Evidence map›Paper›PMID 38275056›Full record

ReviewCurrent cancer drug targets2024

Bromodomain Protein-directed Agents and MYC in Small Cell Lung Cancer.

Gerhard Hamilton, Sandra Stickler, Barbara Rath

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current cancer drug targets, 2024. 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
1.4field-weighted citation impact, top 21% 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. Article
  2. Review
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 at 1 institution in 1 country.

Gerhard HamiltonInstitute of Pharmacology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-4038-5182
Sandra SticklerInstitute of Pharmacology, Medical University of Vienna, Vienna, Austria.
Barbara RathInstitute of Pharmacology, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small cell lung cancer (SCLC) has a dismal prognosis. In addition to the inactivation of the tumor suppressors TP53 and RB1, tumor-promoting MYC and paralogs are frequently overexpressed in this neuroendocrine carcinoma. SCLC exhibits high resistance to second-line chemotherapy and all attempts of novel drugs and targeted therapy have failed so far to achieve superior survival. MYC and paralogs have key roles in the oncogenic process, orchestrating proliferation, apoptosis, differentiation, and metabolism. In SCLC, MYC-L and MYC regulate the neuroendocrine dedifferentiation of SCLC cells from Type A (ASCL1 expression) to the other SCLC subtypes. Targeting MYC to suppress tumor growth is difficult due to the lack of suitable binding pockets and the most advanced miniprotein inhibitor Omomyc exhibits limited efficacy. MYC may be targeted indirectly

Indexed as

Antineoplastic AgentsLung NeoplasmsProto-Oncogene Proteins c-mycSmall Cell Lung CarcinomaAnimalsCell Cycle ProteinsHumansMolecular Targeted TherapyTranscription FactorsAntineoplastic AgentsCell Cycle ProteinsMYC protein, humanProto-Oncogene Proteins c-mycTranscription FactorsBET inhibitorsbromodomain proteinsDNA damage response (DDR).MYC paralogsPROTACSmall cell lung cancer

Identifiers

PMID38275056
OpenAlexW4391231397

What Socratic holds

Textmetadata
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 Socratic graph.