Evidence map›Paper›PMID 34160558›Full record

ReviewThe Journal of cell biology2021

The long journey to bring a Myc inhibitor to the clinic.

Jonathan R Whitfield, Laura Soucek

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 97 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

2 authors at 2 institutions in 1 country.

Jonathan R WhitfieldVall d'Hebron Institute of Oncology, Edifici Cellex, Barcelona, Spain.ORCID 0000-0002-4925-7283
Laura SoucekVall d'Hebron Institute of Oncology, Edifici Cellex, Barcelona, Spain.ORCID 0000-0002-4750-7971
Institució Catalana de Recerca i Estudis Avançats · ESVall d'Hebron Institute of Oncology · ES

Funding

CIHR PJT-159767
6 · The paper itself

Abstract

The oncogene Myc is deregulated in the majority of human tumors and drives numerous hallmarks of cancer. Despite its indisputable role in cancer development and maintenance, Myc is still undrugged. Developing a clinical inhibitor for Myc has been particularly challenging owing to its intrinsically disordered nature and lack of a binding pocket, coupled with concerns regarding potentially deleterious side effects in normal proliferating tissues. However, major breakthroughs in the development of Myc inhibitors have arisen in the last couple of years. Notably, the direct Myc inhibitor that we developed has just entered clinical trials. Celebrating this milestone, with this Perspective, we pay homage to the different strategies developed so far against Myc and all of the researchers focused on developing treatments for a target long deemed undruggable.

Indexed as

Drug DesignAnimalsAntineoplastic AgentsCell ProliferationDiffusion of InnovationGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyNeoplasmsProto-Oncogene Proteins c-mycSignal TransductionAntineoplastic AgentsMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID34160558
PMCPMC8240852
OpenAlexW3175559262

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.