Evidence map›Paper›PMID 36318360›Full record

ArticleJournal of microbiology (Seoul, Korea)2022

Inhibition of KIF20A suppresses the replication of influenza A virus by inhibiting viral entry.

Hoyeon Jeon, Younghyun Lim, In-Gu Lee, Dong-In Kim, Keun Pil Kim, So-Hee Hong, Jeongkyu Kim, Youn-Sang Jung, Young-Jin Seo

Abstract read
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In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Deciphering European Sea Bass (International journal of molecular sciences · 2025
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  3. 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

9 authors at 2 institutions in 1 country.

Hoyeon JeonDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea.
Younghyun LimDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea.
In-Gu LeeDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea.
Dong-In KimDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea.
Keun Pil KimDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea.
So-Hee HongDepartment of Microbiology, College of Medicine, Ewha Womans University, Seoul, 07804, Republic of Korea.
Jeongkyu KimDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea. kimj@cau.ac.kr.
Youn-Sang JungDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea. younsang@cau.ac.kr.
Young-Jin SeoDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea. yjseo@cau.ac.kr.
Chung-Ang University · KREwha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The influenza A virus (IAV) has caused several pandemics, and therefore there are many ongoing efforts to identify novel antiviral therapeutic strategies including vaccines and antiviral drugs. However, influenza viruses continuously undergo antigenic drift and shift, resulting in the emergence of mutated viruses. In turn, this decreases the efficiency of existing vaccines and antiviral drugs to control IAV infection. Therefore, this study sought to identify alternative therapeutic strategies targeting host cell factors rather than viruses to avoid infection by mutated viruses. Particularly, we investigated the role of KIF20A that is one of kinesin superfamily proteins in the replication of IAV. The KIF20A increased viral protein levels in IAV-infected cells by regulating the initial entry stage during viral infection. Furthermore, the KIF20A inhibitor significantly suppressed viral replication, which protected mice from morbidity and mortality. Therefore, our findings demonstrated that KIF20A is highly involved in the viral replication process and viral propagation both in vitro and in vivo, and could thus be used as a target for the development of novel antiviral drugs.

Indexed as

Influenza A virusInfluenza, HumanAnimalsAntiviral AgentsHumansMiceVirus InternalizationVirus ReplicationAntiviral Agentsinfluenza A virusKIF20Apaprotrain

Identifiers

PMID36318360
OpenAlexW4308042277

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.