Evidence map›Paper›PMID 12096347›Full record

ArticleOncogene2002

Frequent mutations of Fas gene in nasal NK/T cell lymphoma.

Tetsuya Takakuwa, Zhiming Dong, Shinichi Nakatsuka, Shizuo Kojya, Yasuaki Harabuchi, Woo-Ick Yang, Shigekazu Nagata, Katsuyuki Aozasa

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. The broad and challenging landscape of extranodal lymphoproliferations.Virchows Archiv : an international journal of pathology · 2020
    Review
  8. Efficient recruitment of c-FLIPCancer science · 2020
    Article
  9. Review
  10. Review
  11. Navigating the Fas lane to improved cellular therapy for cancer.The Journal of clinical investigation · 2019
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Cutaneous EBV-related lymphoproliferative disorders.Seminars in diagnostic pathology · 2017
    Article
  18. Molecular Pathogenesis of Peripheral T Cell Lymphoma.Current hematologic malignancy reports · 2015
    Review
  19. Article
  20. Article
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

8 authors at 4 institutions in 2 countries.

Tetsuya TakakuwaDepartment of Pathology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Zhiming Dong
Shinichi Nakatsuka
Shizuo Kojya
Yasuaki Harabuchi
Woo-Ick Yang
Shigekazu Nagata
Katsuyuki Aozasa
Osaka University · JPAsahikawa Medical College Hospital · JPUniversity of the Ryukyus · JPYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fas (Apo-1/CD95) is a cell-surface receptor involved in cell death signaling through binding of Fas ligand. Mutation of Fas gene in lymphoid cells results in accumulation of these cells, which might thus contribute to lymphomagenesis. We examined the open reading frame of Fas cDNA in 14 cases of nasal NK/T-cell lymphoma. Mutations of Fas gene were detected in seven (50%) of 14 cases which comprised four frameshift, two missense, and one silent mutations. Frameshift mutations were caused by insertion of 1 bp (A) at nucleotide 1095 in two cases and by deletion of 1 bp at nucleotide 597 and at 704, respectively, in one each. Mouse T-cell lymphoma cells transfected with two missense mutated genes and frameshift mutations caused by insertion of 1 bp (A) at nucleotide 1095 were resistant to apoptosis induced by the anti-Fas antibody. These findings suggested that accumulation of lymphoid cells with Fas mutations provides a basis for the development of nasal NK/T-cell lymphoma.

Indexed as

ApoptosisDNA Mutational Analysisfas ReceptorFlow CytometryGenetic Predisposition to DiseaseGranuloma, Lethal MidlineHumansKiller Cells, NaturalLymphoma, T-CellMutationRNA, Messengerfas ReceptorRNA, Messenger

Identifiers

PMID12096347
OpenAlexW2331316755

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.