Evidence map›Paper›PMID 37689690›Full record

ArticleNature communications2023

Chemical-induced phase transition and global conformational reorganization of chromatin.

Tengfei Wang, Shuxiang Shi, Yuanyuan Shi, Peipei Jiang, Ganlu Hu, Qinying Ye, Zhan Shi, Kexin Yu, Chenguang Wang, Guoping Fan and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  9. Modulation of AAV transduction and integration targeting by topoisomerase poisons.Molecular therapy. Methods & clinical development · 2024
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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

16 authors at 2 institutions in 1 country.

Tengfei Wang *School of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China.
Shuxiang Shi *School of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China.
Yuanyuan Shi *Shanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 200125, Shanghai, China.
Peipei Jiang *Shanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 200125, Shanghai, China.
Ganlu Hu *Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, 201210, Shanghai, China.
Qinying YeSchool of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China.ORCID http://orcid.org/0000-0002-3696-1810
Zhan ShiSchool of Physical Science and Technology, ShanghaiTech University, 201210, Shanghai, China.
Kexin YuSchool of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China.
Chenguang WangShanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 200125, Shanghai, China.
Guoping FanShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, 201210, Shanghai, China.ORCID http://orcid.org/0000-0001-5235-6410
Suwen ZhaoSchool of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China.ORCID http://orcid.org/0000-0001-5609-434X
Hanhui MaSchool of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China.ORCID http://orcid.org/0000-0002-4788-2106
Alex C Y ChangShanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 200125, Shanghai, China.ORCID http://orcid.org/0000-0001-9441-4033
Zhi LiSchool of Physical Science and Technology, ShanghaiTech University, 201210, Shanghai, China.ORCID http://orcid.org/0000-0003-2770-6364
Qian BianShanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 200125, Shanghai, China. qianbian@shsmu.edu.cn.ORCID http://orcid.org/0000-0001-7022-2213
Chao-Po LinSchool of Life Science and Technology, ShanghaiTech University, 201210, Shanghai, China. linzhb@shanghaitech.edu.cn.ORCID http://orcid.org/0000-0002-1457-1635
ShanghaiTech University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemicals or drugs can accumulate within biomolecular condensates formed through phase separation in cells. Here, we use super-resolution imaging to search for chemicals that induce phase transition within chromatin at the microscale. This microscopic screening approach reveals that adriamycin (doxorubicin) - a widely used anticancer drug that is known to interact with chromatin - specifically induces visible local condensation and global conformational change of chromatin in cancer and primary cells. Hi-C and ATAC-seq experiments systematically and quantitatively demonstrate that adriamycin-induced chromatin condensation is accompanied by weakened chromatin interaction within topologically associated domains, compartment A/B switching, lower chromatin accessibility, and corresponding transcriptomic changes. Mechanistically, adriamycin complexes with histone H1 and induces phase transition of H1, forming fibrous aggregates in vitro. These results reveal a phase separation-driven mechanism for a chemotherapeutic drug.

Indexed as

Biomolecular CondensatesChromatinChromatin Immunoprecipitation SequencingDoxorubicinGene Expression ProfilingChromatinDoxorubicin

Identifiers

PMID37689690
PMCPMC10492836
OpenAlexW4386579549

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.