Evidence map›Paper›PMID 38358347›Full record

ArticleCancer research communications2024

Establishment and Characterization of an Epstein-Barr Virus-positive Cell Line from a Non-keratinizing Differentiated Primary Nasopharyngeal Carcinoma.

Annie Wai Yeeng Chai, Shi Mun Yee, Hui Mei Lee, Norazlin Abdul Aziz, Pei San Yee, Marini Marzuki, Ka Wo Wong, Alan K S Chiang, Larry Ka-Yue Chow, Wei Dai and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2024. 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
3.7field-weighted citation impact, top 6% 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, 13 citations in OpenAlex.

  1. Pooled it
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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

20 authors at 8 institutions in 4 countries.

Annie Wai Yeeng ChaiTranslational Cancer Biology Research Unit, Cancer Research Malaysia, Malaysia.ORCID 0000-0002-8015-6050
Shi Mun YeeTranslational Cancer Biology Research Unit, Cancer Research Malaysia, Malaysia.ORCID 0009-0007-9858-1817
Hui Mei LeeTranslational Cancer Biology Research Unit, Cancer Research Malaysia, Malaysia.ORCID 0009-0001-3542-2639
Norazlin Abdul AzizMolecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Ministry of Health, Malaysia.ORCID 0000-0001-8137-2399
Pei San YeeTranslational Cancer Biology Research Unit, Cancer Research Malaysia, Malaysia.ORCID 0000-0002-6548-2149
Marini MarzukiMolecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Ministry of Health, Malaysia.ORCID 0000-0002-6992-8590
Ka Wo WongDepartment of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, P.R. China.ORCID 0009-0006-4042-7529
Alan K S ChiangDepartment of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, P.R. China.ORCID 0000-0002-1089-5325
Larry Ka-Yue ChowDepartment of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, P.R. China.ORCID 0000-0001-7448-5811
Wei DaiDepartment of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, P.R. China.ORCID 0000-0002-5558-0685
Teng Fei LiuSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, P.R. China.ORCID 0009-0000-8686-1749
Lu Ping TanMolecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Ministry of Health, Malaysia.ORCID 0000-0002-7934-2462
Alan Soo Beng KhooMolecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Ministry of Health, Malaysia.ORCID 0000-0002-8268-5271
Kwok Wai LoDepartment of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, P.R. China.ORCID 0000-0002-3488-6124
Paul V H LimTung Shin Hospital, Malaysia.ORCID 0009-0004-6571-3682
Pathmanathan RajaduraiSubang Jaya Medical Centre, Malaysia.ORCID 0000-0002-9199-1940
Howard LightfootWellcome Sanger Institute, Cambridge, United Kingdom.ORCID 0000-0003-2082-9986
Syd BarthorpeWellcome Sanger Institute, Cambridge, United Kingdom.ORCID 0009-0002-5155-0646
Mathew J GarnettWellcome Sanger Institute, Cambridge, United Kingdom.ORCID 0000-0002-2618-4237
Sok Ching CheongTranslational Cancer Biology Research Unit, Cancer Research Malaysia, Malaysia.ORCID 0000-0002-6765-9542
University of Hong Kong · HKCancer Research Malaysia · MYMinistry of Health · MYWellcome Sanger Institute · GBChinese University of Hong Kong · HKHospital Kuala Lumpur · MYMonash University Malaysia · MYUniversity of Malaya · MY

Funding

Medical Research Council MR/P013457/1Medical Research Council MR/V005936/1
6 · The paper itself

Abstract

Nasopharyngeal carcinoma (NPC), a cancer that is etiologically associated with the Epstein-Barr virus (EBV), is endemic in Southern China and Southeast Asia. The scarcity of representative NPC cell lines owing to the frequent loss of EBV episomes following prolonged propagation and compromised authenticity of previous models underscores the critical need for new EBV-positive NPC models. Herein, we describe the establishment of a new EBV-positive NPC cell line, designated NPC268 from a primary non-keratinizing, differentiated NPC tissue. NPC268 can undergo productive lytic reactivation of EBV and is highly tumorigenic in immunodeficient mice. Whole-genome sequencing revealed close similarities with the tissue of origin, including large chromosomal rearrangements, while whole-genome bisulfite sequencing and RNA sequencing demonstrated a hypomethylated genome and enrichment in immune-related pathways, respectively. Drug screening of NPC268 together with six other NPC cell lines using 339 compounds, representing the largest high-throughput drug testing in NPC, revealed biomarkers associated with specific drug classes. NPC268 represents the first and only available EBV-positive non-keratinizing differentiated NPC model, and extensive genomic, methylomic, transcriptomic, and drug response data should facilitate research in EBV and NPC, where current models are limited. SIGNIFICANCE: NPC268 is the first and only EBV-positive cell line derived from a primary non-keratinizing, differentiated nasopharyngeal carcinoma, an understudied but important subtype in Southeast Asian countries. This model adds to the limited number of authentic EBV-positive lines globally that will facilitate mechanistic studies and drug development for NPC.

Indexed as

Epstein-Barr Virus InfectionsNasopharyngeal NeoplasmsAnimalsCell Line, TumorHerpesvirus 4, HumanMiceNasopharyngeal Carcinoma

Identifiers

PMID38358347
PMCPMC10911800
OpenAlexW4391844966

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.