Evidence map›Paper›PMID 35646666›Full record

ArticleFrontiers in oncology2022

Single-Cell Proteomics and Tumor RNAseq Identify Novel Pathways Associated With Clofazimine Sensitivity in PI- and IMiD- Resistant Myeloma, and Putative Stem-Like Cells.

Harish Kumar, Suman Mazumder, Neeraj Sharma, Sayak Chakravarti, Mark D Long, Nathalie Meurice, Joachim Petit, Song Liu, Marta Chesi, Sabyasachi Sanyal and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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

17 authors at 6 institutions in 2 countries.

Harish KumarDepartment of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, AL, United States.
Suman MazumderDepartment of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, AL, United States.
Neeraj SharmaDivision of Laboratory Genetics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.
Sayak ChakravartiDepartment of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, AL, United States.
Mark D LongDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.
Nathalie MeuriceDivision of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Joachim PetitDivision of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Song LiuDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.
Marta ChesiDivision of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Sabyasachi SanyalBiochemistry Division, CSIR-Central Drug Research Institute, Lucknow, India.
A Keith StewartDivision of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Shaji KumarDivision of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, United States.
Leif BergsagelDivision of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
S Vincent RajkumarDivision of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, United States.
Linda B BaughnDivision of Laboratory Genetics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.
Brian G Van NessDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, United States.
Amit Kumar MitraDepartment of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, AL, United States.
Mayo Clinic in Arizona · USAuburn University · USMayo Clinic · USRoswell Park Comprehensive Cancer Center · USCentral Drug Research Institute · INUniversity of Minnesota · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel · 2015 to 2026
$25.5M
Project 3 - Modeling Proteasome Inhibitor Response and Resistance in Cell Lines and Patient Samples with Single Cell Analysis of SubpopulationsU54CA224018 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2017 to 2021
$6.0M
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA186781NCI NIH HHS U54 CA224018
6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable plasma cell malignancy with dose-limiting toxicities and inter-individual variation in response/resistance to the standard-of-care/primary drugs, proteasome inhibitors (PIs), and immunomodulatory derivatives (IMiDs). Although newer therapeutic options are potentially highly efficacious, their costs outweigh the effectiveness. Previously, we have established that clofazimine (CLF) activates peroxisome proliferator-activated receptor-γ, synergizes with primary therapies, and targets cancer stem-like cells (CSCs) in drug-resistant chronic myeloid leukemia (CML) patients. In this study, we used a panel of human myeloma cell lines as

Indexed as

clofazimineCyTOFhuman myeloma cell lines (HMCLs)immunomodulatory drugs (IMiDs)myelomaproteasome inhibitors (PI)RNAseqside population (SP)

Identifiers

PMID35646666
PMCPMC9130773
OpenAlexW4280643329

What OpenQuestion 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 OpenQuestion graph.