Evidence map›Paper›PMID 37599786›Full record

ArticleCancer research communications2023

LNS8801 inhibits Acute Myeloid Leukemia by Inducing the Production of Reactive Oxygen Species and Activating the Endoplasmic Reticulum Stress Pathway.

Inyoung Lee, Miriam Doepner, Jillian Weissenrieder, Ariana D Majer, Sophia Mercado, Angela Estell, Christopher A Natale, Pamela J Sung, J Kevin Foskett, Martin P Carroll and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 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
1.2field-weighted citation impact, top 20% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Mitochondrial CaJournal of cellular physiology · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. 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

11 authors at 3 institutions in 1 country.

Inyoung LeeDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-8406-1801
Miriam DoepnerDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-9736-2651
Jillian WeissenriederDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-8096-5421
Ariana D MajerDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-5301-8720
Sophia MercadoDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-0504-493X
Angela EstellDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-3393-8148
Christopher A NataleDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-4949-3849
Pamela J SungDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New Jersey.ORCID 0000-0002-5828-5622
J Kevin FoskettDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-8854-0268
Martin P CarrollDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-5622-3735
Todd W RidkyDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-8482-1284
University of Pennsylvania · USAmicus Therapeutics (United States) · USRoswell Park Comprehensive Cancer Center · US

Funding

Signaling Modulators in Epidermal CarcinogenesisR01CA163566 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RIDKY, TODD W · 2012 to 2016
$1.6M
Improving targeted therapy in FLT3-mutated AMLK08CA230190 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SUNG, PAMELA JEANNETTE · 2020 to 2024
$1.0M
Development of GPER agonists as Cancer TherapeuticsR41CA228695 · NCI · LINNAEUS THERAPEUTICS, LLC · PI RIDKY, TODD W · 2018 to 2018
$300k
Mechanisms by which of GPCR Signaling Inhibits Acute Myeloid LeukemiaF31CA265219 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LEE, IN YOUNG · 2021 to 2022
$80k
NCI NIH HHS F31 CA265219NCI NIH HHS K08 CA230190NCI NIH HHS R01 CA163566NCI NIH HHS R41 CA228695
6 · The paper itself

Abstract

Despite recent therapeutic advances, the 5-year survival rate for adults with acute myeloid leukemia (AML) is poor and standard-of-care chemotherapy is associated with significant toxicity, highlighting the need for new therapeutic approaches. Recent work from our group and others established that the G protein-coupled estrogen receptor (GPER) is tumor suppressive in melanoma and other solid tumors. We performed a preliminary screen of human cancer cell lines from multiple malignancies and found that LNS8801, a synthetic pharmacologic agonist of GPER currently in early phase clinical trials, promoted apoptosis in human AML cells. Using human AML cell lines and primary cells, we show that LNS8801 inhibits human AML in preclinical Significance: Previous work demonstrated that LNS8801 inhibits cancer via GPER activation, especially in solid tumors. Here we show that LNS8801 inhibits AML via GPER-independent mechanisms that include ROS induction and ER activation.

Indexed as

EndoribonucleasesLeukemia, Myeloid, AcuteAdultEndoplasmic Reticulum StressEstrogensHumansProtein Serine-Threonine KinasesReactive Oxygen SpeciesEndoribonucleasesEstrogensProtein Serine-Threonine KinasesReactive Oxygen Species

Identifiers

PMID37599786
PMCPMC10438922
OpenAlexW4385612786

What Socratic 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 Socratic graph.