Evidence map›Paper›PMID 23043150›Full record

ReviewCancer discovery2012

Measuring oncogenic signaling pathways in cancer with PET: an emerging paradigm from studies in castration-resistant prostate cancer.

Michael J Evans

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer discovery, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. A Feasibility Study Showing [Molecular imaging and biology · 2016
    Trial
  2. Article
  3. Review
  4. Article
  5. Noninvasive Measurement of mTORC1 Signaling withClinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  6. 68Ga-PSMA-11 PET Imaging of Response to Androgen Receptor Inhibition: First Human Experience.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2017
    Article
  7. Androgen receptor targeted therapies in castration-resistant prostate cancer: Bench to clinic.International journal of urology : official journal of the Japanese Urological Association · 2016
    Review
  8. Article
  9. Article
  10. Article
  11. Annotating STEAP1 regulation in prostate cancer with 89Zr immuno-PET.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2014
    Article
  12. 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

1 author at 1 institution in 1 country.

Michael J EvansHuman Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA. evansm1@mskcc.org
Memorial Sloan Kettering Cancer Center · US

Funding

Molecular Imaging: Training for OncologyR25CA096945 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI HRICAK, HEDVIG · 2002 to 2013
$5.2M
Noninvasive measurement of oncogenic signaling pathways with 89Zr-transferrinK99CA172695 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI EVANS, MICHAEL JOHN · 2013 to 2013
$91k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA172695NCI NIH HHS R25 CA096945NCI NIH HHS R25-CA096945
6 · The paper itself

Abstract

unlabelledAs parallel advances in cancer biology and drug development continue to elevate the role of targeted therapies in oncology, the need for imaging biomarkers that systematically measure the biology associated with therapeutic intervention has become more urgent. Although the molecular imaging community has a commitment to develop technologies to this end, few investigational radiotracers directly measure the biology of common oncogenic signaling pathways often addressed by targeted therapies. Visible progress has been achieved with a handful of radiotracers rationally designed to intercalate the pathobiology of prostate cancer, a molecularly heterogeneous disease nevertheless broadly defined by a fairly small repertoire of recurrent oncogenic lesions. SIGNIFICANCE: That variable treatment responses or emergent resistance phenotypes are often documented in humans argues strongly for diagnostic technologies that can be realistically applied posttherapy to capture the dynamic patterns of disease response. The purpose of this review is to describe a collection of radiotracers developed to measure the pathobiology of prostate cancer for improved treatment monitoring, placing particular emphasis on the biologic rationale for their preparation. A chronologic description of radiotracer development programs is outlined, primarily to stress how an ongoing dialectic between earlier and more contemporary imaging technologies has accelerated discovery.

Indexed as

RadiopharmaceuticalsAndrogen AntagonistsHumansMaleNeoplasms, Hormone-DependentPositron-Emission TomographyProstatic NeoplasmsSignal TransductionAndrogen AntagonistsRadiopharmaceuticals

Identifiers

PMID23043150
PMCPMC3508522
OpenAlexW2130611299

What OpenQuestion holds

Textmetadata
LicenceTDM
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.