Evidence map›Paper›PMID 35008216›Full record

ReviewCancers2021

Targeting the Intrinsic Apoptosis Pathway: A Window of Opportunity for Prostate Cancer.

Daniel Westaby, Juan M Jimenez-Vacas, Ana Padilha, Andreas Varkaris, Steven P Balk, Johann S de Bono, Adam Sharp

Abstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Review
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  17. Advancements in programmed cell death research in antitumor therapy: a comprehensive overview.Apoptosis : an international journal on programmed cell death · 2025
    Review
  18. Article
  19. Review
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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

7 authors.

Daniel WestabyDivision of Clinical Studies, The Institute of Cancer Research, London SM2 5NG, UK.ORCID 0000-0003-2996-4359
Juan M Jimenez-VacasDivision of Clinical Studies, The Institute of Cancer Research, London SM2 5NG, UK.
Ana PadilhaDivision of Clinical Studies, The Institute of Cancer Research, London SM2 5NG, UK.
Andreas VarkarisHematology-Oncology Division, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Steven P BalkHematology-Oncology Division, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Johann S de BonoDivision of Clinical Studies, The Institute of Cancer Research, London SM2 5NG, UK.
Adam SharpDivision of Clinical Studies, The Institute of Cancer Research, London SM2 5NG, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite major improvements in the management of advanced prostate cancer over the last 20 years, the disease remains invariably fatal, and new effective therapies are required. The development of novel hormonal agents and taxane chemotherapy has improved outcomes, although primary and acquired resistance remains problematic. Inducing cancer cell death via apoptosis has long been an attractive goal in the treatment of cancer. Apoptosis, a form of regulated cell death, is a highly controlled process, split into two main pathways (intrinsic and extrinsic), and is stimulated by a multitude of factors, including cellular and genotoxic stress. Numerous therapeutic strategies targeting the intrinsic apoptosis pathway are in clinical development, and BH3 mimetics have shown promising efficacy for hematological malignancies. Utilizing these agents for solid malignancies has proved more challenging, though efforts are ongoing. Molecular characterization and the development of predictive biomarkers is likely to be critical for patient selection, by identifying tumors with a vulnerability in the intrinsic apoptosis pathway. This review provides an up-to-date overview of cell death and apoptosis, specifically focusing on the intrinsic pathway. It summarizes the latest approaches for targeting the intrinsic apoptosis pathway with BH3 mimetics and discusses how these strategies may be leveraged to treat prostate cancer.

Indexed as

apoptosisBH3 mimeticscell deathprostate cancer

Identifiers

PMID35008216
PMCPMC8750516

What Socratic 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 Socratic graph.