Evidence map›Paper›PMID 32004387›Full record

ArticleBritish journal of haematology2020

Evaluation of the PIK3 pathway in peripheral T-cell lymphoma and NK/T-cell lymphoma.

Dachuan Huang, Tammy Linlin Song, Maarja-Liisa Nairismägi, Yurike Laurensia, Wan-Lu Pang, Daryl Cheah Ming Zhe, Esther Kam Yin Wong, Giovani Giovani-Clarest Wijaya, Jing Tan, Sze Huey Tan and 10 more

Abstract read
In one paragraph

Article in British journal of haematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
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  12. Obesity and Risk for Lymphoma: Possible Role of Leptin.International journal of molecular sciences · 2022
    Review
  13. Article
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  15. Article
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  18. Update on the role of copanlisib in hematologic malignancies.Therapeutic advances in hematology · 2021
    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

20 authors.

Dachuan HuangLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.ORCID 0000-0002-7518-4081
Tammy Linlin SongLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.
Maarja-Liisa NairismägiLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.
Yurike LaurensiaLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.
Wan-Lu PangLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.
Daryl Cheah Ming ZheLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.
Esther Kam Yin WongLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.
Giovani Giovani-Clarest WijayaLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore City, Singapore.
Jing TanLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore City, Singapore.
Sze Huey TanDivision of Clinical Trials and Epidemiological Sciences, National Cancer Centre Singapore, Singapore City, Singapore.ORCID 0000-0002-3089-7379
Jing-Quan LimLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.ORCID 0000-0003-3732-8707
Burton Kuan Hui ChiaLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.ORCID 0000-0003-1554-4871
Jason Yongsheng ChanDivision of Medical Oncology, National Cancer Centre Singapore, Singapore City, Singapore.
Tiffany Pooi Ling TangDivision of Medical Oncology, National Cancer Centre Singapore, Singapore City, Singapore.
Nagavalli SomasundaramDivision of Medical Oncology, National Cancer Centre Singapore, Singapore City, Singapore.
Chee Leong ChengDepartment of Pathology, Singapore General Hospital, Singapore City, Singapore.ORCID 0000-0002-2140-4827
Oliver PolitzResearch & Development, Pharmaceuticals, Bayer AG, Leverkusen, Germany.
Ningshu LiuResearch & Development, Pharmaceuticals, Bayer AG, Leverkusen, Germany.
Soon Thye LimDivision of Medical Oncology, National Cancer Centre Singapore, Singapore City, Singapore.
Choon Kiat OngLymphoma Genomic Translational Research Laboratory, Division of Cellular & Molecular Research, National Cancer Centre Singapore, Singapore City, Singapore.ORCID 0000-0001-6402-4288

Funding

LING Foundation (NRDUKSN18101)National Medical Research Council of Singapore MOHIAFCat1-11015National Medical Research Council of Singapore NMRC-OFIRG16NOV090New Century Foundation (NCCRF-YR2014-SEP-SD2)Pharmaceuticals, Bayer AGTANOTO Foundation (NRDUKST18101)
6 · The paper itself

Abstract

Peripheral T-cell lymphomas (PTCL) and natural killer (NK)/T-cell lymphomas (NKTCL) are a heterogeneous group of aggressive malignancies with dismal outcomes and limited treatment options. While the phosphatidylinositol 3-kinase (PIK3) pathway has been shown to be highly activated in many B-cell lymphomas, its therapeutic relevance in PTCL and NKTCL remains unclear. The aim of this study is to investigate the expression of PIK3 and phosphatase and tensin homolog (PTEN) in these subtypes of lymphoma and to identify potential therapeutic targets for clinical testing. Therefore, the expression of PIK3α, PIK3β, PIK3γ, PIK3δ and PTEN was analyzed in 88 cases of PTCL and NKTCL samples by immunohistochemistry. All PTCL and NKTCL samples demonstrated high expression of PIK3 isoforms. In particular, high PIK3α expression was significantly associated with poor survival, even after adjustment for age, International Prognostic Index (IPI) score and anthracycline-based chemotherapy in first line. Notably, copanlisib, a pan-class I inhibitor with predominant activities towards PIK3α and PIK3δ isoforms, effectively inhibited phosphorylation of AKT, 4E-BP-1 and STAT3, causing G

Indexed as

Cell ProliferationFemaleHumansLymphoma, T-Cell, PeripheralMaleMiddle AgedNatural Killer T-CellsPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasecopanlisibNK/T-cell lymphomaperipheral T-cell lymphomaphosphatidylinositol 3-kinasePI3K

Identifiers

PMID32004387
PMCPMC7322801

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.