Evidence map›Paper›PMID 38894916›Full record

ArticleACS medicinal chemistry letters2024

Novel Approaches for Upregulation of Tumor Suppressor Proteins: Pioneering Strategies and Integrative Potentials.

Robert B Kargbo

Abstract readEditorial
In one paragraph

Article in ACS medicinal chemistry letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Robert B KargboUsona Institute, Fitchburg, Wisconsin 53711-5300, United States.ORCID https://orcid.org/0000-0002-5539-6343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cancer therapy, the modulation of tumor suppressor proteins represents a critical frontier in developing innovative treatments. A promising direction in this field is the strategic upregulation of tumor suppressor proteins, a paradigm illustrated by the development of compounds designed to enhance the activity of the p53 protein. This protein, often called the "guardian of the genome", is crucial in preventing cancer development by inducing cell cycle arrest, apoptosis, and senescence in response to DNA damage and oncogenic stress. However, p53 function is compromised in many cancers, leading to unchecked cell proliferation and tumor progression. Addressing this challenge, a novel approach focuses on manipulating the p53/MDM2 signaling pathway to restore p53's tumor-suppressive functions.

Identifiers

PMID38894916
PMCPMC11181502

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.