Evidence map›Paper›PMID 36900259›Full record

ArticleCancers2023

NSC243928 Treatment Induces Anti-Tumor Immune Response in Mouse Mammary Tumor Models.

Benson Chellakkan Selvanesan, Alvaro de Mingo Pulido, Sheelu Varghese, Deepak Rohila, Daniel Hupalo, Yuriy Gusev, Sara Contente, Matthew D Wilkerson, Clifton L Dalgard, Geeta Upadhyay

Open access · goldFull text read
In one paragraph

Article in Cancers, 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
1.0field-weighted citation impact, top 23% 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, 6 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

10 authors at 4 institutions in 1 country.

Benson Chellakkan SelvanesanDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Alvaro de Mingo PulidoMoffitt Cancer Center, 12902 Magnolia Drive, Tampa, FL 33612, USA.
Sheelu VargheseDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Deepak RohilaDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.ORCID 0000-0001-7138-2702
Daniel HupaloHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Yuriy GusevInnovation Center for Biomedical Informatics, Department of Oncology, Georgetown University Medical Center, Washington, DC 20057, USA.ORCID 0000-0001-7371-4715
Sara ContenteDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.ORCID 0000-0002-8099-2817
Matthew D WilkersonDepartment of Anatomy, Physiology, and Genetics, Center for Military Precision Health, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Clifton L DalgardDepartment of Anatomy, Physiology, and Genetics, Center for Military Precision Health, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Geeta UpadhyayDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.ORCID 0000-0002-7635-8194
Henry M. Jackson Foundation · USUniformed Services University of the Health Sciences · USGeorgetown University · USMoffitt Cancer Center · US

Funding

Role of Ly6K in TGF-beta and immune escape pathways of triple negative breast cancerR01CA227694 · NCI · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI Geeta Upadhyay · 2018 to 2026
$2.4M
Use of Ly6K specific CAR T-cells to treat primary and metastatic triple negative breast cancerR21CA256424 · NCI · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI UPADHYAY, GEETA · 2021 to 2022
$389k
CSR NIH HHS R01CA227694CSR NIH HHS R21CA256424NCI NIH HHS R01 CA227694NCI NIH HHS R21 CA256424
6 · The paper itself

Abstract

NSC243928 induces cell death in triple-negative breast cancer cells in a LY6K-dependent manner. NSC243928 has been reported as an anti-cancer agent in the NCI small molecule library. The molecular mechanism of NSC243928 as an anti-cancer agent in the treatment of tumor growth in the syngeneic mouse model has not been established. With the success of immunotherapies, novel anti-cancer drugs that may elicit an anti-tumor immune response are of high interest in the development of novel drugs to treat solid cancer. Thus, we focused on studying whether NSC243928 may elicit an anti-tumor immune response in the in vivo mammary tumor models of 4T1 and E0771. We observed that NSC243928 induced immunogenic cell death in 4T1 and E0771 cells. Furthermore, NSC243928 mounted an anti-tumor immune response by increasing immune cells such as patrolling monocytes, NKT cells, B1 cells, and decreasing PMN MDSCs in vivo. Further studies are required to understand the exact mechanism of NSC243928 action in inducing an anti-tumor immune response in vivo, which can be used to determine a molecular signature associated with NSC243928 efficacy. NSC243928 may be a good target for future immuno-oncology drug development for breast cancer.

Indexed as

4T1B1 cellsE0771LY6Kmammary tumor modelmyeloid derived suppressor cellsNKT cellsNSC243928

Identifiers

PMID36900259
PMCPMC10000927
OpenAlexW4322503438

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read18
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.