Evidence map›Paper›PMID 32972043›Full record

ArticleCancer research and treatment2021

TM4SF4 and LRRK2 Are Potential Therapeutic Targets in Lung and Breast Cancers through Outlier Analysis.

Kyungsoo Jung, Joon-Seok Choi, Beom-Mo Koo, Yu Jin Kim, Ji-Young Song, Minjung Sung, Eun Sol Chang, Ka-Won Noh, Sungbin An, Mi-Sook Lee and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Cancer research and treatment, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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

16 authors at 7 institutions in 2 countries.

Kyungsoo JungDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Joon-Seok ChoiCollege of Pharmacy, Daegu Catholic University, Daegu, Korea.
Beom-Mo KooDepartment of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Korea.
Yu Jin KimLaboratory of Cancer Genomics and Molecular Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Ji-Young SongLaboratory of Cancer Genomics and Molecular Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Minjung SungLaboratory of Cancer Genomics and Molecular Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Eun Sol ChangLaboratory of Cancer Genomics and Molecular Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Ka-Won NohDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Sungbin AnDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Mi-Sook LeeDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Kyoung SongCollege of Pharmacy, Duksung Women's University, Seoul, Korea.
Hannah LeeInterdisciplinary Program in Bioinformatics, College of Natural Science, Seoul National University, Seoul, Korea.
Ryong Nam KimBio-MAX/N-BIO, Seoul National University, Seoul, Korea.
Young Kee ShinDepartment of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Korea.
Doo-Yi OhDepartment of Otorhinolaryngology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
Yoon-La ChoiDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Sungkyunkwan University · KRSamsung Medical Center · KRSeoul National University · KRCancer Research Institute · USDaegu Catholic University · KRDuksung Women's University · KRSeoul National University Bundang Hospital · KR

Funding

National Research Foundation of Korea 2015H1A2A1034732National Research Foundation of Korea 2016R1A5A2945889National Research Foundation of Korea 2019R1A2B5B02069979
6 · The paper itself

Abstract

purposeTo find biomarkers for disease, there have been constant attempts to investigate the genes that differ from those in the disease groups. However, the values that lie outside the overall pattern of a distribution, the outliers, are frequently excluded in traditional analytical methods as they are considered to be 'some sort of problem.' Such outliers may have a biologic role in the disease group. Thus, this study explored new biomarker using outlier analysis, and verified the suitability of therapeutic potential of two genes (TM4SF4 and LRRK2). MATERIALS AND

methodsModified Tukey's fences outlier analysis was carried out to identify new biomarkers using the public gene expression datasets. And we verified the presence of the selected biomarkers in other clinical samples via customized gene expression panels and tissue microarrays. Moreover, a siRNA-based knockdown test was performed to evaluate the impact of the biomarkers on oncogenic phenotypes.

resultsTM4SF4 in lung cancer and LRRK2 in breast cancer were chosen as candidates among the genes derived from the analysis. TM4SF4 and LRRK2 were overexpressed in the small number of samples with lung cancer (4.20%) and breast cancer (2.42%), respectively. Knockdown of TM4SF4 and LRRK2 suppressed the growth of lung and breast cancer cell lines. The LRRK2 overexpressing cell lines were more sensitive to LRRK2-IN-1 than the LRRK2 under-expressing cell lines.

conclusionOur modified outlier-based analysis method has proved to rescue biomarkers previously missed or unnoticed by traditional analysis showing TM4SF4 and LRRK2 are novel target candidates for lung and breast cancer, respectively.

Indexed as

Breast NeoplasmsFemaleHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2Lung NeoplasmsMembrane GlycoproteinsMolecular Targeted TherapyLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanMembrane GlycoproteinsTM4SF4 protein, humanLRRK2Molecular targeted therapyTM4SF4

Identifiers

PMID32972043
PMCPMC7812009
OpenAlexW3089015732

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.