Evidence map›Paper›PMID 34400617›Full record

ArticleCell death discovery2021

LIF/LIFR oncogenic signaling is a novel therapeutic target in endometrial cancer.

Weiwei Tang, Kumaraguruparan Ramasamy, Sureshkumar M A Pillai, Bindu Santhamma, Swapna Konda, Prabhakar Pitta Venkata, Logan Blankenship, Junhao Liu, Zexuan Liu, Kristin A Altwegg and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 35 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

20 authors at 4 institutions in 2 countries.

Weiwei TangDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Kumaraguruparan RamasamyDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Sureshkumar M A PillaiDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Bindu SanthammaEvestra, Inc., San Antonio, TX, 78245, USA.
Swapna KondaEvestra, Inc., San Antonio, TX, 78245, USA.
Prabhakar Pitta VenkataDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Logan BlankenshipDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.ORCID http://orcid.org/0000-0002-6934-0236
Junhao LiuDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Zexuan LiuDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Kristin A AltweggDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Behnam EbrahimiDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Uday P PratapDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Xiaonan LiDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Philip T ValenteDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Edward KostDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Gangadhara R SareddyDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Ratna K VadlamudiDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Hareesh B NairEvestra, Inc., San Antonio, TX, 78245, USA.
Rajeshwar R TekmalDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA.
Suryavathi ViswanadhapalliDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX, 78229, USA. viswanadhapa@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · USEvestra (United States) · USCentral South University · CNNanjing University of Chinese Medicine · CN

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Therapeutic agents targeting nuclear receptor signaling in distinct molecular subtypes of breast cancerR01CA223828 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RAJ, GANESH V, VADLAMUDI, RATNA K · 2018 to 2022
$3.0M
FoXM1 inhibition: a novel therapeutic avenue to treat breast cancersR01CA239227 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RAO, MANJEET KUMAR, VADLAMUDI, RATNA K · 2020 to 2024
$2.1M
Development of Small Molecule Inhibitor of PELP1 for Treating Advanced Breast CancerF31CA257298 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ALTWEGG, KRISTIN ANN · 2021 to 2022
$51k
NCI NIH HHS F31 CA257298NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA239227
6 · The paper itself

Abstract

Endometrial cancer (EC) is the fourth most common cancer in women. Advanced-stage EC has limited treatment options with a poor prognosis. There is an unmet need for the identification of actionable drivers for the development of targeted therapies in EC. Leukemia inhibitory factor receptor (LIFR) and its ligand LIF play a major role in cancer progression, metastasis, stemness, and therapy resistance. However, little is known about the functional significance of the LIF/LIFR axis in EC progression. In this study using endometrial tumor tissue arrays, we identified that expression of LIF, LIFR is upregulated in EC. Knockout of LIFR using CRISPR/Cas9 in two different EC cells resulted in a significant reduction of their cell viability and cell survival. In vivo studies demonstrated that LIFR-KO significantly reduced EC xenograft tumor growth. Treatment of established and primary patient-derived EC cells with a novel LIFR inhibitor, EC359 resulted in the reduction of cell viability with an IC

Identifiers

PMID34400617
PMCPMC8367961
OpenAlexW3195151704

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Registered trials

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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.