Evidence map›Paper›PMID 35575456›Full record

ArticleeLife2022

Stereospecific lasofoxifene derivatives reveal the interplay between estrogen receptor alpha stability and antagonistic activity in

David J Hosfield, Sandra Weber, Nan-Sheng Li, Madline Sauvage, Carstyn F Joiner, Govinda R Hancock, Emily A Sullivan, Estelle Ndukwe, Ross Han, Sydney Cush and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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  16. PARP-1 as a novel target in endocrine-resistant breast cancer.Journal of experimental & clinical cancer research : CR · 2025
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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

14 authors at 3 institutions in 2 countries.

David J HosfieldBen May Department for Cancer Research, University of Chicago, Chicago, United States.
Sandra WeberInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Nan-Sheng LiBen May Department for Cancer Research, University of Chicago, Chicago, United States.
Madline SauvageInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Carstyn F JoinerDepartment of Cancer Biology, Loyola University Chicago, Maywood, United States.
Govinda R HancockDepartment of Cancer Biology, Loyola University Chicago, Maywood, United States.
Emily A SullivanDepartment of Cancer Biology, Loyola University Chicago, Maywood, United States.
Estelle NdukweBen May Department for Cancer Research, University of Chicago, Chicago, United States.
Ross HanBen May Department for Cancer Research, University of Chicago, Chicago, United States.
Sydney CushBen May Department for Cancer Research, University of Chicago, Chicago, United States.
Muriel LainéBen May Department for Cancer Research, University of Chicago, Chicago, United States.
Sylvie C MaderInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Geoffrey L GreeneBen May Department for Cancer Research, University of Chicago, Chicago, United States.ORCID 0000-0001-6894-8728
Sean W FanningDepartment of Cancer Biology, Loyola University Chicago, Maywood, United States.ORCID 0000-0002-9428-0060
University of Chicago · USLoyola University Chicago · USInstitute for Research in Immunology and Cancer · CA

Funding

CIHR
6 · The paper itself

Abstract

Chemical manipulation of estrogen receptor alpha ligand binding domain structural mobility tunes receptor lifetime and influences breast cancer therapeutic activities. Selective estrogen receptor modulators (SERMs) extend estrogen receptor alpha (ERα) cellular lifetime/accumulation. They are antagonists in the breast but agonists in the uterine epithelium and/or in bone. Selective estrogen receptor degraders/downregulators (SERDs) reduce ERα cellular lifetime/accumulation and are pure antagonists. Activating somatic

Indexed as

Breast NeoplasmsEstrogen AntagonistsEstrogen Receptor alphaFemaleHumansLigandsMutationPyrrolidinesSelective Estrogen Receptor ModulatorsTetrahydronaphthalenesESR1 protein, humanEstrogen AntagonistsEstrogen Receptor alphaLasofoxifeneLigandsPyrrolidinesSelective Estrogen Receptor ModulatorsTetrahydronaphthalenesantiestrogenbiochemistrybreast cancercancer biologychemical biologyD538G ESR1 Mutationdrug resistanceE. coliestrogen receptor degradationhormone resistancehumanY537S ESR1 Mutation

Identifiers

PMID35575456
PMCPMC9177151
OpenAlexW4280516872

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.