Evidence map›Paper›PMID 23734634›Full record

ReviewJournal of medicinal chemistry2013

The σ2 receptor: a novel protein for the imaging and treatment of cancer.

Robert H Mach, Chenbo Zeng, William G Hawkins

Abstract readReview
In one paragraph

Review in Journal of medicinal chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
–field-weighted citation impact
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

68 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Development of Fluorescent 4-[4-(3Journal of medicinal chemistry · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. σScientific reports · 2022
    Article
  16. Review
  17. Neuroprotective Effects of σACS chemical neuroscience · 2022
    Article
  18. Article
  19. Screening of σJournal of medicinal chemistry · 2022
    Article
  20. Article

8 more citing papers are in PubMed but not listed here.

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

3 authors.

Robert H MachMallinckrodt Institute of Radiology and ‡Department of Surgery, Washington University School of Medicine , St. Louis, Missouri 63110, United States.
Chenbo Zeng
William G Hawkins

Funding

SURGICAL ONCOLOGY TRAINING GRANTT32CA009621 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN, William E. Gillanders · 1988 to 2026
$12.9M
SIGMA-2/PEPTIDOMIMETIC CONJUGATES TARGET APOPTOSIS IN PANCREATIC CANCERR01CA163764 · NCI · WASHINGTON UNIVERSITY · PI HAWKINS, WILLIAM G, SPITZER, DIRK M. · 2012 to 2021
$3.7M
PET Imaging of Breast Cancer via Sigma-2 ReceptorsR33CA102869 · NCI · WASHINGTON UNIVERSITY · PI MACH, ROBERT H · 2004 to 2006
$1.3M
ON THE TRAIL TO PANCREAS CANCER-SELECTIVE TUMOR CELL DEATH (APOPTOSIS)R21CA150945 · NCI · WASHINGTON UNIVERSITY · PI HAWKINS, WILLIAM G · 2010 to 2011
$358k
PET Imaging of Breast Cancer via Sigma-2 ReceptorsR21CA102869 · NCI · WASHINGTON UNIVERSITY · PI MACH, ROBERT H · 2003 to 2003
$192k
SIGMA 1 RECEPTOR PROBES FOR IMAGING TUMOR PROLIFERATIONR41CA081825 · NCI · ANASAZI BIOMEDICAL RESEARCH, INC. · PI MACH, ROBERT H · 1999 to 2000
$105k
RADIOLABELED TROPANE ANALOGS FOR IMAGING BREAST CANCERR41CA080452 · NCI · ANASAZI BIOMEDICAL RESEARCH, INC. · PI MACH, ROBERT H · 1999 to 1999
–
NCI NIH HHS CA102869NCI NIH HHS CA80452NCI NIH HHS CA81825NCI NIH HHS R01 CA163764NCI NIH HHS R21 CA102869NCI NIH HHS R21 CA150945NCI NIH HHS R33 CA102869NCI NIH HHS T32 CA009621
6 · The paper itself

Abstract

The σ2 receptor is an important target for the development of molecular probes in oncology because of its 10-fold higher density in proliferating tumor cells compared with that in quiescent tumor cells and because of the observation that σ2 receptor agonists are able to kill tumor cells via apoptotic and nonapoptotic mechanisms. Although recent evidence indicates that the σ2 receptor binding site is localized within the progesterone receptor membrane component 1 (PGRMC1), most information regarding this protein has been obtained using either radiolabeled or fluorescent receptor-based probes and from biochemical analysis of the effect of σ2 selective ligands on cells grown in culture. This article reviews the development of σ2 receptor ligands and presents an overview of how they have been used in vitro and in vivo to increase our understanding of the role of the σ2 receptor in cancer and proliferation.

Indexed as

AnimalsCell ProliferationDrug DiscoveryHumansMolecular ImagingMolecular ProbesNeoplasmsReceptors, sigmaMolecular ProbesReceptors, sigma

Identifiers

PMID23734634
PMCPMC4064612

What OpenQuestion holds

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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.