Evidence map›Paper›PMID 34363546›Full record

ArticleMedical oncology (Northwood, London, England)2021

Molecular analysis of cell survival and death pathways in the proteasome inhibitor bortezomib-resistant PC3 prostate cancer cell line.

Ertan Kanbur, Ahmet Tarık Baykal, Azmi Yerlikaya

Abstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
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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

3 authors at 3 institutions in 1 country.

Ertan KanburDepartment of Immunology, Faculty of Medicine, Bursa Uludağ University, Bursa, Turkey.
Ahmet Tarık BaykalDepartment of Medical Biochemistry, Faculty of Medicine, Acıbadem Mehmet Ali Aydınlar University, Istanbul, Turkey.
Azmi YerlikayaDepartment of Medical Biology, Faculty of Medicine, Kutahya Health Sciences University, Kutahya, Turkey. azmi.yerlikaya@ksbu.edu.tr.ORCID http://orcid.org/0000-0002-0678-0701
Bursa Uludağ Üni̇versi̇tesi̇ · TRDumlupinar University · TRKent Hastanesi · TR

Funding

türkiye bilimsel ve teknolojik araştirma kurumu 119Z145
6 · The paper itself

Abstract

The ubiquitin-proteasome pathway is an important protein quality control system involved in intracellular homeostasis. To achieve intracellular homeostasis, proteins that are misfolded as a result of translational errors or genetic mutations must be eliminated by the ubiquitin-proteasome pathway. In our previous publications, we determined that 4T1 breast and B16F10 melanoma cancer cells have differential levels of resistance to proteasome inhibitors. Again, in the previous studies, we reported that 4T1 cell cultures, despite being p53-mutant, underwent apoptosis as a result of bortezomib treatment. The first goal of this study was to verify the resistance levels of parental and resistant PC3 prostate cancer cells to bortezomib using WST-1 test. As a result of treatment with different bortezomib concentrations for 48 h, the IC

Indexed as

ApoptosisAutophagyAntineoplastic AgentsBiomarkers, TumorBortezomibCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticHumansMalePC-3 CellsPhosphorylationProstatic NeoplasmsAntineoplastic AgentsBiomarkers, TumorBortezomibBortezomibCancerCDK2ERKLC3MELKProstate

Identifiers

PMID34363546
OpenAlexW3191097563

What OpenQuestion holds

Textmetadata
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.