Evidence map›Paper›PMID 33734457›Full record

ArticleThe Prostate2021

Periprostatic adipose tissue promotes prostate cancer resistance to docetaxel by paracrine IGF-1 upregulation of TUBB2B beta-tubulin isoform.

Antonietta Liotti, Evelina La Civita, Michele Cennamo, Felice Crocetto, Matteo Ferro, Elia Guadagno, Luigi Insabato, Ciro Imbimbo, Alessandro Palmieri, Vincenzo Mirone and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
9.2field-weighted citation impact, top 1% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

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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

14 authors at 3 institutions in 2 countries.

Antonietta LiottiDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Evelina La CivitaDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Michele CennamoDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Felice CrocettoDepartment of Neurosciences, University of Naples Federico II, Naples, Italy.
Matteo FerroDepartment of Urology, European Institute of Oncology, IRCCS, Milan, Italy.
Elia GuadagnoDepartment of Advanced Biomedical Sciences, Anatomic Pathology Unit, School of Medicine, University of Naples Federico II, Naples, Italy.
Luigi InsabatoDepartment of Advanced Biomedical Sciences, Anatomic Pathology Unit, School of Medicine, University of Naples Federico II, Naples, Italy.
Ciro ImbimboDepartment of Neurosciences, University of Naples Federico II, Naples, Italy.
Alessandro PalmieriDepartment of Neurosciences, University of Naples Federico II, Naples, Italy.
Vincenzo MironeDepartment of Neurosciences, University of Naples Federico II, Naples, Italy.
Pasquale LiguoroDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Pietro FormisanoDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Francesco BeguinotDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Daniela TerraccianoDepartment of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.ORCID 0000-0003-4296-429X
University of Naples Federico II · ITFederico II University Hospital · ITEuropean Institute of Oncology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence supports the pivotal role played by periprostatic adipose tissue (PPAT) in prostate cancer (PCa) microenvironment. We investigated whether PPAT can affect response to Docetaxel (DCTX) and the mechanisms associated. Conditioned medium was collected from the in vitro differentiated adipocytes isolated from PPAT which was isolated from PCa patients, during radical prostatectomy. Drug efficacy was studied by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide citotoxicity assay. Culture with CM of human PPAT (AdipoCM) promotes DCTX resistance in two different human prostate cancer cell lines (DU145 and PC3) and upregulated the expression of BCL-xL, BCL-2, and TUBB2B. AG1024, a well-known IGF-1 receptor inhibitor, counteracts the decreased response to DCTX observed in presence of AdipoCM and decreased TUBB2B expression, suggesting that a paracrine secretion of IGF-1 by PPAT affect DCTX response of PCa cell. Collectively, our study showed that factors secreted by PPAT elicits DCTX resistance through antiapoptotic proteins and TUBB2B upregulation in androgen independent PCa cell lines. These findings reveal the potential of novel therapeutic strategies targeting adipocyte-released factors and IGF-1 axis to overcome DCTX resistance in patients with PCa.

Indexed as

Gene Expression Regulation, NeoplasticAdipose TissueAntineoplastic AgentsCell Line, TumorDocetaxelDrug Resistance, NeoplasmHumansInsulin-Like Growth Factor IMaleParacrine CommunicationProstatic NeoplasmsTubulinUp-RegulationAntineoplastic AgentsDocetaxelInsulin-Like Growth Factor ITUBB2B protein, humanTubulinadipocytesdocetaxeldrug resistanceperiprostatic adipose tissueprostate cancer

Identifiers

PMID33734457
PMCPMC8251776
OpenAlexW3138908545

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.