believe that PC3T is a powerful tool to promote chemical-induced cell state transitions.

Indexed as

Cellular ReprogrammingFibroblastsEpithelial CellsStem CellsTranscription FactorsTranscription Factors

Identifiers

PMID37758874
PMCPMC10533498

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.