Evidence map›Paper›PMID 29725014›Full record

ArticleNature communications2018

Clinical and genomic landscape of gastric cancer with a mesenchymal phenotype.

Sang Cheul Oh, Bo Hwa Sohn, Jae-Ho Cheong, Sang-Bae Kim, Jae Eun Lee, Ki Cheong Park, Sang Ho Lee, Jong-Lyul Park, Yun-Yong Park, Hyun-Sung Lee and 28 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 284 papers.

0numbers the graph read from it
0cells of the map it votes in
284citing papers in PubMed
22.9field-weighted citation impact, top 1% 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

284 citing papers in PubMed, 455 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Advances in the molecular subtyping of gastric cancer.World journal of surgical oncology · 2026
    Review
  10. Review
  11. Article
  12. Article
  13. Development and validation of a cuproptosis-related gene signature for predicting prognosis and drug sensitivity in gastric cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  14. Article
  15. Article
  16. Article
  17. Spatially defined danger zone shapes gastric cancer progression through CCDC80Apoptosis : an international journal on programmed cell death · 2026
    Article
  18. Article
  19. Article
  20. Article

224 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

38 authors at 8 institutions in 3 countries.

Sang Cheul OhDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Bo Hwa SohnDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Jae-Ho CheongDepartment of Surgery, Yonsei University College of Medicine, Seoul, 03722, Korea.
Sang-Bae KimDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Jae Eun LeeDepartment of Surgery, Yonsei University College of Medicine, Seoul, 03722, Korea.
Ki Cheong ParkDepartment of Surgery, Yonsei University College of Medicine, Seoul, 03722, Korea.
Sang Ho LeeDepartment of Surgery, Kosin University, College of Medicine, Busan, 49267, Korea.
Jong-Lyul ParkPersonalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Korea.
Yun-Yong ParkDepartment of Medicine, ASAN Institute for Life Sciences, ASAN Medical Center, University of Ulsan College of Medicine, Seoul, 05505, Korea.
Hyun-Sung LeeDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0001-8259-046X
Hee-Jin JangDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0001-7031-1398
Eun Sung ParkMedical Research Institute, College of Medicine, Inha University, Incheon, 22212, Korea.
Sang-Cheol KimDepartment of Biomedical Informatics, Center for Genome Science, National Institute of Health, Daejeon, 34141, Korea.
Jeonghoon HeoDepartment of Molecular Biology and Immunology, Kosin University, College of Medicine, Busan, 49267, Korea.
In-Sun ChuKorean Bioinformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Korea.
You-Jin JangDepartment of Surgery, Guro Hospital, College of Medicine, Korea University, Seoul, 08308, Korea.
Young-Jae MokDepartment of Surgery, Guro Hospital, College of Medicine, Korea University, Seoul, 08308, Korea.
WonKyung JungDepartment of Surgery, Guro Hospital, College of Medicine, Korea University, Seoul, 08308, Korea.
Baek-Hui KimDepartment of Pathology, Guro Hospital, College of Medicine, Korea University, Seoul, 08308, Korea.
Aeree KimDepartment of Pathology, Guro Hospital, College of Medicine, Korea University, Seoul, 08308, Korea.
Jae Yong ChoMedical Oncology, Yonsei University College of Medicine, Seoul, 03722, Korea.
Jae Yun LimMedical Oncology, Yonsei University College of Medicine, Seoul, 03722, Korea.
Yuki HayashiDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Shumei SongDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Elena ElimovaDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Jeannelyn S EstrallaDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Jeffrey H LeeDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Manoop S BhutaniDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Yiling LuDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Wenbin LiuDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Jeeyun LeeDepartment of Medicine, Samsung Medical Center, Division of Hematology-Oncology, Gangnam-Gu, Seoul, 06351, Korea.
Won Ki KangDepartment of Medicine, Samsung Medical Center, Division of Hematology-Oncology, Gangnam-Gu, Seoul, 06351, Korea.
Sung KimDepartment of Surgery, Samsung Medical Center, Gangnam-Gu, Seoul, 06351, Korea.
Sung Hoon NohDepartment of Surgery, Yonsei University College of Medicine, Seoul, 03722, Korea.
Gordon B MillsDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Seon-Young KimPersonalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Korea.ORCID http://orcid.org/0000-0002-1030-7730
Jaffer A AjaniDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Ju-Seog LeeDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA. jlee@mdanderson.org.ORCID http://orcid.org/0000-0002-5666-9753
The University of Texas MD Anderson Cancer Center · USKorea University · KRYonsei University · KRKorea Research Institute of Bioscience and Biotechnology · KRKosin University · KRInha University · KRSamsung Medical Center · KRUlsan College · KR

Funding

Functional Proteomics by Reverse Phase Protein Array in CancerR50CA221675 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LU, YILING · 2017 to 2021
$726k
NCI NIH HHS R50 CA221675
6 · The paper itself

Abstract

Gastric cancer is a heterogeneous cancer, making treatment responses difficult to predict. Here we show that we identify two distinct molecular subtypes, mesenchymal phenotype (MP) and epithelial phenotype (EP), by analyzing genomic and proteomic data. Molecularly, MP subtype tumors show high genomic integrity characterized by low mutation rates and microsatellite stability, whereas EP subtype tumors show low genomic integrity. Clinically, the MP subtype is associated with markedly poor survival and resistance to standard chemotherapy, whereas the EP subtype is associated with better survival rates and sensitivity to chemotherapy. Integrative analysis shows that signaling pathways driving epithelial-to-mesenchymal transition and insulin-like growth factor 1 (IGF1)/IGF1 receptor (IGF1R) pathway are highly activated in MP subtype tumors. Importantly, MP subtype cancer cells are more sensitive to inhibition of IGF1/IGF1R pathway than EP subtype. Detailed characterization of these two subtypes could identify novel therapeutic targets and useful biomarkers for prognosis and therapy response.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic AgentsCell Line, TumorChemotherapy, AdjuvantDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleGastrointestinal Stromal TumorsHeterograftsHumansKaplan-Meier EstimateMesodermMice, Inbred BALB CMicrosatellite InstabilityMutationAntineoplastic AgentsReceptor, IGF Type 1

Identifiers

PMID29725014
PMCPMC5934392
OpenAlexW2802285660

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.