Evidence map›Paper›PMID 35205210›Full record

ReviewGenes2022

Splicing Variants, Protein-Protein Interactions, and Drug Targeting in Hutchinson-Gilford Progeria Syndrome and Small Cell Lung Cancer.

Bae-Hoon Kim, Tae-Gyun Woo, So-Mi Kang, Soyoung Park, Bum-Joon Park

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2022. 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
0.6field-weighted citation impact, top 37% 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, 7 citations in OpenAlex.

  1. Intermediate filaments and their associated molecules.Journal of biomedical research · 2025
    Article
  2. Article
  3. Review
  4. 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

5 authors at 1 institution in 1 country.

Bae-Hoon KimRare Disease R&D Center, PRG S&T Co., Ltd., Busan 46241, Korea.
Tae-Gyun WooRare Disease R&D Center, PRG S&T Co., Ltd., Busan 46241, Korea.
So-Mi KangDepartment of Molecular Biology, College of Natural Science, Pusan National University, Busan 46274, Korea.
Soyoung ParkDepartment of Molecular Biology, College of Natural Science, Pusan National University, Busan 46274, Korea.
Bum-Joon ParkRare Disease R&D Center, PRG S&T Co., Ltd., Busan 46241, Korea.ORCID 0000-0002-6037-7219
Pusan National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative splicing (AS) is a biological operation that enables a messenger RNA to encode protein variants (isoforms) that give one gene several functions or properties. This process provides one of the major sources of use for understanding the proteomic diversity of multicellular organisms. In combination with post-translational modifications, it contributes to generating a variety of protein-protein interactions (PPIs) that are essential to cellular homeostasis or proteostasis. However, cells exposed to many kinds of stresses (aging, genetic changes, carcinogens, etc.) sometimes derive cancer or disease onset from aberrant PPIs caused by DNA mutations. In this review, we summarize how splicing variants may form a neomorphic protein complex and cause diseases such as Hutchinson-Gilford progeria syndrome (HGPS) and small cell lung cancer (SCLC), and we discuss how protein-protein interfaces obtained from the variants may represent efficient therapeutic target sites to treat HGPS and SCLC.

Indexed as

Lung NeoplasmsProgeriaSmall Cell Lung CarcinomaDrug Delivery SystemsHumansLamin Type AProteomicsLamin Type Aalternative splicing (AS)DX2Hutchinson-Gilford progeria syndrome (HGPS)Progerinprotein-protein interactions (PPIs)small cell lung cancer (SCLC)

Identifiers

PMID35205210
PMCPMC8871687
OpenAlexW4206700631

What OpenQuestion 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 OpenQuestion graph.