Evidence map›Paper›PMID 30510014›Full record

ArticleCancer discovery2018

Unleashing Blocked Apoptosis in Cancer Cells: New MCL1 Inhibitors Find Their Groove.

Brian Leber, Justin Kale, David W Andrews

Abstract readComment
PubMed Publisher
In one paragraph

Article in Cancer discovery, 2018. 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
0.3field-weighted citation impact, top 42% 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. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Brian LeberDepartments of Biochemistry and Biomedical Sciences, and Medicine, McMaster University, Hamilton, Ontario, Canada.
Justin KaleBiological Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
David W AndrewsBiological Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada. David.Andrews@sri.utoronto.ca.ORCID 0000-0002-9266-7157
Sunnybrook Health Science Centre · CAMcMaster University · CA

Funding

CIHR FRN12517
6 · The paper itself

Abstract

Unleashing blocked apoptosis has emerged as an important tool in treating cancer as shown by the recent success of the BCL2 inhibitor venetoclax. However, MCL1 represents another important target as it is the predominant survival signal in many types of cancers and functions as a resistance mechanism to BCL2 inhibition. Caenepeel and colleagues and Ramsey and colleagues have developed two novel, potent, and selective MCL1 inhibitors that are effective against many hematologic malignancies, and Nangia and colleagues describe how one of these inhibitors can be successfully combined with BCL-xL and MEK inhibition to treat KRAS-mutated lung cancer.

Indexed as

ApoptosisLeukemia, Myeloid, AcuteBridged Bicyclo Compounds, HeterocyclicCell Line, TumorHumansMyeloid Cell Leukemia Sequence 1 ProteinSulfonamidesBridged Bicyclo Compounds, HeterocyclicMCL1 protein, humanMyeloid Cell Leukemia Sequence 1 ProteinSulfonamidesvenetoclax

Identifiers

PMID30510014
OpenAlexW2902285227

What OpenQuestion 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 OpenQuestion graph.