Evidence map›Paper›PMID 34889941›Full record

ArticleThe Journal of cell biology2022

Chromosome compartmentalization alterations in prostate cancer cell lines model disease progression.

Rebeca San Martin, Priyojit Das, Renata Dos Reis Marques, Yang Xu, Justin M Roberts, Jacob T Sanders, Rosela Golloshi, Rachel Patton McCord

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  6. Design Space and Declarative Grammar for 3D Genomic Data Visualization.IEEE transactions on visualization and computer graphics · 2026
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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

8 authors at 2 institutions in 1 country.

Rebeca San MartinDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, TN.ORCID 0000-0001-7249-3922
Priyojit DasUniversity of Tennessee - Oak Ridge National Lab (UT-ORNL) Graduate School of Genome Science and Technology, University of Tennessee, Knoxville, TN.
Renata Dos Reis MarquesDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, TN.ORCID 0000-0001-6274-8303
Yang XuUniversity of Tennessee - Oak Ridge National Lab (UT-ORNL) Graduate School of Genome Science and Technology, University of Tennessee, Knoxville, TN.ORCID 0000-0003-4173-4337
Justin M RobertsDepartment of Genitourinary Medical Oncology and the David H. Koch Center for Applied Research of Genitourinary Cancer, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-6304-1713
Jacob T SandersDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, TN.ORCID 0000-0002-4065-8742
Rosela GolloshiDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, TN.
Rachel Patton McCordDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, TN.ORCID 0000-0003-0010-5323
University of Tennessee at Knoxville · USThe University of Texas MD Anderson Cancer Center · US

Funding

Folding, Misfolding, and Unfolding: How human 3D genome structure resists, adapts, or succumbs to physical stresses in health and diseaseR35GM133557 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI Rachel Patton McCord · 2019 to 2026
$2.7M
NIGMS NIH HHS R35 GM133557NIGMS NIH HHS R35GM133557
6 · The paper itself

Abstract

Prostate cancer aggressiveness and metastatic potential are influenced by gene expression and genomic aberrations, features that can be influenced by the 3D structure of chromosomes inside the nucleus. Using chromosome conformation capture (Hi-C), we conducted a systematic genome architecture comparison on a cohort of cell lines that model prostate cancer progression, from normal epithelium to bone metastasis. We describe spatial compartment identity (A-open versus B-closed) changes with progression in these cell lines and their relation to gene expression changes in both cell lines and patient samples. In particular, 48 gene clusters switch from the B to the A compartment, including androgen receptor, WNT5A, and CDK14. These switches are accompanied by changes in the structure, size, and boundaries of topologically associating domains (TADs). Further, compartment changes in chromosome 21 are exacerbated with progression and may explain, in part, the genesis of the TMPRSS2-ERG translocation. These results suggest that discrete 3D genome structure changes play a deleterious role in prostate cancer progression. .

Indexed as

Disease ProgressionModels, BiologicalCell Line, TumorChromatinChromosomes, HumanCohort StudiesGenes, NeoplasmGenome, HumanHumansMaleNeoplasm MetastasisProstatic NeoplasmsSerine EndopeptidasesTranscriptional ActivationChromatinSerine EndopeptidasesTMPRSS2 protein, human

Identifiers

PMID34889941
PMCPMC8669499
OpenAlexW4200537317

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.