Evidence map›Paper›PMID 35657000›Full record

ArticleJournal of breast cancer2022

Mutational Analysis of Triple-Negative Breast Cancer Using Targeted Kinome Sequencing.

Tae-Kyung Yoo, Woo Seung Lee, Jisun Kim, Min Kyoon Kim, In-Ae Park, Ju Han Kim, Wonshik Han

Open access · goldAbstract read
In one paragraph

Article in Journal of breast cancer, 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
0.3field-weighted citation impact, top 52% 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, 3 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Oncology letters · 2025
    Article
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

7 authors at 4 institutions in 1 country.

Tae-Kyung Yoo *Department of Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-5790-353X
Woo Seung Lee *Division of Biomedical Informatics, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-7848-0639
Jisun KimDivision of Breast Surgery, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4884-6107
Min Kyoon KimDepartment of Surgery, Chung-Ang University Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-1848-7801
In-Ae ParkDepartment of Pathology, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8759-4934
Ju Han KimDivision of Biomedical Informatics, Seoul National University College of Medicine, Seoul, Korea. juhan@snu.ac.kr.ORCID https://orcid.org/0000-0003-1522-9038
Wonshik HanDepartment of Surgery, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-7310-0764
Seoul National University · KRUlsan College · KRChung-Ang University Hospital · KRThe Catholic University of Korea Seoul St. Mary's Hospital · KR

Funding

SK Telecom
6 · The paper itself

Abstract

purposeTriple-negative breast cancer (TNBC) does not have defined therapeutic targets and is currently treated with chemotherapy only. Kinase dysregulation triggers cancer cell proliferation and metastasis and is a crucial therapeutic target for cancer. In this study, targeted kinome sequencing of TNBC tumors was performed to assess the association between kinome gene alterations and disease outcomes in TNBC.

methodsA kinome gene panel consisting of 612 genes was used for the targeted sequencing of 166 TNBC samples and matched normal tissues. Analyses of the significantly mutated genes were performed. Genomic differences between Asian and non-Asian patients with TNBC were evaluated using two Asian TNBC datasets (from Seoul National University Hospital [SNUH] and Fudan University Shanghai Cancer Center [FUSCC]) and three non-Asian TNBC datasets (The Cancer Genome Atlas [TCGA], METABRIC, and Gustave Roussy). The prognostic value of kinome gene mutations was evaluated using tumor mutational burden (TMB) and oncogenic pathway analyses. Mutational profiles from the TCGA were used for validation.

resultsThe significantly mutated genes included

conclusionComprehensive analyses of kinome gene alterations in TNBC revealed genomic alterations that offer therapeutic targets and should help identify high-risk patients more precisely in future studies.

Indexed as

MutationProtein KinasesSurvivalTriple Negative Breast Neoplasms

Identifiers

PMID35657000
PMCPMC9250872
OpenAlexW4226208711

What OpenQuestion holds

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LicenceCC BY-NC
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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.