Evidence map›Paper›PMID 34582557›Full record

ArticleBlood2022

PEG10 amplification at 7q21.3 potentiates large-cell transformation in cutaneous T-cell lymphoma.

Fengjie Liu, Yumei Gao, Bufang Xu, Shan Xiong, Shengguo Yi, Jingru Sun, Zhuojing Chen, Xiangjun Liu, Yingyi Li, Yuchieh Lin and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Blood, 2022. 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
6.6field-weighted citation impact, top 3% 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, 40 citations in OpenAlex.

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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

19 authors at 2 institutions in 2 countries.

Fengjie LiuDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Yumei GaoDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Bufang XuDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Shan XiongDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Shengguo YiDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Jingru SunDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Zhuojing ChenDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Xiangjun LiuDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Yingyi LiDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0003-1097-0230
Yuchieh LinDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Yujie WenDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0003-4004-4158
Yao QinDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Shuxia YangDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Hang LiDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Trilokraj TejasviDepartment of Dermatology, University of Michigan, Ann Arbor, MI; and.
Lam TsoiDepartment of Dermatology, University of Michigan, Ann Arbor, MI; and.ORCID 0000-0003-1627-5722
Ping TuDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Xianwen RenBiomedical Pioneering Innovation Center (BIOPIC), Peking University, Beijing 100034, China.ORCID 0000-0002-8558-5401
Yang WangDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China.
Peking University · CNUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycosis fungoides (MF), the most common form of cutaneous T-cell lymphoma, undergo large-cell transformation (LCT) in the late stage, manifesting aggressive behavior, resistance to treatments, and poor prognosis, but the mechanisms involved remain unclear. To identify the molecular driver of LCT, we collected tumor samples from 133 MF patients and performed whole-transcriptome sequencing on 49 advanced-stage MF patients, followed by integrated copy number inference and genomic hybridization. Tumors with LCT showed unique transcriptional programs and enriched expressions of genes at chr7q. Paternally expressed gene 10 (PEG10), an imprinted gene at 7q21.3, was ectopically expressed in malignant T cells from LCT, driven by 7q21.3 amplification. Mechanistically, aberrant PEG10 expression increased cell size, promoted cell proliferation, and conferred treatment resistance by a PEG10/KLF2/NF-κB axis in in vitro and in vivo models. Pharmacologically targeting PEG10 reversed the phenotypes of proliferation and treatment resistance in LCT. Our findings reveal new molecular mechanisms underlying LCT and suggest that PEG10 inhibition may serve as a promising therapeutic approach in late-stage aggressive T-cell lymphoma.

Indexed as

AnimalsApoptosis Regulatory ProteinsCell Line, TumorCell Transformation, NeoplasticDNA-Binding ProteinsFemaleGene AmplificationGene Expression Regulation, NeoplasticGenomic ImprintingHumansLymphoma, T-Cell, CutaneousMiceMice, Inbred NODMice, SCIDMycosis FungoidesRNA-Binding ProteinsApoptosis Regulatory ProteinsDNA-Binding ProteinsPEG10 protein, humanPeg10 protein, mouseRNA-Binding Proteins

Identifiers

PMID34582557
PMCPMC8893588
OpenAlexW3203820526

What OpenQuestion holds

Textmetadata
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.