Evidence map›Paper›PMID 38114522›Full record

ArticleNPJ breast cancer2023

Endoxifen downregulates AKT phosphorylation through protein kinase C beta 1 inhibition in ERα+ breast cancer.

Swaathi Jayaraman, Xinyan Wu, Krishna R Kalari, Xiaojia Tang, Mary J Kuffel, Elizabeth S Bruinsma, Shahrzad Jalali, Kevin L Peterson, Cristina Correia, Rachel A Kudgus and 10 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A Hypothesized Therapeutic Role of (Z)-Endoxifen in Duchenne Muscular Dystrophy (DMD).Degenerative neurological and neuromuscular disease · 2025
    Article
  6. Review
  7. Article
  8. Review
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

20 authors at 3 institutions in 1 country.

Swaathi Jayaraman *Department of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Xinyan Wu *Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Krishna R KalariDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
Xiaojia TangDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
Mary J KuffelDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Elizabeth S BruinsmaDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0002-7938-438X
Shahrzad JalaliDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Kevin L PetersonDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Cristina CorreiaDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Rachel A KudgusDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Scott H KaufmannDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0002-4900-7145
Santosh RenuseDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
James N IngleDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0003-1257-7731
Joel M ReidDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Matthew M AmesDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Alan P FieldsDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL, 32224, USA.
Matthew J SchellenbergDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0001-7036-5943
John R HawseDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0003-3406-470X
Akhilesh PandeyDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0001-9943-6127
Matthew P GoetzDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA. Goetz.Matthew@mayo.edu.ORCID 0000-0002-4383-270X
Mayo Clinic in Arizona · USMayo Clinic · USMayo Clinic in Florida · US

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI Fergus Joseph Couch · 2005 to 2026
$49.9M
NCI NIH HHS P50 CA116201
6 · The paper itself

Abstract

Endoxifen, a secondary tamoxifen metabolite, is a potent antiestrogen exhibiting estrogen receptor alpha (ERα) binding at nanomolar concentrations. Phase I/II clinical trials identified clinical activity of Z-endoxifen (ENDX), in endocrine-refractory metastatic breast cancer as well as ERα+ solid tumors, raising the possibility that ENDX may have a second, ERα-independent, mechanism of action. An unbiased mass spectrometry approach revealed that ENDX concentrations achieved clinically with direct ENDX administration (5 µM), but not low concentrations observed during tamoxifen treatment (<0.1 µM), profoundly altered the phosphoproteome of the aromatase expressing MCF7AC1 cells with limited impact on the total proteome. Computational analysis revealed protein kinase C beta (PKCβ) and protein kinase B alpha or AKT1 as potential kinases responsible for mediating ENDX effects on protein phosphorylation. ENDX more potently inhibited PKCβ1 kinase activity compared to other PKC isoforms, and ENDX binding to PKCβ1 was confirmed using Surface Plasma Resonance. Under conditions that activated PKC/AKT signaling, ENDX induced PKCβ1 degradation, attenuated PKCβ1-activated AKT

Identifiers

PMID38114522
PMCPMC10730845
OpenAlexW4389949257

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.