Evidence map›Paper›PMID 32326116›Full record

ArticleInternational journal of molecular sciences2020

Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells.

Carina Forsare, Pär-Ola Bendahl, Eric Moberg, Charlotte Levin Tykjær Jørgensen, Sara Jansson, Anna-Maria Larsson, Kristina Aaltonen, Lisa Rydén

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  9. Circulating tumor cells: biology and clinical significance.Signal transduction and targeted therapy · 2021
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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 1 institution in 1 country.

Carina ForsareDivision of Oncology, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.
Pär-Ola BendahlDivision of Oncology, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.
Eric MobergDivision of Oncology, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.
Charlotte Levin Tykjær JørgensenDivision of Oncology, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.
Sara JanssonDivision of Oncology, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.
Anna-Maria LarssonDivision of Oncology, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.
Kristina AaltonenDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, SE-223 81 Lund, Sweden.
Lisa RydénDivision of Surgery, Department of Clinical Sciences Lund, Lund University, SE-223 81 Lund, Sweden.ORCID 0000-0001-7515-3130
Lund University · SE

Funding

Biocare-strategic research area at Lund University 2016-124359Governmental Funding of Clinical Research within the National Health Service (ALF) 2018-40304Skåne University Hospital Funds 2017-92502; 2018-92502the Crafoord Foundation 20170702the King Gustav V Jubilee Foundation 19/140141the Mrs Berta Kamprad Foundation 2017-39The Swedish Cancer Society 2016/563; 190388the Swedish Research Council 2015-02516
6 · The paper itself

Abstract

backgroundThe estrogen receptor (ER) can change expression between primary tumor (PT) and distant metastasis (DM) in breast cancer. A tissue biopsy reflects a momentary state at one location, whereas circulating tumor cells (CTCs) reflect real-time tumor progression. We evaluated ER-status during tumor progression from PT to DM and CTCs, and related the ER-status of CTCs to prognosis.

methodsIn a study of metastatic breast cancer, blood was collected at different timepoints. After CellSearch

resultsEvidence of a shift from ER positivity to negativity between PT and DM was demonstrated (

conclusionsA shift in ER-status from PT to DM/CTCs was demonstrated. ER-positive CTCs during systemic therapy might reflect the retention of a favorable phenotype that still responds to therapy.

Indexed as

Biomarkers, TumorAdultAgedAged, 80 and overBreast NeoplasmsDisease ProgressionFemaleFollow-Up StudiesHumansMiddle AgedNeoplasm MetastasisNeoplasmsNeoplasm StagingNeoplastic Cells, CirculatingPrognosisReceptors, EstrogenBiomarkers, TumorReceptors, Estrogenbreast cancercirculating tumor cellsestrogen receptor: tumor progressionmetastasis

Identifiers

PMID32326116
PMCPMC7215368
OpenAlexW3017342205

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.