Evidence map›Paper›PMID 34637026›Full record

ReviewEJNMMI research2021

Rationale for MYC imaging and targeting in pancreatic cancer.

Günter Schneider, Matthias Wirth, Ulrich Keller, Dieter Saur

Open access · goldAbstract readReview
In one paragraph

Review in EJNMMI research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

4 authors at 1 institution in 2 countries.

Günter Schneider *Medical Clinic and Policlinic II, Klinikum Rechts Der Isar, TU Munich, 81675, Munich, Germany. guenter.schneider@med.uni-goettingen.de.ORCID http://orcid.org/0000-0003-1840-4508
Matthias Wirth *German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), 69120, Heidelberg, Germany. matthias.wirth@charite.de.
Ulrich KellerGerman Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), 69120, Heidelberg, Germany.
Dieter SaurGerman Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), 69120, Heidelberg, Germany.
German Cancer Research Center · DE

Funding

Deutsche Forschungsgemeinschaft DFG-SCHN959/3-2Deutsche Forschungsgemeinschaft SCHN959/3-2Deutsche Forschungsgemeinschaft SCHN959/6-1Deutsche Forschungsgemeinschaft SFB824Deutsche Krebshilfe 70113760Deutsche Krebshilfe 70114425Stiftung Charite UKWilhelm Sander-Stiftung 70113760Wilhelm Sander-Stiftung 70114425
6 · The paper itself

Abstract

The incidence and lethality of pancreatic ductal adenocarcinoma (PDAC) will continue to increase in the next decade. For most patients, chemotherapeutic combination therapies remain the standard of care. The development and successful implementation of precision oncology in other gastrointestinal tumor entities point to opportunities also for PDAC. Therefore, markers linked to specific therapeutic responses and important subgroups of the disease are needed. The MYC oncogene is a relevant driver in PDAC and is linked to drug resistance and sensitivity. Here, we update recent insights into MYC biology in PDAC, summarize the connections between MYC and drug responses, and point to an opportunity to image MYC non-invasively. In sum, we propose MYC-associated biology as a basis for the development of concepts for precision oncology in PDAC.

Indexed as

MYCPancreatic cancerPrecision oncologyTargeted therapies

Identifiers

PMID34637026
PMCPMC8511206
OpenAlexW3205530759

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.