Evidence map›Paper›PMID 34382383›Full record

ArticleHaematologica2022

Whole-genome profiling of primary cutaneous anaplastic large cell lymphoma.

Armando N Bastidas Torres, Rutger C Melchers, Liana Van Grieken, Jacoba J Out-Luiting, Hailiang Mei, Cedrick Agaser, Thomas B Kuipers, Koen D Quint, Rein Willemze, Maarten H Vermeer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 17 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

11 authors at 1 institution in 1 country.

Armando N Bastidas TorresDepartment of Dermatology, Leiden University Medical Center, Leiden.
Rutger C MelchersDepartment of Dermatology, Leiden University Medical Center, Leiden.
Liana Van GriekenDepartment of Dermatology, Leiden University Medical Center, Leiden.
Jacoba J Out-LuitingDepartment of Dermatology, Leiden University Medical Center, Leiden.
Hailiang MeiSequencing Analysis Support Core, Leiden University Medical Center, Leiden.
Cedrick AgaserSequencing Analysis Support Core, Leiden University Medical Center, Leiden.
Thomas B KuipersSequencing Analysis Support Core, Leiden University Medical Center, Leiden.
Koen D QuintDepartment of Dermatology, Leiden University Medical Center, Leiden.
Rein WillemzeDepartment of Dermatology, Leiden University Medical Center, Leiden.
Maarten H VermeerDepartment of Dermatology, Leiden University Medical Center, Leiden.
Cornelis P TensenDepartment of Dermatology, Leiden University Medical Center, Leiden. c.p.tensen@lumc.nl.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cutaneous anaplastic large cell lymphoma (pcALCL), a hematological neoplasm caused by skin-homing CD30+ malignant T cells, is part of the spectrum of primary cutaneous CD30+ lymphoproliferative disorders. To date, only a small number of molecular alterations have been described in pcALCL and, so far, no clear unifying theme that could explain the pathogenetic origin of the disease has emerged among patients. In order to clarify the pathogenetic basis of pcALCL, we performed high-resolution genetic profiling (genome/transcriptome) of this lymphoma (n=12) by using whole-genome sequencing, whole-exome sequencing and RNA sequencing. Our study, which uncovered novel genomic rearrangements, copy number alterations and small-scale mutations underlying this malignancy, revealed that the cell cycle, T-cell physiology regulation, transcription and signaling via the PI-3-K, MAPK and G-protein pathways are cellular processes commonly impacted by molecular alterations in patients with pcALCL. Recurrent events affecting cancer-associated genes included deletion of PRDM1 and TNFRSF14, gain of EZH2 and TNFRSF8, small-scale mutations in LRP1B, PDPK1 and PIK3R1 and rearrangements involving GPS2, LINC-PINT and TNK1. Consistent with the genomic data, transcriptome analysis uncovered upregulation of signal transduction routes associated with the PI-3-K, MAPK and G-protein pathways (e.g., ERK, phospholipase C, AKT). Our molecular findings suggest that inhibition of proliferation-promoting pathways altered in pcALCL (particularly PI-3-K/AKT signaling) should be explored as potential alternative therapy for patients with this lymphoma, especially, for cases that do not respond to first-line skin-directed therapies or with extracutaneous disease.

Indexed as

Lymphoma, Large-Cell, AnaplasticLymphoma, Primary Cutaneous Anaplastic Large CellLymphoproliferative DisordersSkin Neoplasms3-Phosphoinositide-Dependent Protein KinasesFetal ProteinsHumansKi-1 AntigenProtein-Tyrosine KinasesProto-Oncogene Proteins c-akt3-Phosphoinositide-Dependent Protein KinasesFetal ProteinsKi-1 AntigenPDPK1 protein, humanProtein-Tyrosine KinasesProto-Oncogene Proteins c-aktTNK1 protein, human

Identifiers

PMID34382383
PMCPMC9244823
OpenAlexW3193128875

What OpenQuestion holds

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LicenceCC BY-NC
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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.