Evidence map›Paper›PMID 35465350›Full record

ArticleJournal of immunology research2022

Combination Blockade of the IL6R/STAT-3 Axis with TIGIT and Its Impact on the Functional Activity of NK Cells against Prostate Cancer Cells.

S González-Ochoa, M C Tellez-Bañuelos, A S Méndez-Clemente, A Bravo-Cuellar, G Hernández Flores, L A Palafox-Mariscal, J Haramati, E J Pedraza-Brindis, K Sánchez-Reyes, P C Ortiz-Lazareno

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-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

12 citing papers in PubMed, 15 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

10 authors at 3 institutions in 1 country.

S González-OchoaInstituto Mexicano del Seguro Social (IMSS), Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Guadalajara, 44340, Jalisco, Mexico.
M C Tellez-BañuelosUniversidad de Guadalajara, Centro Universitario de Ciencias de la Salud (CUCS), Programa de Doctorado en Ciencias Biomédicas Orientación Inmunología, Guadalajara, 44340, Jalisco, Mexico.ORCID https://orcid.org/0000-0002-9057-1397
A S Méndez-ClementeInstituto Mexicano del Seguro Social (IMSS), Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Guadalajara, 44340, Jalisco, Mexico.
A Bravo-CuellarInstituto Mexicano del Seguro Social (IMSS), Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Guadalajara, 44340, Jalisco, Mexico.
G Hernández FloresInstituto Mexicano del Seguro Social (IMSS), Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Guadalajara, 44340, Jalisco, Mexico.
L A Palafox-MariscalInstituto Mexicano del Seguro Social (IMSS), Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Guadalajara, 44340, Jalisco, Mexico.
J HaramatiUniversidad de Guadalajara, Centro Universitario de Ciencias de la Salud (CUCS), Programa de Doctorado en Ciencias Biomédicas Orientación Inmunología, Guadalajara, 44340, Jalisco, Mexico.
E J Pedraza-BrindisUniversidad de Guadalajara, Centro Universitario de Ciencias de la Salud (CUCS), HIV and Immunodeficiencies Research Institute, Clinical Medicine Department, Guadalajara, 44280, Jalisco, Mexico.
K Sánchez-ReyesUniversidad de Guadalajara, Centro Universitario de Ciencias de la Salud (CUCS), HIV and Immunodeficiencies Research Institute, Clinical Medicine Department, Guadalajara, 44280, Jalisco, Mexico.
P C Ortiz-LazarenoInstituto Mexicano del Seguro Social (IMSS), Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Guadalajara, 44340, Jalisco, Mexico.ORCID https://orcid.org/0000-0001-9045-7052
Mexican Social Security Institute · MXUniversidad de Guadalajara · MXUniversidad Autónoma de Guadalajara · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methods: We analyzed the secretion of cytokines, chemokines, and growth factors in 22Rv1, LNCaP, and DU145 cells. In these cells, we also evaluated the expression of NK ligands, IL6R, STAT-3, and phosporylated STAT-3. In NK-92 cells, we evaluated the effects of Stattic (Stt) and tocilizumab (Tcz) on NK receptors. In addition, we assessed if the disruption of the IL6R/STAT-3 pathway and blockade of TIGIT potentiated the cytotoxicity of NK-92 cells versus DU145 cells. Results: DU145 abundantly secretes M-CSF, VEGF, IL-6, CXCL8, and TGF- Conclusions: Our results reveal that the combined use of inhibitors directed against the IL6R/STAT-3 axis and TIGIT enhances the functional activity of NK cells against castration-resistant prostate cancer cells.

Indexed as

Killer Cells, NaturalProstatic NeoplasmsHumansMaleProstateReceptors, ImmunologicReceptors, Interleukin-6IL6R protein, humanReceptors, ImmunologicReceptors, Interleukin-6TIGIT protein, human

Identifiers

PMID35465350
PMCPMC9020142
OpenAlexW4223544043

What OpenQuestion 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 OpenQuestion graph.