Evidence map›Paper›PMID 31083670›Full record

ArticlePloS one2019

Knockdown of PTOV1 and PIN1 exhibit common phenotypic anti-cancer effects in MDA-MB-231 cells.

Shibendra Kumar Lal Karna, Faiz Ahmad, Bilal Ahmad Lone, Yuba Raj Pokharel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Prognostic value of peptidyl-prolyl cis-trans isomerase 1 (PIN1) in human malignant tumors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
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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

4 authors at 1 institution in 1 country.

Shibendra Kumar Lal KarnaCancer Biology Laboratory, Faculty of Life Science & Biotechnology, South Asian University, Akbar Bhawan, Chankyapuri, New Delhi, India.
Faiz AhmadCancer Biology Laboratory, Faculty of Life Science & Biotechnology, South Asian University, Akbar Bhawan, Chankyapuri, New Delhi, India.
Bilal Ahmad LoneCancer Biology Laboratory, Faculty of Life Science & Biotechnology, South Asian University, Akbar Bhawan, Chankyapuri, New Delhi, India.
Yuba Raj PokharelCancer Biology Laboratory, Faculty of Life Science & Biotechnology, South Asian University, Akbar Bhawan, Chankyapuri, New Delhi, India.ORCID 0000-0002-1202-5120
South Asian University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarlier, we have identified PTOV1 as a novel interactome of PIN1 in PC-3 cells. This study aims to explore the functional similarity and the common role of both genes in breast cancer cell proliferation.

methodsCTG, crystal violet assay, clonogenic assay, wound healing assay, cell cycle analysis, Hoechst staining and ROS measurement were performed to assess cell viability, colony forming potential, cell cycle arrest, nuclear condensation and ROS production after knocking down of PTOV1 and PIN1 by siRNAs in MDA-MB-231 and MCF-7 cells. CO-IP, qPCR and western blot were performedto study interaction, transcriptional and translational regulation of both genes.

resultsKnockdown of PTOV1 and PIN1 inhibited the cell proliferation, colony formation, migration, cell cycle, and induced nuclear condensation as well as ROS production. Interaction of PTOV1 and PIN1 was validated by Co-IP in MDA-MB-231 cells. Genes involved in cell proliferation, migration, cell cycle, and apoptosis were regulated by PIN1 and PTOV1. PTOV1 knockdown inhibited Bcl-2, Bcl-xL and inducedBAX, LC3 and Beclin-1expression. Overexpression of PIN1 increased the expression of PTOV1. Knockdown of both genes inhibited the expression of cyclin D1, c-Myc, and β-catenin.

conclusionsPTOV1 and PIN1 interact and exert oncogenic role in MDA-MB-231 cells by sharing the similar expression profile at transcriptional and translational level which can be a promising hub for therapeutic target.

Indexed as

Gene Knockdown TechniquesGenetic Predisposition to DiseasePhenotypeAdaptor Proteins, Signal TransducingBiomarkers, TumorBreast NeoplasmsCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationCell SurvivalFemaleGene Expression Regulation, NeoplasticHumansModels, BiologicalNeoplasm ProteinsAdaptor Proteins, Signal TransducingBiomarkers, TumorNeoplasm ProteinsNIMA-Interacting Peptidylprolyl IsomerasePIN1 protein, humanPTOV1 protein, humanReactive Oxygen SpeciesRNA, Small Interfering

Identifiers

PMID31083670
PMCPMC6513092
OpenAlexW2949167470

What OpenQuestion holds

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LicenceCC BY
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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.