Evidence map›Paper›PMID 40356407›Full record

ArticleFuture oncology (London, England)2025

A genome-wide association study using HapMap cell lines reveals modulators of cellular response to cyclophosphamide.

Mohammed O Gbadamosi, Neha Bhise, Taraswi Mitra Ghosh, Elizabeth K Molchan, Kathleen Streeks, Jason Puglise, Alyssa Ohaegbulam, Mariana Makarem, Oluwaseyi Olabige, Changlin Yang and 4 more

Abstract read
In one paragraph

Article in Future oncology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Mohammed O GbadamosiDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.ORCID 0000-0002-2751-1172
Neha BhiseDepartment of Experimental & Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, MN, USA.
Taraswi Mitra GhoshDepartment of Experimental & Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, MN, USA.
Elizabeth K MolchanDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.ORCID 0009-0004-4501-5609
Kathleen StreeksDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.
Jason PugliseDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.
Alyssa OhaegbulamDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.
Mariana MakaremDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.
Oluwaseyi OlabigeDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.
Changlin YangDepartment of Neurosurgery, Brain Tumor Immunotherapy Program, Preston A. Wells Jr. Center for Brain Tumor Therapy, University of Florida, Gainesville, FL, USA.
Luisel Ricks-SantiDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.
Duane A MitchellDepartment of Neurosurgery, Brain Tumor Immunotherapy Program, Preston A. Wells Jr. Center for Brain Tumor Therapy, University of Florida, Gainesville, FL, USA.
Brooke L FridleyDivision of Health Services and Outcomes Research, Children's Mercy, Kansas City, MO, USA.
Jatinder K LambaDepartment of Pharmacotherapy and Translational Research, College of Pharmacy, Gainesville, FL, USA.

Funding

University of Florida Health Cancer Center Support GrantP30CA247796 · NCI · UNIVERSITY OF FLORIDA · PI Christian Jobin · 2023 to 2026
$10.9M
Pharmacogenomics of Ara-C in AMLR01CA132946 · NCI · UNIVERSITY OF MINNESOTA · PI LAMBA, JATINDER K., POUNDS, STANLEY BARRETT · 2008 to 2025
$5.3M
Training Program for Applied Research and Development in Genomic MedicineT32HG008958 · NHGRI · UNIVERSITY OF FLORIDA · PI Larisa Humma Cavallari, Stephen E. Kimmel · 2018 to 2026
$3.8M
Decoding the Heterogeneity in Chemo-Immunomodulation to Unlock the Potential of Chemoimmunotherapy in Metastatic Triple-Negative Breast CancerDP5OD036134 · OD · UNIVERSITY OF FLORIDA · PI Mohammed Olusoji Gbadamosi · 2023 to 2026
$1.9M
NCI NIH HHS P30 CA247796NCI NIH HHS R01 CA132946NHGRI NIH HHS T32 HG008958NIH HHS DP5 OD036134
6 · The paper itself

Abstract

aimsThis study identifies single-nucleotide polymorphisms (SNPs) associated with cellular response to cyclophosphamide (CTX) using phosphoramide mustard (PM), its primary cytotoxic metabolite, and explores the downstream consequences for breast cancer (BC) patients.

methodsWe analyzed 1,978,545 SNPs from EBV-transformed lymphoblastic cell lines (LCLs) derived from 53 unrelated European individuals, in a genome-wide association study using cellular PM sensitivity data. We filtered SNPs associated with PM sensitivity (

resultsTwenty SNPs were filtered out including rs12408401, which was associated with PM resistance (

conclusionOur study identifies SNPs significantly associated with cellular CTX response with potential mechanistic and clinical relevance, thereby providing insights toward optimized CTX treatment strategies.

Indexed as

Antineoplastic Agents, AlkylatingBreast NeoplasmsCyclophosphamideDrug Resistance, NeoplasmPolymorphism, Single NucleotideCell Line, TumorFemaleGene Expression Regulation, NeoplasticGenome-Wide Association StudyHapMap ProjectHumansPhosphoramide MustardsAntineoplastic Agents, AlkylatingCyclophosphamidePhosphoramide Mustardsbreast cancerCyclophosphamideHapMappharmacodynamicspharmacogenomicsSNPs

Identifiers

PMID40356407
PMCPMC12150645

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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.