Evidence map›Paper›PMID 36322312›Full record

ArticleBulletin of experimental biology and medicine2022

Suppression of the Antioxidant System and PI3K/Akt/mTOR Signaling Pathway in Cisplatin-Resistant Cancer Cells by Quercetin.

A A Sh Hasan, E V Kalinina, V V Tatarskiy, Yu L Volodina, А S Petrova, M D Novichkova, D D Zhdanov, A A Shtil

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In one paragraph

Article in Bulletin of experimental biology and medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  8. Natural Compounds for Preventing Age-Related Diseases and Cancers.International journal of molecular sciences · 2024
    Review
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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

8 authors at 2 institutions in 1 country.

A A Sh HasanT. T. Berezov Department of Biochemistry, Peoples' Friendship University of Russia (RUDN University), Moscow, Russia.
E V KalininaT. T. Berezov Department of Biochemistry, Peoples' Friendship University of Russia (RUDN University), Moscow, Russia. elena.v.kalinina@gmail.com.
V V TatarskiyLaboratory of Tumor Cell Death, N. N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russia.
Yu L VolodinaLaboratory of Tumor Cell Death, N. N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russia.
А S PetrovaT. T. Berezov Department of Biochemistry, Peoples' Friendship University of Russia (RUDN University), Moscow, Russia.
M D NovichkovaT. T. Berezov Department of Biochemistry, Peoples' Friendship University of Russia (RUDN University), Moscow, Russia.
D D ZhdanovT. T. Berezov Department of Biochemistry, Peoples' Friendship University of Russia (RUDN University), Moscow, Russia.
A A ShtilLaboratory of Tumor Cell Death, N. N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russia.
Peoples' Friendship University of Russia · RUMinistry of Health of the Russian Federation · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We studied the effect of quercetin on ovarian adenocarcinoma SKOV-3 cell line and isogenic subline SKOV-3/CDDP resistant to the anticancer drug cisplatin. It was found that in resistant cells, quercetin in a concentration of 100 μM that causes a decrease in the cell viability suppressed the expression of genes encoding the key antioxidant enzymes (SOD2, CAT, GPX1, and HO-1), transcription factor Nrf2, and kinases of the PI3K/Akt/mTOR signaling pathway. In parental cells, quercetin, on the contrary, increased the expression of these genes. The results confirm the redox-dependent regulation induced by quercetin and its opposite nature in cisplatin-sensitive and cisplatin-resistant cancer cells.

Indexed as

CisplatinOvarian NeoplasmsAntioxidantsApoptosisCell Line, TumorDrug Resistance, NeoplasmFemaleHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuercetinSignal TransductionTOR Serine-Threonine KinasesAntioxidantsCisplatinMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuercetinTOR Serine-Threonine Kinasesdrug resistance of tumor cellsgene expressionPI3K-AkT-mTOR signaling pathwayquercetin

Identifiers

PMID36322312
OpenAlexW4307971721

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.