Evidence map›Paper›PMID 30054295›Full record

ArticleBlood2018

Oncogenic activation of the STAT3 pathway drives PD-L1 expression in natural killer/T-cell lymphoma.

Tammy Linlin Song, Maarja-Liisa Nairismägi, Yurike Laurensia, Jing-Quan Lim, Jing Tan, Zhi-Mei Li, Wan-Lu Pang, Atish Kizhakeyil, Giovani-Claresta Wijaya, Da-Chuan Huang and 19 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 207 papers.

0numbers the graph read from it
0cells of the map it votes in
207citing papers in PubMed
24.6field-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

207 citing papers in PubMed, 316 citations in OpenAlex.

  1. Journal for immunotherapy of cancer · 2025
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  17. A Masked Intruder: Extranodal Natural Killer/T-Cell Lymphoma Mimicking Preseptal Cellulitis.Mayo Clinic proceedings. Innovations, quality & outcomes · 2026
    Article
  18. Article
  19. Article
  20. Review

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

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

29 authors at 9 institutions in 4 countries.

Tammy Linlin SongLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.ORCID 0000-0002-2379-4101
Maarja-Liisa NairismägiLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Yurike LaurensiaLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Jing-Quan LimLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Jing TanLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Zhi-Mei LiLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore.
Wan-Lu PangLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Atish KizhakeyilLee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
Giovani-Claresta WijayaLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore.
Da-Chuan HuangLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Sanjanaa NagarajanLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore.
Burton Kuan-Hui ChiaLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Daryl CheahLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Yan-Hui LiuDepartment of Pathology, Guangdong General Hospital, Guangdong Academy of Medical Science, Guangzhou, China.
Fen ZhangDepartment of Pathology, Guangdong General Hospital, Guangdong Academy of Medical Science, Guangzhou, China.
Hui-Lan RaoState Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Tiffany TangDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.ORCID 0000-0003-3550-7111
Esther Kam-Yin WongLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.
Jin-Xin BeiState Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Jabed IqbalDepartment of Anatomical Pathology, Division of Pathology, Singapore General Hospital, Singapore.ORCID 0000-0003-4137-1791
Nicholas-Francis GrigoropoulosDepartment of Haematology, Singapore General Hospital, Singapore.
Siok-Bian NgDepartment of Pathology, Yong Loo Lin School of Medicine, and.ORCID 0000-0001-6051-6410
Wee-Joo ChngNational University Cancer Institute of Singapore, Singapore.ORCID 0000-0003-2578-8335
Bin-Tean TehLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore.
Soo-Yong TanDepartment of Pathology, Yong Loo Lin School of Medicine, and.
Navin Kumar VermaLee Kong Chian School of Medicine, Nanyang Technological University, Singapore.ORCID 0000-0002-5940-6633
Hao FanBioinformatics Institute, A*STAR, Singapore.ORCID 0000-0003-0199-9752
Soon-Thye LimLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.ORCID 0000-0002-0366-5505
Choon-Kiat OngLymphoma Genomic Translational Research Laboratory, Division of Medical Oncology, and.ORCID 0000-0001-6402-4288
National Cancer Centre Singapore · SGSun Yat-sen University · CNAgency for Science, Technology and Research · SGDuke-NUS Medical School · SGGuangdong General Hospital · CNNanyang Technological University · SGSingapore General Hospital · SGYong In University · KRNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mature T-cell lymphomas, including peripheral T-cell lymphoma (PTCL) and extranodal NK/T-cell lymphoma (NKTL), represent a heterogeneous group of non-Hodgkin lymphomas with dismal outcomes and limited treatment options. To determine the extent of involvement of the JAK/STAT pathway in this malignancy, we performed targeted capture sequencing of 188 genes in this pathway in 171 PTCL and NKTL cases. A total of 272 nonsynonymous somatic mutations in 101 genes were identified in 73% of the samples, including 258 single-nucleotide variants and 14 insertions or deletions. Recurrent mutations were most frequently located in

Indexed as

Gene Expression Regulation, NeoplasticMutation, MissenseSignal TransductionAmino Acid SubstitutionB7-H1 AntigenCell Line, TumorHumansLymphoma, Extranodal NK-T-CellNeoplasm ProteinsSTAT3 Transcription FactorB7-H1 AntigenCD274 protein, humanNeoplasm ProteinsSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID30054295
PMCPMC6148343
OpenAlexW2622400061

What OpenQuestion holds

Textmetadata
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.