Evidence map›Paper›PMID 26716414›Full record

ArticleOncotarget2016

NTRK1 fusions for the therapeutic intervention of Korean patients with colon cancer.

Do Youn Park, Chan Choi, Eunji Shin, Jae Hyuk Lee, Chae Hwa Kwon, Hong-Jae Jo, Hyeong-Rok Kim, Hyun Sung Kim, Nahmgun Oh, Ji Shin Lee and 8 more

Open access · diamondAbstract readComparative Study
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Comprehensive analysis ofJournal of genetics · 2020
    Trial
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  4. Toward in vivo proof of binding ofEJNMMI research · 2022
    Article
  5. Detection ofDiagnostics (Basel, Switzerland) · 2022
    Article
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  10. Review
  11. Clinical and Molecular Characterization of Adult Glioblastomas in Southern Brazil.Journal of neuropathology and experimental neurology · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. 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

18 authors at 4 institutions in 1 country.

Do Youn ParkDepartment of Pathology, Pusan National University Hospital and Pusan National University School of Medicine, and BioMedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
Chan ChoiDepartment of Pathology, Chonnam National University Hwasun Hospital, Hwasun-gun, Jeollanam-do, Republic of Korea.
Eunji ShinLG Life Sciences Ltd., R&D Park, Daejeon, Republic of Korea.
Jae Hyuk LeeDepartment of Pathology, Chonnam National University Hwasun Hospital, Hwasun-gun, Jeollanam-do, Republic of Korea.
Chae Hwa KwonDepartment of Pathology, Pusan National University Hospital and Pusan National University School of Medicine, and BioMedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
Hong-Jae JoDepartment of Surgery, Pusan National University Hospital and Pusan National University School of Medicine, and BioMedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
Hyeong-Rok KimDepartment of Surgery, Chonnam National University Hwasun Hospital, Hwasun-gun, Jeollanam-do, Republic of Korea.
Hyun Sung KimDepartment of Surgery, Pusan National University Hospital and Pusan National University School of Medicine, and BioMedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
Nahmgun OhDepartment of Surgery, Pusan National University Hospital and Pusan National University School of Medicine, and BioMedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
Ji Shin LeeDepartment of Pathology, Chonnam National University Hwasun Hospital, Hwasun-gun, Jeollanam-do, Republic of Korea.
Ok Ku ParkLG Life Sciences Ltd., R&D Park, Daejeon, Republic of Korea.
Eok ParkLG Life Sciences Ltd., R&D Park, Daejeon, Republic of Korea.
Jonghoon ParkLG Life Sciences Ltd., R&D Park, Daejeon, Republic of Korea.
Jong-Yeon ShinGenomic Medicine Institute (GMI), Medical Research Center, Seoul National University, Seoul, Republic of Korea.
Jong-Il KimGenomic Medicine Institute (GMI), Medical Research Center, Seoul National University, Seoul, Republic of Korea.
Jeong-Sun SeoGenomic Medicine Institute (GMI), Medical Research Center, Seoul National University, Seoul, Republic of Korea.
Hee Dong ParkLG Life Sciences Ltd., R&D Park, Daejeon, Republic of Korea.
Joonghoon ParkLG Life Sciences Ltd., R&D Park, Daejeon, Republic of Korea.
Chonnam National University Hwasun Hospital · KRPusan National University Hospital · KRSeoul National University · KRMacrogen (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification and clinical validation of cancer driver genes are essential to accelerate the translational transition of cancer genomics, as well as to find clinically confident targets for the therapeutic intervention of cancers. Here we identified recurrent LMNA-NTRK1 and TPM3-NTRK1 fusions in Korean patients with colon cancer (3 out of 147, 2%) through next-generation RNA sequencing (RNA-seq). NTRK1 fusions were mutually exclusive oncogenic drivers of colon cancer that were accompanied with in vitro potential of colony formation and in vivo tumorigenicity comparable to KM12, a human colon cancer cell line harboring TPM3-NTRK1 fusion. NTRK1-encoded TrkA protein was prevalent in 11 out of 216 Korean (5.1%) and 28 out of 472 Chinese patients (5.9%) from independent cohorts, respectively. The expression level of TrkA was significantly correlated with NTRK1 fusion (p = 0.0192), which was verified by a fluorescence in situ hybridization (FISH). Korean patients with TrkA-positive colon cancer had a marginal but significant shorter overall survival time than TrkA-negative colon cancer [hazard ratio (HR) = 0.5346, 95% confidential interval (CI) = 0.2548-0.9722, p = 0.0411]. In addition, KM12 cell line was sensitive to selective TrkA inhibitors. These results demonstrate that NTRK1 fusion is granted as a clinically relevant target for therapeutic intervention of colon cancer.

Indexed as

AgedAnimalsCarbazolesCarcinogenesisCase-Control StudiesColonic NeoplasmsCrizotinibFemaleFollow-Up StudiesFuransGene FusionHigh-Throughput Nucleotide SequencingHumansImmunoenzyme TechniquesIn Situ Hybridization, FluorescenceLamin Type ACarbazolesCrizotinibFuransLamin Type AlestaurtinibLMNA protein, humanOncogene Proteins, FusionProtein Kinase InhibitorsPyrazolesPyridinesReceptor, trkARNA, MessengerTPM3 protein, humanTropomyosinKorean colon cancerNTRK1 fusionpredictive biomarkerRNA-seqtargeted therapy

Identifiers

PMID26716414
PMCPMC4885001
OpenAlexW2220937100

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Registered trials

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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.