Evidence map›Paper›PMID 41596257›Full record

ArticleInternational journal of molecular sciences2026

Approach to Design of Potent RNA Interference-Based Preparations Against Hepatocellular Carcinoma-Related Genes.

Petr V Chernov, Vladimir N Ivanov, Nikolai A Dmitriev, Artem E Gusev, Valeriia I Kovchina, Ivan S Gongadze, Alexander V Kholstov, Maiia V Popova, Dmitry A Kudlay, Daria S Kryuchko and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Petr V ChernovNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0009-0005-0642-8723
Vladimir N IvanovNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0009-0002-8492-2979
Nikolai A DmitrievNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0009-0002-8381-8512
Artem E GusevNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0009-0002-5810-098X
Valeriia I KovchinaNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0000-0003-3134-5776
Ivan S GongadzeNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0009-0009-3253-369X
Alexander V KholstovNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0009-0004-0178-609X
Maiia V PopovaNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0000-0002-3671-780X
Dmitry A KudlayNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0000-0003-1878-4467
Daria S KryuchkoFederal Medical-Biological Agency, 123182 Moscow, Russia.ORCID 0000-0001-9047-6050
Ilya A KofiadiNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0000-0001-9280-8282
Musa R KhaitovNRC Institute of Immunology FMBA of Russia, 115522 Moscow, Russia.ORCID 0000-0003-4961-9640

Funding

Russian Science Foundation 25-25-00281
6 · The paper itself

Abstract

Every year, the scientific community continues to drive advances in healthcare, opening up new perspectives in the treatment and management of various diseases. Despite vast strides being made in the quality of life and longevity, we still face an equally significant growth in the burden of oncological pathologies. Although current trends lean towards preventive and personalized medicine, numerous hurdles remain to be cleared to develop robust strategies in the field of oncology. Among all types of tumors, one of the prominent positions is occupied by hepatocellular carcinoma (HCC), which is one of the most widespread primary cancers with a high mortality rate. Conventional approaches to HCC therapy, such as surgery or chemotherapy, rarely provide steady performance due to the highly polymorphous nature of the cancerous process. In this study, we suggest an alternative methodological framework for designing potent siRNAs targeting genes implicated in hepatocellular carcinoma, implementing RNA interference mediated by synthetic small interfering RNAs (siRNAs) against mRNAs of

Indexed as

Carcinoma, HepatocellularCD47 AntigenLiver NeoplasmsRNA InterferenceRNA, Small InterferingAlgorithmsCell Line, TumorGene Expression Regulation, NeoplasticHumansIntegrin beta1CD47 AntigenIntegrin beta1Itgb1 protein, humanRNA, Small InterferingCD47HCChepatocellular carcinomain silico drug designITGB1RNAisiRNA

Identifiers

PMID41596257
PMCPMC12841486

What Socratic 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 Socratic graph.