Evidence map›Paper›PMID 32931887›Full record

ArticleCancer letters2021

Negative cross talk between LIMK2 and PTEN promotes castration resistant prostate cancer pathogenesis in cells and in vivo.

Kumar Nikhil, Mohini Kamra, Asif Raza, Kavita Shah

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cancer letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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  5. Regulation and signaling of the LIM domain kinases.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Kumar NikhilDepartment of Chemistry and Purdue University Center for Cancer Research 560 Oval Drive, West Lafayette, IN, 47907, USA.
Mohini KamraDepartment of Chemistry and Purdue University Center for Cancer Research 560 Oval Drive, West Lafayette, IN, 47907, USA.
Asif RazaDepartment of Chemistry and Purdue University Center for Cancer Research 560 Oval Drive, West Lafayette, IN, 47907, USA.
Kavita ShahDepartment of Chemistry and Purdue University Center for Cancer Research 560 Oval Drive, West Lafayette, IN, 47907, USA. Electronic address: shah23@purdue.edu.
Purdue University West Lafayette · US

Funding

Targeting Drug-Resistant Castration Resistant Prostate Cancer via LIMK2R01CA237660 · NCI · PURDUE UNIVERSITY · PI RATLIFF, TIMOTHY L. · 2020 to 2024
$1.2M
NCI NIH HHS R01 CA237660
6 · The paper itself

Abstract

Androgen deprivation therapy (ADT) and androgen receptor (AR) signaling inhibitors are front-line treatments for highly aggressive prostate cancer. However, prolonged inhibition of AR triggers a compensatory activation of PI3K pathway, most often due to the genomic loss of tumor suppressor PTEN, driving progression to the castration-resistant prostate cancer (CRPC) stage, which has very poor prognosis. We uncovered a novel mechanism of PTEN downregulation triggered by LIMK2, which contributes significantly to CRPC pathogenesis. LIMK2 is a CRPC-specific target. Its depletion fully reverses tumorigenesis in vivo. LIMK2 phosphorylates PTEN at five sites, degrading and inhibiting its activity, thereby driving highly aggressive oncogenic phenotypes in cells and in vivo. PTEN also degrades LIMK2 in a feedback loop, which was confirmed in prostates from PTEN

Indexed as

AnimalsCarcinogenesisCell LineCell Line, TumorDisease ProgressionDown-RegulationHEK293 CellsHumansHypoxiaLim KinasesMaleMiceMice, NudePC-3 CellsPhosphatidylinositol 3-KinasesProstateLIMK2 protein, humanLim KinasesPhosphatidylinositol 3-KinasesPTEN PhosphohydrolasePTEN protein, humanReceptors, AndrogenAKTCastration resistant prostate cancerEMTLIMK2PI3KPTEN

Identifiers

PMID32931887
PMCPMC8633979
OpenAlexW3086196032

What OpenQuestion holds

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LicenceTDM
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.