Evidence map›Paper›PMID 39537875›Full record

ArticleOncogene2025

Unveiling RACK1: a key regulator of the PI3K/AKT pathway in prostate cancer development.

Cancan Lyu, Prasanna Kuma Vaddi, Said Elshafae, Anirudh Pradeep, Deqin Ma, Songhai Chen

Abstract read
In one paragraph

Article in Oncogene, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  9. 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

6 authors.

Cancan LyuDepartments of Neuroscience and Pharmacology, University of Iowa, Iowa City, USA.
Prasanna Kuma VaddiDepartments of Neuroscience and Pharmacology, University of Iowa, Iowa City, USA.
Said ElshafaeDepartments of Neuroscience and Pharmacology, University of Iowa, Iowa City, USA.
Anirudh PradeepDepartments of Neuroscience and Pharmacology, University of Iowa, Iowa City, USA.
Deqin MaDepartments of Phathology, University of Iowa, Iowa City, USA.
Songhai ChenDepartments of Neuroscience and Pharmacology, University of Iowa, Iowa City, USA. songhai-chen@uiowa.edu.ORCID 0000-0001-7316-7125

Funding

Role of Gi/o-GPCR signaling in breast cancer progressionR01CA207889 · NCI · UNIVERSITY OF IOWA · PI CHEN, SONGHAI, WEIGEL, RONALD J · 2017 to 2021
$2.3M
Role of the CTLH E3 ubiquitin ligase in breast cancer progressionR01CA282699 · NCI · UNIVERSITY OF IOWA · PI Songhai Chen, RONALD J WEIGEL · 2024 to 2026
$1.5M
IVIS Biolumenscence and Fluorescence Live Animal ImagingS10OD026835 · OD · UNIVERSITY OF IOWA · PI RICE, KEVIN G · 2019 to 2019
$257k
NCI NIH HHS R01 CA207889NCI NIH HHS R01 CA282699U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1S10OD026835-01
6 · The paper itself

Abstract

The dysregulated PI3K/AKT pathway is pivotal in the onset and progression of various cancers, including prostate cancer. However, targeting this pathway directly poses challenges due to compensatory upregulation of alternative oncogenic pathways. This study focuses on the novel regulatory activity of the Receptor for Activated Protein Kinase (RACK1), a scaffolding/adaptor protein, in governing the PI3K/AKT pathway within prostate cancer. Through a genetic mouse model, our research unveils RACK1's pivotal role in orchestrating AKT activation and the genesis of prostate cancer. RACK1 deficiency hampers AKT activation, effectively impeding prostate tumor formation induced by PTEN and p53 deficiency. Mechanistically, RACK1 facilitates AKT membrane translocation and fosters its interaction with mTORC2, thereby promoting AKT activation and subsequent tumor cell proliferation and tumor formation. Notably, inhibiting AKT activation via RACK1 deficiency does not trigger feedback upregulation of HER3 and androgen receptor (AR) expression and activation, distinguishing it from direct PI3K or AKT targeting. These findings position RACK1 as a critical regulator of the PI3K/AKT pathway and a promising target for curtailing prostate cancer development arising from pathway aberrations.

Indexed as

Neoplasm ProteinsPhosphatidylinositol 3-KinasesProstatic NeoplasmsProto-Oncogene Proteins c-aktReceptors for Activated C KinaseAnimalsCell ProliferationGene Expression Regulation, NeoplasticHumansMaleMicePTEN PhosphohydrolaseReceptors, AndrogenSignal TransductionNeoplasm ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseRACK1 protein, humanRACK1 protein, mouseReceptors, AndrogenReceptors for Activated C Kinase

Identifiers

PMID39537875
PMCPMC13006131

What OpenQuestion holds

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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.