Evidence map›Paper›PMID 37628611›Full record

ArticleGenes2023

High Atlastin 2-2 (ATL2-2) Expression Associates with Worse Prognosis in Estrogen-Receptor-Positive Breast Cancer.

Inga Reynisdottir, Adalgeir Arason, Edda S Freysteinsdottir, Sigrun B Kristjansdottir, Bylgja Hilmarsdottir, Gunnhildur A Traustadottir, Oskar T Johannsson, Bjarni A Agnarsson, Rosa B Barkardottir

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

9 authors at 2 institutions in 1 country.

Inga ReynisdottirCell Biology Unit, Department of Pathology, Landspitali-The National University Hospital of Iceland, 101 Reykjavik, Iceland.ORCID 0000-0002-9730-7476
Adalgeir ArasonBMC (Biomedical Center), Faculty of Medicine, University of Iceland, 101 Reykjavik, Iceland.
Edda S FreysteinsdottirMolecular Pathology Unit, Department of Pathology, Landspitali-The National University Hospital of Iceland, 101 Reykjavik, Iceland.
Sigrun B KristjansdottirDepartment of Pathology, Landspitali-The National University Hospital of Iceland, 101 Reykjavik, Iceland.
Bylgja HilmarsdottirBMC (Biomedical Center), Faculty of Medicine, University of Iceland, 101 Reykjavik, Iceland.
Gunnhildur A TraustadottirBMC (Biomedical Center), Faculty of Medicine, University of Iceland, 101 Reykjavik, Iceland.ORCID 0000-0001-6044-0989
Oskar T JohannssonDepartment of Oncology, Landspitali-The National University Hospital of Iceland, 101 Reykjavik, Iceland.
Bjarni A AgnarssonDepartment of Pathology, Landspitali-The National University Hospital of Iceland, 101 Reykjavik, Iceland.
Rosa B BarkardottirBMC (Biomedical Center), Faculty of Medicine, University of Iceland, 101 Reykjavik, Iceland.
University of Iceland · ISNational University Hospital of Iceland · IS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The disruption of endoplasmic reticulum (ER) homeostasis occurs in many human diseases. Atlastins (ATLs) maintain the branched network of the ER. The dysregulation of ATL2, located at ER network junctions, has been associated with cancer. ATL2 is necessary for lipid droplet formation in murine breast tissue. Thus, we analyzed whether ATL2 has a role in human breast cancer (BC) pathology. The expression of ATL2 variant ATL2-2 was analyzed in breast tumors from the BC cohorts of the TCGA, METABRIC, and two independent Icelandic cohorts, Cohort 1 and 2; its association with clinical, pathological, survival, and cellular pathways was explored. ATL2-2 mRNA and protein expression were higher in breast tumors than in normal tissue. ATL2-2 mRNA associated with tumor characteristics that indicate a worse prognosis. In METABRIC, high ATL2-2 mRNA levels were associated with shorter BC-specific survival (BCSS) in patients with estrogen-receptor-positive luminal breast tumors, which remained significant after correction for grade and tumor size (HR 1.334, CI 1.063-1.673). Tumors with high ATL2 mRNA showed an upregulation of hallmark pathways MYC targets v1, E2F targets, and G2M checkpoint genes. Taken together, the results suggest that high levels of ATL2-2 may support BC progression through key cancer driver pathways.

Indexed as

Breast NeoplasmsAnimalsBreastEstrogensFemaleHumansMicePrognosisRNA, MessengerEstrogensRNA, MessengerATL2ATL2-2Atlastin 2breast cancerendoplasmic reticulumsurvival

Identifiers

PMID37628611
PMCPMC10454310
OpenAlexW4385421863

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.