Evidence map›Paper›PMID 36772966›Full record

ArticleThe oncologist2023

Therapeutic Role of Tamoxifen for Triple-Negative Breast Cancer: Leveraging the Interaction Between ERβ and Mutant p53.

Lauren Scarpetti, Chetan C Oturkar, Dejan Juric, Maria Shellock, Giuliana Malvarosa, Kathryn Post, Steven Isakoff, Nancy Wang, Brian Nahed, Kevin Oh and 2 more

Open access · goldAbstract read
In one paragraph

Article in The oncologist, 2023. 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
4.1field-weighted citation impact, top 6% 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, 13 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

12 authors at 2 institutions in 1 country.

Lauren ScarpettiMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-7642-0461
Chetan C OturkarRoswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Dejan JuricMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Maria ShellockMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Giuliana MalvarosaMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Kathryn PostMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Steven IsakoffMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Nancy WangMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Brian NahedMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Kevin OhMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Gokul M DasRoswell Park Comprehensive Cancer Center, Buffalo, NY, USA.ORCID 0000-0003-2937-8093
Aditya BardiaMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-4885-1157
Harvard University · USRoswell Park Comprehensive Cancer Center · US

Funding

Functional Significance of individual p53 mutations in determining the role of estrogen receptor beta in triple negative breast cancerR01CA251545 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI DAS, GOKUL M. · 2021 to 2025
$2.9M
P53 AND ESTROGEN IN PCNA EXPRESSION OSTEOSARCOMA CELLSR01CA079911 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI DAS, GOKUL M · 1999 to 2003
$963k
Role of Estrogen Receptor alpha-p53 Interaction in Resistance to Tamoxifen TherapR21CA137635 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI DAS, GOKUL M., KULKARNI, SWATI · 2009 to 2010
$647k
NCI NIH HHS R01 CA079911NCI NIH HHS R01 CA251545NCI NIH HHS R21 CA137635
6 · The paper itself

Abstract

The absence of effective therapeutic targets and aggressive nature of triple-negative breast cancer (TNBC) renders this disease subset difficult to treat. Although estrogen receptor beta (ERβ) is expressed in TNBC, studies on its functional role have yielded inconsistent results. However, recently, our preclinical studies, along with other observations, have shown the potential therapeutic utility of ERβ in the context of mutant p53 expression. The current case study examines the efficacy of the selective estrogen receptor modulator tamoxifen in p53-mutant TNBC with brain metastases. Significant increase in ERβ protein expression and anti-proliferative interaction between mutant p53 and ERβ were observed after cessation of tamoxifen therapy, with significant regression of brain metastases. This case study provides supporting evidence for the use of tamoxifen in p53-mutant, ERβ+TNBC, especially in the setting of brain metastasis.

Indexed as

Breast NeoplasmsTriple Negative Breast NeoplasmsCell Line, TumorEstrogen Receptor alphaEstrogen Receptor betaFemaleHumansTamoxifenTumor Suppressor Protein p53Estrogen Receptor alphaEstrogen Receptor betaTamoxifenTP53 protein, humanTumor Suppressor Protein p53brain metastasisestrogen receptor βmutant p53proximity ligation assay (PLA)tamoxifentriple-negative breast cancer

Identifiers

PMID36772966
PMCPMC10078911
OpenAlexW4320033160

What OpenQuestion holds

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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.