Evidence map›Paper›PMID 28926977›Full record

ArticleInternational journal of molecular sciences2017

Mouse Monoclonal Antibodies Generated from Full Length Human Cereblon: Detection of Cereblon Protein in Patients with Multiple Myeloma.

Xiubao Chang, Qinqin Xu, Yuexian Hou, Cynthia Li, Ye Xu, A Keith Stewart

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. 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

6 authors at 1 institution in 1 country.

Xiubao ChangDepartment of Biochemistry & Molecular Biology, College of Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. xbchang@mayo.edu.
Qinqin XuDepartment of Biochemistry & Molecular Biology, College of Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. Xu.Qinqin@mayo.edu.
Yuexian HouDepartment of Biochemistry & Molecular Biology, College of Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. hou.yue@mayo.edu.
Cynthia LiDepartment of Biochemistry & Molecular Biology, College of Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. csl95@cornell.edu.
Ye XuDepartment of Biochemistry & Molecular Biology, College of Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. xuye@bjmu.edu.cn.
A Keith StewartDivision of Hematology, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. stewart.keith@mayo.edu.
Mayo Clinic in Arizona · US

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
The Role of Cereblon Pathways in MyelomaR01CA183968 · NCI · MAYO CLINIC ARIZONA · PI KUMAR, SHAJI KUNNATHU, STEWART, ALEXANDER KEITH · 2014 to 2018
$2.3M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA183968
6 · The paper itself

Abstract

Immunomodulatory drugs (IMiDs) are profoundly active compounds in the treatment of patients with multiple myeloma (MM). However, despite the fact that treatment with IMiDs has dramatically improved survival for patients with MM, the majority of MM patients develop IMiDs resistance over time. We have found that expression of functional cereblon is required for IMiDs' action. In addition, it has been reported that cells expressing high levels of cereblon are resistant to proteasome inhibitor, implying that patients with high levels of cereblon should be resistant to proteasome inhibitor. If the above conclusions are correct, cereblon could be considered as a biomarker to determine which standard regimens should be used to treat patients with MM. Unfortunately, the conclusions mentioned above have not been clinically confirmed. In order to confirm these conclusions, we have generated three highly specific mouse monoclonal antibodies (mAbs) against full-length human cereblon. These mAbs can be used to do western blot, immunoprecipitation and immunohistochemistry staining. In addition, their epitopes have been precisely determined and the peptides covering their epitopes completely blocked the antibody binding to cereblon in western blot analysis or in immunohistochemistry staining of MM patients' specimens.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAntibodies, MonoclonalAntibody AffinityCell Line, TumorHumansImmunologic FactorsMiceMultiple MyelomaPeptide HydrolasesUbiquitin-Protein LigasesAdaptor Proteins, Signal TransducingAntibodies, MonoclonalCRBN protein, humanImmunologic FactorsPeptide HydrolasesUbiquitin-Protein Ligasescereblon (CRBN)epitopeimmunohistochemistry (IHC) stainingimmunomodulatory drugs (IMiDs)immunoprecipitationmonoclonal antibody (mAb)multiple myeloma (MM)

Identifiers

PMID28926977
PMCPMC5618648
OpenAlexW2754784131

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.